Host Impairments in Patients with Neoplastic Diseases
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Healthy individuals possess an immune system comprising physical barriers, innate and acquired immunity as well as the indigenous microflora that populate the body surfaces. The immune system maintains constant vigilance over the body at the cellular level as well as at the interface between the host integument and the resident microflora. However, neoplastic diseases and their treatment often lead to impaired immunity resulting in an increased risk of infections due to viruses, bacteria, fungi, and protozoa. This chapter explores the various aspects of host impairment focusing on the components of immunity and the interplay between them to explain why it is that these patients succumb to infections per se. In so doing, we hope that the reader will be better equipped to understand the risks patients face so as to anticipate potential infectious complications and implement appropriate measures to help attain successful remission of the neoplastic diseases and maintain the best quality of life for the patient.
KeywordsInnate immunity Commensal flora Natural antibiotics Neutropenia Humoral immunity Cellular immunity Host defenses Mucosal barrier injury Mucositis Infectious complications
In the course of evolution, nature has provided the normal human individual with an impressive and effective defense system against microbial enemies. On its own, the normal defense system recognizes foreign invaders, alerts the relevant protective mechanisms, launches counterattacks, ceases hostilities as soon as the job is done, and clears up the battlefield, causing only negligible collateral damage. An intact immune system offers protection against most microbial aggressors through a complex interrelationship of protecting surfaces, cells, and soluble factors.
2 Basic Clinical Condition and Organ Function
2.1 Nutritional Status
Weight loss correlates inversely with survival in patients with cancer. This occurs whether or not intensive treatment is given because the integrity of host defenses can be endangered by the catabolic state induced by cachexia and malnutrition, resulting in a quantitatively deficient intake of calories and protein, with insufficient vitamin levels and trace metal concentrations [2, 3]. Cachexia will be exacerbated by anorexia, chemotherapy-induced nausea and vomiting, gastrointestinal obstructions, as well as by metabolic disturbances. These perturbations may result in delayed tissue healing, mucosal atrophy with a decrease in the secretions of lysozyme and secretory IgA, as well as impairment of both the classical and alternative complement pathways. Vitamin A deficiency may also have a detrimental effect on the cellular immune system .
Deficiencies in trace elements can further undermine the host defenses on already compromised patients. Zinc deficiency can develop during total parenteral nutrition disturbing the function of phagocytes and T cells but can be overcome by adding the mineral . The microbicidal capacity in vitro of neutrophils and T-lymphocyte function is reduced by iron deficiency though the clinical significance is uncertain. Iron overload occurring in the setting of hematopoietic stem cell transplantation (HSCT) is a risk factor for infection involving a variety of pathogens such as Yersinia enterocolitica, Listeria monocytogenes, Vibrio spp., Plasmodium falciparum, Mycobacterium tuberculosis, Mycobacterium avium complex, Candida albicans, Aspergillus spp., and the agents of mucormycosis . A deficit in phosphate, which may occur during episodes of starvation and insufficient parenteral nutrition, is associated with a decrease in the chemotactic, phagocytic, and microbicidal functions of granulocytes in vitro, and clinically with bacterial and fungal infections .
Concomitant chronic illnesses, such as chronic pulmonary diseases or renal and hepatic failure, enhance the risk of infection. Patients with a preexisting immune disturbance, such as HIV infection or a congenital immunodeficiency syndrome, are placed in double jeopardy. Much more common, however, is the detrimental effects of smoking, particularly in patients with primary lung tumors, due to airway colonization with pathogenic microorganisms and impaired clearance of secretions . Tobacco use is also a risk factor for infection in autologous HSCT recipients .
Patients with poorly controlled diabetes mellitus are more likely to develop wound infections after skin penetration injuries, and they frequently suffer from concurrent vascular disease and neuropathy. High concentrations of glucose in the urine, and oral secretions promote colonization by Candida spp. and other pathogens . There is a well-known association between diabetes mellitus and notorious infections, such as rhinocerebral mucormycosis and malignant external otitis , which is not difficult to explain in view of the immune aberrations that are associated with diabetes, such as impaired opsonization, decreased chemotactic activity of granulocytes and monocytes, iron overload , and myeloperoxidase deficiency .
2.3 Physiologic Status
Tumors themselves may also predispose to infection by local organ dysfunction. In patients with solid tumors, obstruction of natural passages can lead to inadequate drainage of secretory or excretory fluids from nasal sinuses, bronchi, and bile ducts. Furthermore, tissue invasion may create connections between normally sterile spaces and the environment through disruption of epithelial surfaces. Examples include perforation of the esophagus by mediastinal tumors, invasive gynecologic malignancies with local pelvic abscesses, skin ulcerations with cellulitis and deep soft-tissue infections, and invasion of the bowel wall by tumors with the lower gastrointestinal tract, resulting in bacteremia. Localizations in the central nervous system, spinal cord compression, and paraneoplastic neuropathy are associated with an increased risk of infection due to lethargy and, for instance, a diminished ability to cough and swallow, and incomplete emptying of the bladder .
Of course, in hematologic malignancies, infectious complications invariably go hand in hand because the neoplasm resides within the immune system itself and interferes directly and indirectly with its function. Patients undergoing splenectomy have a risk of around 1 in 20 of that they will develop overwhelming sepsis at some time during their life. Encapsulated bacteria such as Streptococcus pneumoniae and Haemophilus influenzae are usually the culprits, though Neisseria meningitidis and staphylococci are occasionally encountered.
Several factors might explain this increased susceptibility to microbial infection. Encapsulated bacteria are able to elude phagocytosis because specific opsonizing antibodies are necessary for efficient phagocytosis. The spleen is also the principal organ for eliminating particles that are not opsonized, and so, it is left to the macrophages within the organ to remove them. The primary immunoglobulin response also takes places in the spleen, and low levels of circulating IgM have been observed after splenectomy and in cases of functional asplenia.
2.4 Psychologic Status
Psychologic stress is thought to suppress host defense mechanisms. This general assumption has been corroborated by the observations that psychologic stress has a negative influence on the function of T cells and NK cells. Indeed, stress and the amount of stress appear to be associated with an increased risk of acute viral respiratory illness. This is most likely mediated by endogenous opioids, hormones from the hypothalamic–pituitary–adrenal axis, catecholamines, and cytokines .
In elderly patients, the atrophy and dryness of the skin and mucosal membranes may lead to increased susceptibility to infections. In addition, the primary and secondary humoral responses, as well as the oxidative metabolism of neutrophils and T-cell functions, decline with age, but their exact role in susceptibility to infection is unclear .
3 Integument and Commensal Microflora
The integument comprises the skin, respiratory tract, (including the nasal cavity, ears, and conjunctiva), the alimentary tract, and the genitourinary tract and provides the first line of defense against microbial invasion. In physical terms, the only difference between the skin and the other parts of the integument is that it is dry, whereas the others are bathed in mucins and therefore continually moist. Thus, while both surfaces are normally colonized with a variety of microorganisms, including many different genera of bacteria and yeasts, the range and number of species and the biomass associated with mucosal surfaces are much greater than those of the skin. However, the resident microbial flora of each surface play an integral role in helping to maintain the function and integrity of these first lines of defense. Moreover, when intact and healthy, both the mucosa and skin are capable of resisting colonization with foreign or allochthonous organisms, thus maintaining an ecologic balance within the indigenous microbial flora.
The skin of an adult has an estimated surface area of 1.5–2.3 m2 and possesses features that are inimical to microbial invasion, provided it remains healthy and intact. The cells are composed of keratin and resemble loose paving stones. They are joined together by desmosomes and are continually sloughed off during desquamation so that adherent bacteria are also lost. This rapid cell turnover occurs every 2 weeks and helps to limit opportunities for transient organisms to establish residence.
Microbial residents of the normal skin
Many of the resident bacteria also elaborate toxins that inhibit closely related microorganisms, allowing individual species to retain their foothold and consolidate their territory. Resident species also grow as biofilms, which consist of microcolonies enmeshed in a glycocalyx, rather than the planktonic growth found in laboratory cultures. Thus, each microbial consortium possesses a boundary and exists as a distinct unit separate from its neighbors.
3.1.1 Erosion of the Skin Integument, Including Intravenous Catheters
The effectiveness of the skin as a defense barrier can be eroded in a variety of ways. Topical antibiotics and those secreted in sweat will disturb the balance within the resident commensal flora, leaving the surface vulnerable to colonization by exogenous potential pathogens such as the gram-negative bacteria. Antibiotics will also exert selective pressure on the resident flora, causing resistance to emerge, as has been observed during treatment with ciprofloxacin because the drug is secreted with sweat . Chemotherapy and irradiation can bring about radical changes in the normal skin by interrupting normal cell replacement, resulting in hair loss, dryness, and loss of sweat production. The latter may also lead to lower levels of the antimicrobial peptide, dermcidin, which is secreted in normal sweat and is an effector of innate immunity . In addition, steroids also can exert a profound effect on sebum secretions. When the skin is broken, the release of fibronectin is thought to assist colonization with Staphylococcus aureus, and other changes facilitate colonization with gram-negative bacilli such as Acinetobacter baumanii and Enterobacteriaceae. Cutaneous infection results from the loss of integrity and reduced local immunity of the skin as well as disturbances within the resident flora. Abraded skin and the associated exudates and minor breaches in the integument can lead to local infection as well as provide a reservoir that assists further spread to other body surfaces, including the oral cavity. When the balance is lost between the host defenses and resident commensal flora around the hair follicles, they can become inflamed and necrotic, forming a potential nidus of infection.
Cutaneous infections in the immunocompromised patient can also develop from needle punctures, but the insertion of catheters provides the single most effective means of breaching the natural protective barrier of the skin and creating access for microorganisms.
3.2 Upper Respiratory, Alimentary, and Genitourinary Tracts
The surface area of the upper respiratory, alimentary, and genitourinary tracts available for microbial colonization is greater than that afforded by the skin because of the folds, crypts, and villi. The surfaces of each anatomic region are also very different, ranging from the hard enamel of the teeth to the microvilli of the bowel. Extreme changes in the local environment also occur, ranging from the neutrality of the mouth to the acidity of the stomach. Although the interplay between these environments and their resident microflora is incomplete and poorly understood, some generalizations are possible and useful in understanding how the mucosal surfaces play their part as a first line of defense.
Two principal physical host factors influence the microbial ecology of the mucosal surfaces. Dilution of the microbial load is achieved by sneezing and coughing of microbes trapped in mucus, flushing of the mouth and esophagus by saliva, micturition, and peristalsis of the intestines. Acidity plays a crucial role both in disinfecting the stomach and in regulating the microbial milieu of the vagina. The upper respiratory, alimentary, and genitourinary tracts are essentially composed of epithelial cells interspersed by cells that produce mucins. These hydrophilic substances perform various functions, including lubrication, waterproofing, and preventing sudden changes in osmotic pressure . They also contain inhibitory substances, such as lactoferrin, lysozyme, defensins, and peroxidase, as well as secretory IgA. Mucins also appear to interfere with adherence of foreign bacteria to epithelial cells and prevent access of antigens to antibodies while allowing the biofilm formed by resident bacteria to blend or fuse so that the bacteria can form a more intimate contact with the epithelial cells.
Resident flora of the upper respiratory tract and oral cavity
Streptococcus spp. nonhemolytic group
Streptococcus spp. viridans group
S. oralis, S. mitis
3.2.1 The Lung
The lung appears to be particularly vulnerable to damage by cytotoxic chemotherapy and irradiation and is exquisitely susceptible to infection. Immunopathologic reactions mediated by the pulmonary macrophages that survive chemotherapy can lead to various other syndromes, including respiratory distress. Pulmonary hemorrhage as a result of profound thrombocytopenia further imperils the lung, increasing the risk of infection. However, the risk of invasion and dissemination is high when the integrity of the mucosa is impaired, the ecology of resident flora is disturbed, and exogenous microorganisms such as gram-negative bacilli or other potential pathogens establish colonization. Resident flora such as Candida spp. can result in superficial infection, often as a consequence of reactivation of herpes simplex virus [19, 20]. Clinically, the presence of pseudomembranes over the ulcerated tissue can initiate local invasion and progressive spread to the esophagus and gastrointestinal tract, resulting in disseminated candidiasis. Aspiration and inhalation of spores and hyphal elements of Aspergillus spp. and other molds permit colonization of the sinuses and bronchial tree, which may extend into the alveolar spaces, resulting in invasive disease that is often fatal.
3.2.2 Microflora of the Intestinal Tract
Resident flora of the lower alimentary tract
Gram-negative anaerobic bacilli
Gram-positive anaerobic bacilli
C. tertium, C. difficile, C. sporogenes
E. faecalis, E. faecium
S. milleri, S. mitis, S. oralis,
Gram-positive anaerobic cocci
Gram-positive anaerobic cocci
C. albicans, C. glabrata, C. krusei, C. lusitania
Normally, the alimentary tract flora contains in excess of 1014 microorganisms, representing between 500 and 1,000 different species  and amounting to several grams, but only very few species are capable of establishing infection, even in the most profoundly immunosuppressed patient. Most of the microbial flora is densely distributed around the surfaces of the oral cavity and the large bowel, where scores of different microorganisms, including spirochetes, spore formers, bacilli, and cocci, compete for the available surfaces and nutrients. Anaerobes predominate and play a crucial role in maintaining a healthy commensal flora, preventing the establishment of exogenous or allochthonous organisms, which is known as colonization resistance [25, 26]. The integrity of the mucosa, the production of saliva and mucus, peristalsis, gastric pH, bile acids, digestive enzymes, and the levels of secretory IgA also play an important role in maintaining colonization resistance .
3.3 Impact of Antimicrobial Agents on Colonization Resistance of the Alimentary Tract
Exposure to antimicrobial agents is one of the most effective means for destroying colonization resistance, as is manifest by fungal overgrowth and increases in the enterococcal populations [28, 29, 30]. The most likely contributors to colonization resistance, the gram-positive non-spore forming, lactic acid-producing bacilli, particularly bifidobacteria, are particularly susceptible to antibiotics known to impair colonization resistance, including the penicillins, rifamycin, clindamycin, erythromycin, bacitracin, and vancomycin [24, 27, 31, 32, 33, 34, 35, 36]. Some cephalosporins are also detrimental to colonization resistance, whereas meropenem and the quinolones have been declared “friendly” [28, 34, 35, 36, 37, 38, 39]. Some drugs such as aztreonam and imipenem only appear “friendly” because they are inactivated by feces [30, 40], whereas under the circumstance of diarrhea, parenteral feeding, and gut toxicity, normal stool is no longer produced so these agents may remain sufficiently active to destroy what remains of the colonization resistance. Initially, co-trimoxazole was thought to be neutral [27, 34, 41, 42, 43, 44, 45], but other evidence suggests otherwise . Individual antibiotics that appear to spare colonization resistance, such as ceftazidime and piperacillin, might have a marked impact when given in combination, leading to an increase in both Clostridium difficile as well as yeasts . C. difficile can cause enterocolitis, which responds to treatment with metronidazole or oral vancomycin, but the latter may select for resistant bacteria such as Enterococcus faecium and Lactobacillus rhamnosus . The widespread use of fluoroquinolones for prophylaxis has led to the emergence of resistance among the E. coli, which are indigenous to the bowel [49, 50, 51, 52].
4 Innate Immunity
The immune system has historically been divided into the innate (“natural”) and adaptive (“acquired”) immune system to highlight the difference in primary primitive versus secondary more sophisticated responses. Current knowledge, however, challenges this dichotomy because the innate and adaptive immune systems have considerable overlap and are highly interlinked. For instance, the composition of the “cytokine cocktail” released after stimulation of pattern recognition receptors (PRRs) by pathogen-associated molecular patterns (PAMP) directs the adaptive immune response toward T-helper 1 (Th1), Th2, Th17, or regulatory T-cell activity . In other words, the innate immune system orchestrates the adaptive immune system [53, 54]. Nevertheless, for the sake of clarity, the dichotomy has been maintained so far.
The innate immune system is a primary highly conserved immune system that can been found in most living organisms, from plants to insects to mammals . This is essentially all there is to the immune system of plants and insects unlike more evolved creatures such as mammals that also possess an adaptive immune response. Being the first point of contact with microorganisms and foreign molecules, the innate immune system mobilizes a primary response to external threats. This is characterized by being rapid, crude, lacking in specificity and without any development of “memory” so that when re-challenged the same response ensues. By contrast, the adaptive immune system is highly specific in recognizing foreign molecules and reacts with increased magnitude with every re-challenge.
The innate immune system consists of a variety of humoral and cellular components  as well as the epithelial cell network that creates a direct physical barrier. Humoral factors consist of the complement systems (classical, alternative, and lectin pathway), antimicrobial peptides (AMPs), acute phase proteins (e.g., C-reactive protein), and mucosal secretions (mucins and saliva). Cellular components consist of natural killer cells (NK) and phagocytic cells such as monoyctes, macrophages, polymorphonuclear neutrophils (PMN), and dendritic cells (DC). Endothelial cells and fibroblasts are also being increasingly recognized as essential cellular components of the innate immune system. For instance, intestinal epithelial cells (IECs) recognize microbes, produce cytokines and AMPs, phagocytize and present antigens .
4.1 Pattern Recognition Receptors: Key Players of the Innate Immune System
The discovery of a pattern recognition receptor (PRR, the so-called Toll receptor) in the fruit fly helped reveal just how innate immune cells recognize foreign molecules. It also boosted research into innate immunity, which lead to the discovery of many different PRRs in humans, including the Toll-like receptors (TLRs), the NOD-like receptors (NLRs), and the family of C-type lectin receptors (CLRs) [57, 58, 59].
PRRs recognize conserved molecular patterns of the cell wall of bacteria, or the so-called PAMPs, including lipids, proteins, and nucleic acids. PRRs are expressed on nearly every human cell ranging from blood cells to epithelial and endothelial cells. They are present on the cell surface though some reside in the cytosol. The expression is highly regulated with an increase in expression during infection and other inflammatory conditions. These receptors are capable of recognizing PAMPs with a degree of specificity. Because microbes contain different motifs that are recognized by different PRRs, the system is redundant, thereby reducing the risk of infection when there is any dysfunction of certain PRRs.
Although originally PRRs were thought to discriminate self from nonself, they also recognize endogenous ligands, such as heparin sulfate, fibrinogen, heat shock proteins, and β-defensin-2, so-called danger-associated molecular patterns (DAMPs), released mostly in case of tissue damage [60, 61]. This enables the innate immune system to respond to danger, whether or not resulting from infection .
During infection and tissue damage, the ensemble of activated PRRs and subsequently activated intracellular signaling pathways results in the release of a mixture of cytokines and activation of diverse signaling pathways. The cytokine profile then defines the inflammatory response and orchestrates the development of the adaptive immune response, adequately controlling the infection while preventing uncontrolled inflammation and tissue damage [63, 64]. The simultaneous activation of multiple PRRs provides virtually an infinite range of possibilities for tailoring an effective response to a wide range of microbes. However, overwhelming infection, deregulated expression or activation of PRRs, and failing negative feedback mechanisms can result in disruption of this finely tuned immune system, resulting in infections or uncontrolled inflammatory responses manifesting as autoimmune diseases and sometimes systemic inflammatory response syndrome (SIRS) and acute respiratory distress syndrome (ARDS) [63, 65].
4.2 Antimicrobial Peptides: Nature’s Antibiotics
Antimicrobial peptides are evolutionarily conserved elements of innate immunity and probably originated because of the coevolution of host and pathogens, necessitating a strict control of pathogenic microbes while preserving beneficial commensal bacteria. More than 700 AMPs have been identified, and they are widely distributed in nature . In general, AMPs are small (12–50 amino acids), and amphipatic, and they contain two positive charges. AMPs are produced mainly by epithelial cells and PMNs. They can be constitutively expressed or inducible by microbial cell wall constituents, tissue damage, and pro-inflammatory cytokines.
AMPs possess pleiotropic functions in the context of host immunity, although not all AMPs share the same set of activities [66, 67]. Direct antimicrobial activity is related to the charge and amphipatic nature of the peptides, hydrophilic at one end and hydrophobic at the other end, facilitating interaction with the microbial cell membrane and ultimately resulting in pore formation and subsequent cell death . Other mechanisms of action have been described for these peptides including increased microbial clearance by opsonization and increased chemotaxis and activation of phagocytic cells. Other immunomodulatory activities have been described such as increased production of cytokines by stimulating PRRs, increased chemotaxis, reduced apoptosis in PMNs, and increased differentiation, maturation, and antigen presentation of DCs [66, 67, 68].
4.3 Cellular Components
4.3.1 Epithelial Cells: A Physical and Immunologic Barrier
The best-known defense function of epithelial cells is the creation of physical barriers. However, these cells are, in fact, “non-classical” immune cells as they are equipped with receptors that sense their surroundings and direct immune activity. Epithelial cells produce a wide array of mediators including antimicrobial peptides, growth factors, chemokines, and cytokines (IL-1 alpha, IL-7, IL-8, and IL-18). In addition, these cells can act as antigen-presenting cells. Moreover, they have immune regulatory functions as they communicate with B-lymphocytes, γδ-T lymphocytes, and dendritic cells. For instance, through the release of TGF-β, TSLP, and retinoic acid, epithelial cells contribute to the induction of tolerogenic dentritic cells and down-regulation of inflammation in environments that are constantly exposed to foreign antigens and the commensal flora.
Causes and sequelae of thrombocytopenia and thrombocytopathy
Causes of thrombocytopenia
Leukemia and lymphoma, bone marrow metastasis
Causes of thrombocytopathy
Leukemia and myeloma, renal insufficiency
Chemotherapy, β-lactam antibiotics, anti-inflammatory drugs, anti-histamines, heparin
Hemorrhagic lesions facilitate growth of microorganisms and interfere with organ function
Decrease of platelet-derived growth factor, epidermal cell growth factor, endothelial cell growth factor, fibronectin (diminished adhesion), P-selectin (diminished transmigration)
Under normal circumstances, the proliferation of neutrophil precursors is regulated by hematopoietic growth factors such as interleukin-3, granulocyte macrophage-colony stimulating factor (GM-CSF), and granulocyte-colony stimulating factor (G-CSF). Starting from a pluripotent stem cell, it takes approximately 6 days to form metamyelocytes by sequential divisions and another 6 days to mature into polymorphonuclear granulocytes . Approximately 90 % of the total population of neutrophils resides in the bone marrow, only to be released into the circulation upon an inflammatory stimulus. Neutrophils that enter the bloodstream are distributed over two compartments of equal size in dynamic equilibrium: a free circulating pool of neutrophils and the marginating pool, consisting of neutrophils that adhere loosely to the vascular endothelium. The size of these respective pools is under the influence of several factors.
Adherence of neutrophils to endothelial cells is mediated by a number of adhesion molecules on neutrophils, which are induced by factors such as complement factor C5a, which acts as a ligand. Likewise, there is a whole series of adhesion molecules on the endothelial cells themselves, with cytokines such as interleukin-1 and tumor necrosis factor-α being important inducers of these molecules . Other inflammatory impulses and glucocorticosteroids are also potent inhibitors of margination. Circulating neutrophils disappear after approximately 6 h in blood, whereas they survive 1–3 days in tissues.
During an acute inflammatory reaction, an increase in neutrophils, sometimes accompanied by eosinophils and followed by macrophages, can be seen at the site of inflammation. The formation of this inflammatory exudate is the result of activation of several humoral factors, such as cytokines, prostaglandins, and complement, which enhance the blood flow and increase vascular permeability. This occurs in conjunction with chemotactic activity, which results from other soluble factors, especially C5a, leukotriene B, interleukin-8, and bacterial products. In the peripheral blood, granulocytosis evolves as a consequence of the release of the marrow reserve and increased granulocytopoiesis on stimulation by factors such as interleukin-1. However, the mere presence of granulocytes at the site of an infection is meaningless if they are not able to execute their normal functions. Phagocytosis, an Fc- and C3b receptor-mediated process with IgG1, IgG3, and C3b as ligands or opsonins, results in the uptake of particles larger than one micron via pseudopods until they enclose in a vacuole (phagosome). The rate of ingestion by neutrophils is impressive in comparison with that of other phagocytes.
As soon as the particles, with or without opsonins, make contact with the cell membrane of a granulocyte, oxidases in the membrane are triggered to activate oxygen-dependent microbicidal mechanisms, and superoxide, hydrogen peroxide, and hydroxyl radicals are formed. During and after ingestion, the lysosomes, which are microscopically visible as azurophilic granules, fuse with the phagosome and pour their digestive enzymes into the vacuole, a process known as degranulation. One of these lysosomal enzymes, myeloperoxidase, triggers the reaction of H2O2 with chloride, which results in the formation of hypochlorite, a potent microbicidal product. Usually, this operation of phagocytosis and intracellular killing of microorganisms is a suicidal act for the neutrophils, leaving the remainder for consumption and enzymatic digestion by the more powerful macrophages. However, even macrophages may require cooperation with products from activated T lymphocytes for the optimal killing of some microorganisms.
The proliferation and maturation of eosinophilic precursors are under the control of interleukin-3, GM-CSF, and interleukin-5 and have a time span similar to that of neutrophils , whereas survival in the tissues appears to be considerably longer. Eosinophils are able to kill several parasites, largely by means of an extracellular process mediated by IgE and, probably, complement.
4.3.4 Monocytes and Macrophages
Monocytes (blood) and macrophages (tissue)
Monocytes and macrophages are cells of the myeloid lineage derived from the pluripotent myeloid progenitors under the influence of growth factors IL-3 and GM-CSF. Monocytes circulate in the peripheral blood, but enter peripheral tissues where they transform to more adapted macrophages, which patrol the barriers for invaders. Monocytes and macrophages are preeminently equipped in phagocytosis of microbial invaders, but also of cell debris, apoptotic cells, and foreign materials. Additionally, they can act as antigen-presenting cells, although less efficiently as DCs, and produce pro-inflammatory cytokines (M1-type macrophages). However, some macrophages (M2 type) also exhibit regulatory functions by releasing anti-inflammatory cytokines, such as IL-10.
4.3.5 NK Cells
NK cells were originally defined as immune cells naturally capable of killing specific tumor cell lines. They belong to the innate immune system, for they do not need aid with DCs and priming to be effective. These cells have been shown to be indispensible in inducing anti-viral and anti-tumor responses. NK cells are equipped with a complex set of surface molecules and receptors that are either activating (KARs) or inhibiting (KIRs) . The KIRS are very important because with these receptors NK cells can differentiate normal host cells from foreign or infected cells by differentiating between host cell expression of normal or altered MHC class I expression. Effector functions consist of direct cytotoxicity resulting from the release of perforin and granzyme, antibody-dependent cellular cytotoxicity, and release of cytokines, especially IFNγ. In addition, NK cells possess regulatory functions. At one side, they support DC maturation, Th1 cell activation, and release of pro-inflammatory cytokines, but at the other side, they kill activated T lymphocytes, hyper-activated macrophages, and immature DCs, dampening inflammation and shutting down immune response .
4.4 Innate Immunity and the Integument
The integument is normally in a state of immunologic tolerance and homeostasis despite being exposed to billions of microorganisms and other foreign substances such as food, beverages, and drugs. This clearly demands comprehensive and careful regulation of the immune system [76, 77]. There is a steady balance between tolerance to non-pathogenic commensal bacteria and intolerance to their pathogenic cousins, necessitating the generation of an effective immune response. Constant interaction and “cross talk” between IECs, immune cells (monocytes, macrophages, and DCs), and microbes are necessary to determine exactly what is going on at the epithelial surface and direct immune actions for maintaining the status quo [76, 78, 79]. Commensal and pathogenic bacteria are also kept in check, as are immune responses, to prevent damage and uncontrolled inflammation.
The innate immune system plays a central role in keeping this delicate balance and even small defects therein can result in disease as a result of infection or uncontrolled inflammation. Both PRRs and AMPs are of great significance here. During homeostasis, activation of PRRs such as TLR2 and TLR9, by commensal flora, helps to maintain barrier function and immune quiescence [80, 81, 82], whereas sensing of even commensal flora can elicit pro-inflammatory responses and contribute to the pathogenesis of diseases that compromise barrier functions, such as inflammatory bowel diseases [83, 84, 85, 86] AMPs like β-defensins are widely expressed in the skin and gastrointestinal tract and regulate the composition and burden of the microbial flora at these epithelial barriers.
5 Acquired Immunity
5.1 Humoral Immunity
The humoral branch of the immune system involves interaction of B cells with antigen and their subsequent proliferation and differentiation into antibody-secreting plasma cells. An important difference in antigen recognition by T cells and B cells is that the latter can recognize an antigen, whereas T cells can only do so once the antigen has been phagocytosed and is presented on the surface of an antigen-presenting cell. In this way, the immune system is able to cope with invaders under a variety of different circumstances. The humoral system recognizes a plethora of bacterial or viral microorganisms as well as the soluble proteins they release. The cell-mediated system is suited to recognizing altered cells belonging to the “self,” that is, infected phagocytes as well as cancer cells.
Immunoglobulins are produced by the humoral branch of the system when challenged by an antigen and bound to it. IgM is secreted early and during differentiation. Plasma cells then become committed to produce the other classes of immunoglobulin, such as IgG, IgA, IgE, and IgD . The specific functions of IgG and IgM include not only neutralization of the antigen, but also complement activation and opsonization. Secretory IgA, which is found on mucosal surfaces, is not an opsonin but it inhibits the motility of bacteria, neutralizes their toxins, and prevents their adherence to epithelial cells. Circulating IgA probably plays only a minor role in host defense.
The spleen plays an important role in the humoral immune response as the primary immunoglobulin response takes place there, as shown by the low concentrations of IgM found after splenectomy. Reduced concentrations of the complement factor properdin have also been found, leading to suboptimal opsonization. Functional asplenia develops in a large proportion of patients after allogeneic HSCT and is also associated with increased risk for bacterial infections.
5.2 Acquired Cellular Immunity
Whereas humoral immunity is primarily responsible for clearing extracellular bacteria, the cellular immune system serves also to eliminate intracellular pathogens and virus-infected cells.
5.2.1 Dendritic Cells
Dendritic cells have a specific role in immunity as they function at the crossroads of innate and acquired immunity. They arouse a keen interest because of their unique capacity to efficiently process antigens, present them, and sensitize naive T cells. By releasing different cocktails of cytokines, they shape T lymphocyte, and also B-lymphocyte and NK cell responses, functioning as orchestrators of acquired immunity. A wide range of dendritic cells have been discovered with even more specific functions . There is now strong evidence that cells of the dendritic family not only control immunity but also regulate responses to self and non-self, thereby avoiding immunopathology. These two complementary functions are critical to ensure the integrity of the organism in an environment full of microbes and foreign antigens. These cells are also important in the intestinal tract for maintaining the immunologic homeostasis. For instance, CD103+ dendritic cells express indoleamine 2,3-dioxygenase that influences T regulatory/T effector cell balance and oral tolerance induction .
B-lymphocytes produce immunoglobulins but also possess antibody-independent functions. They act as antigen-presenting cells and interact with T lymphocytes optimizing cellular immune responses, although some controversies still exist about these B–T-cell interactions .
5.2.3 T Lymphocytes
T lymphocytes are classically categorized as T-cytotoxic CD8+ (Tc), T-helper CD4+ (Th), and regulatory T cells (Treg), including naturally occurring Foxp3+ CD4+ Tregs. Naïve T lymphocytes are sensitized by antigen-presenting cells and the differentiation and activation status depends on multiple conditions including contact between the T-cell receptor (TCR) with MCH molecules, contact between co-stimulatory receptors and an optimal cytokine environment. Tc plays an important role in viral infections and anti-tumor immunity. On activation after contact between the TCR and MCH class I molecules expressing antigens, cytotoxins such as perforin, granzyme, and granulysin are released. Perforin forms pores in the target cell’s plasma membrane allowing granzymes to enter the target cell, which eventually leads to apoptosis. A second way to induce apoptosis is via cell-surface interactions between the Tc and the infected cell through Fas–Fas ligand interactions. Th aid other immune and non-immune cells, such as epithelial cells, in their defensive actions. Several phenotypes have been defined based on cytokine signatures. However, new variants are still discovered and T-cell plasticity is increasingly recognized showing T cells capable of changing their phenotype, for instance, transition of Tregs into Th17 and vice versa has been reported . Traditionally, Th1 and Th2 were recognized as functionally different Th subtypes . Th1 cells (T bet) are generated from naïve T cells under the influence of IL-12, and IFNγ and Th2 (GATA-3) under the influence of IL-4 and IL-5. Recently, a third subset was discovered, named Th17 (RORγt) generated by IL-1, IL-6, TGF-β, and IL-23 . In their effector functions, these Th subsets also differ. Th1 cells release IL-2, IFNγ, and TNFα and increase the phagocytic and killing capacity of normal macrophages helping them to eliminate intracellular organisms (e.g., Toxoplasma gondii, L. monocytogenes, and Aspergillus spp.). IFNγ also induced anti-viral defenses. Th2 release IL-4, IL-5, and IL-13 and are more specifically involved in extracellular parasitic and worm infections as they boost eosinophilic infiltration and activation. In addition, Th2 contributes to effective B-lymphocyte activation and immunoglobulin production. Th17 have largely been implicated in the defense against extracellular pathogens, both bacteria and fungi, residing at the host barriers of skin and mucosa. Th17 cells release IL-17A, IL-17F, IL-21, and IL-22 contributing to chemotaxis of neutrophils and the increased release of antimicrobial proteins from epithelial cells.
6 Altered Defenses in Cancer
6.1 Physiologic Changes in Cancer
Tumors themselves also predispose to infection by local organ dysfunction. In patients with solid tumors, obstruction of natural passages can lead to inadequate drainage of secretory or excretory fluids from nasal sinuses, bronchi, and bile ducts. Furthermore, tissue invasion may create connections between normally sterile spaces and the environment through disruption of epithelial surfaces. Examples include skin ulcerations with cellulitis and deep soft-tissue infections, and invasion of the bowel wall by tumors of the lower gastrointestinal tract, resulting in bacteremia. Localizations in the central nervous system, spinal cord compression, and paraneoplastic neuropathy are associated with an increased risk of infection due to lethargy and, for instance, a diminished ability to cough and swallow, and incomplete emptying of the bladder .
6.2 Dysfunctional Innate Immunity
Chemotherapy and radiotherapy inflict severe damage upon the different components of the immune system. Physiologic barriers are breached, immune cells decreased in number resulting in neutropenia, monocytopenia, and various degrees of lymphopenia, often accompanied by functional impairment, and the production of humoral factors such as antimicrobial peptides is decreased. In the setting of SCT, extensive immunodeficiencies result from myeloablative conditioning and immunosuppression for graft-versus-host disease (GVHD) prophylaxis. The residual components of the immune system, especially those comprising innate immunity, are of the utmost importance in defending patients against infection , although little is known about which components of the innate immune system remain relatively intact. In general, immune cells such as tissue-residing macrophages, APCs, and NK-cells as well as stromal and epithelial cells and humoral factors such as complement remain . Specialized Paneth cells of the small intestine are also spared from  chemotherapy-induced damage, although the impact on their capacity to produce AMPs is not known. Most of these cells are effective by swiftly recognizing bacterial motifs capable of eliciting immune responses.
Although innate immune components aid in the protection of patients treated with chemotherapy, they also contribute to the inflammatory complications related to the resultant damage that consists of oral and gastrointestinal mucositis , SIRS as well as ARDS and, in the HSCT setting, GVHD and immune-mediated pulmonary complications [97, 98]. The common denominator is an uncontrolled inflammatory response resulting from excessive release of pro-inflammatory cytokines. Central in the pathogenesis of most of these inflammatory conditions is the occurrence of conditioning-induced tissue damage and disturbance of the normal host bacterial homeostasis in these tissues. Chemotherapy and radiotherapy initiate an inflammatory cascade by activating nuclear factor-κB , resulting in the production and release of pro-inflammatory cytokines and chemokines (IL-1, IL-6, IL-8, TNFα, IFNγ) by macrophages, IECs, and endothelial cells [99, 100, 101]. This inflammatory response is subsequently aggravated by the loss of barriers facilitating the translocation of microbes or microbial wall components stimulating PRRs [102, 103, 104] finally, resulting in clinical disorders. In GVHD, the alloreactive T-cell responses are initiated and during the effector phase sustained by innate immune responses.
Besides the loss of adequate barrier function, epithelial cells under “stress” change their attitude toward bacteria and label all microbes as a threat resulting in uncontrolled immune responses . Treatment-related factors mentioned earlier also change the microbial composition, overall with an inversion of the ratio of opportunistic pathogens versus commensals. At the same time, microbes sense the immune status and “stress” of the host and change their behavior by up-regulating virulence factors and becoming genuine pathogens .
6.3 Impairment of Granulocyte Function
Most cytotoxic drugs used in the treatment of malignant diseases have a dose-dependent deleterious effect on the proliferation of normal hematopoietic progenitor cells, including those of the myeloid series. After destruction of the mitotic pool by one or more cytotoxic compounds and depletion of the marrow pool reserve, granulocytopenia lasting days or weeks will ensue, particularly in the treatment of hematologic malignancies and following HSCT-conditioning regimens. Likewise, therapeutic radiation may induce a clinically significant granulocytopenia, depending on dose rate, total dose, irradiated area, and field size. Total body irradiation, as used in HSCT procedures, is the most illustrative of the potential deleterious effects of irradiation. However, both chemotherapeutic drugs and irradiation do not only inhibit the proliferating cell pool, they also interfere with nonproliferating cells and their function. In granulocytes, this may result in decreased chemotaxis, diminished phagocytotic capacity, and defective intracellular killing. Glucocorticosteroids seem to enhance granulocytopoiesis and mobilize the marginal as well as marrow pool reserve, but these supposedly positive effects on the granulocytes are counterbalanced by numerous disadvantages. Indeed, these drugs restrain the accumulation of neutrophils at the site of inflammation through impaired migration, probably due to reduced adherent capacity of the granulocytes, and diminished chemotactic activity. Furthermore, they negatively influence phagocytosis and intracellular killing by neutrophils in a dose-dependent fashion and are associated with a reduction in the number of eosinophils in the blood. Finally, many other drugs, including antibiotics, that are regularly used in cancer patients are known to interfere with the production and function of granulocytes, which also may lead to an increased susceptibility to infection.
Although they usually occur simultaneously, any substantial reduction in the number of granulocytes or qualitative defect in the phagocytic process can, in fact, make the patient prone to recurrent bacterial and fungal infections. It has been shown that an inverse correlation exists between the number of circulating neutrophils and lymphocytes, and the frequency of infection. Depending on the duration of neutropenia, the risk of a febrile episode varies between 30 and 80 %. In a study by Bodey et al. , all patients with a neutrophil count of less than 100/μL for more than 3 weeks developed an infectious complication, and the risk for secondary infections increased proportionally with the duration of granulocytopenia. Moreover, infection-related mortality increased with the duration of hospitalization and the number of days of granulocytopenia.
It may be difficult to establish an unequivocal diagnosis of infection because the inflammatory response in patients without properly functioning granulocytes is muted, thereby obscuring the classic signs and symptoms of infection . Of the episodes of fever associated with granulocytopenia, a definite microbiologic etiology can be established in about a quarter of cases. Local infections, if detected at all, are frequently complicated by bacteremia, which accounts for more than 90 % of culture-documented infections in cancer patients [119, 120].
After bacteria, fungi are the next most common pathogens, especially in immunosuppressed patients who have prolonged and profound granulocytopenia. Autopsy evidence of significant fungal infections can be found in one half of these patients. Most of these infections are not diagnosed or treated antemortem, but they account for 20–30 % of fatal infections in patients with acute leukemia [121, 122, 123]. Besides granulocytopenia, the use of pharmacologic doses of corticosteroids and indwelling catheters may also foster the development of systemic fungal infection .
6.4 Dysfunctional Acquired Immunity
6.4.1 Impaired Humoral Immunity
Humoral immunity is impaired in patients with malignancies, leading to decreased production of immunoglobulins, such as in chronic lymphocytic leukemia (CLL), multiple myeloma, and other lymphoproliferative disorders. Humoral immunity is generally well preserved in patients with acute lymphocytic or myelogenous leukemia. However, with intensive chemotherapy and/or progression of the disease, the capacity to produce immunoglobulins decreases. This may lead to defective opsonization of bacteria and subsequent impairment of phagocytosis by neutrophils and macrophages, adding to the quantitative effect of chemotherapy-induced neutropenia.
Although the humoral response in patients with malignant lymphomas is unimpaired, subsequent radiotherapy and chemotherapy, particularly if both treatment modalities are combined, lead to reduced antibody titers and increased susceptibility to infections with pneumococci and H. influenzae. Splenectomy potentiates the reduction in immunoglobulins by chemotherapy in these patients. Therefore, combined therapy may increase the risk of post-splenectomy bacteremia in patients with lymphoma, and even after curing Hodgkin’s disease, patients are left with a potentially life-threatening humoral immunodeficiency, due to the effects of treatment rather than to the underlying disease itself.
Thus, the advent of more aggressive chemotherapy has changed the classic concept of specific defects of host defense mechanisms in the various types of leukemia and lymphoma. The effects of chemotherapy and radiation are now the primary factor determining the nature and depth of the defect in host defense. Likewise, the increased susceptibility to pneumococci and H. influenzae in patients with CLL or multiple myeloma may be replaced by a defect in cellular immunity and neutrophil function when these patients are being treated with glucocorticosteroids or other agents. Whether patients with hypogammaglobulinemia due to CLL should routinely receive intravenous immunoglobulins has been a matter of considerable debate. A cost-effectiveness analysis has suggested that indiscriminate replacement may not improve quality or length of life in this patient group, and that it is extraordinarily expensive . However, such a decision analysis model cannot be applied to the individual patient who actually has suffered from recurrent bacterial infections. Therefore, it seems reasonable to institute immunoglobulin replacement in those patients who have had a documented infection with pneumococcus or H. influenzae and have decreased serum IgG concentrations.
6.4.2 Impaired Cellular Immunity
The importance of cell-mediated immunity in protecting the host against various intra- and extracellular pathogens is evident from the opportunistic infections occurring in various groups of patients with cancer. Those treated with prednisone or other immunosuppressive agents that affect specific cellular immune responses may be unable to cope with pathogens such as L. monocytogenes, T. gondii, herpesviruses, and fungi. The introduction of monoclonal antibodies including rituximab and alemtuzumab to treat hematologic malignancies has resulted in an increase in opportunistic infections due to the induction of lymphopenia, impaired T lymphocyte responses, and phagocyte dysfunction.
Stem cell transplantation (SCT) results in long-lasting dysfunction of T, B, and NK cells hence opportunistic infections may only become manifest long after transplantation and recovery from neutropenia. The most prominent example is VZV infection, which occurred in up to 50 % of SCT recipients in earlier series, but now significantly less because of the use of prophylaxis with acyclovir during the first year after transplant. Additional viral threats include CMV and EBV reactivation and disease as well as infections due to respiratory viruses. Other opportunistic infections consist of fungal infections as invasive aspergillosis, systemic candidiasis, and Pneumocystis jirovecii infections. The occurrence of these infections after SCT is even more pronounced when acute and chronic GVHD occur as these conditions result in organ damage and require prolonged use of immunosuppressants.
Lymphoproliferative diseases, including Hodgkin’s lymphoma, T-cell non-Hodgkin lymphoma, and CLL themselves can also elicit impaired cellular immune responses. Hodgkin’s lymphoma is a disease that is associated with impaired cellular immunity, although delayed hypersensitivity responses are intact in the majority of untreated patients . The particular defect in T-cell-mediated immunity is probably due to an excess of T-suppressor cells. CLL has also been associated with opportunistic infections, due to a varying degree of defective T-lymphocyte responses, but these defects are most pronounced with an increased duration of the disease and the number of therapies received to treat CLL .
6.5 Mucosal Barrier Injury
The pathobiology of cytotoxic therapy-induced mucositis has been depicted as consisting of five phases that are not necessarily sequential . First, there is an initiation phase in which free radicals are generated and apoptotic cell death is induced by damage to DNA and other structures. Next, the master transcription factor, NF-κB, is involved in the production of the pro-inflammatory cytokines, TNF-α IL-1 and IL-6, which is followed by the amplification and signaling phase of these pro-inflammatory cytokines. Then, there is ulceration, crypt hypoplasia, villous atrophy, and cleavage of extracellular-matrix substrates such as collagen and fibronectin by activated matrix metalloproteinases. This is the phase when bacteria and their cell wall products such as peptidoglycan and lipopolysaccharide are thought to breach the impaired physical barrier more easily and activate tissue macrophages to produce more pro-inflammatory cytokines. The last phase is the healing phase when various factors down-regulate inflammation and restore the integrity of the mucosal barrier. The paracrine mediator of mesenchymal–epithelial communication, keratinocyte growth factor, plays a key role in maintaining the barrier function of epithelial tissues and the healing process after injury .
6.5.1 Effect of Chemotherapy and Irradiation on the Oral Cavity
Because myeloablative regimens deplete the pool of myeloid cells, the patient becomes further dependent on the vestiges of the innate immune system and especially epithelial cells of the digestive tract and skin for protection against potentially lethal infectious complications. These epithelia form an anatomic and immunologic barrier often referred to as the integument that serves as the front line against microbial invasion. Although these epithelia are highly organized and sophisticated structures, the barrier they create is not invincible to microorganisms especially after it is damaged by anti-cancer therapy.
6.5.2 Oral Mucositis
Mucositis is essentially the clinical manifestation of mucosal barrier injury and is characterized by functional complaints such as dysphagia and odynophagia, anatomic changes such as edema, erythema, ulceration, pseudomembrane formation, and alterations in mucus consistency with changes in saliva production (xerostomia). Mucositis results in significant morbidity and markedly lowers the quality of life for several weeks following cytotoxic chemotherapy and irradiation. Modern remission-induction cytostatic chemotherapy and conditioning regimens for HSCT often induce substantial injury to the mucosa. Combinations containing melphalan, etoposide, methotrexate, cytarabine, and idarubicin have all been shown to induce mucositis [134, 135]. Mucositis can be particularly severe when anthracyclines are combined with total body irradiation and cyclophosphamide to condition patients for an allogeneic HSCT . The duration and incidence of fever, parenteral narcotic use, total parenteral nutrition, antibiotic therapy, and the length of stay in a hospital are all correlated with the severity of mucositis, as is the risk of significant infections and mortality [134, 137, 138]. Oral viridans streptococcal infections are related to mucosal barrier injury of the upper part of the digestive tract, particularly the oral cavity, whereas enteric gram-negative bacillary infections and neutropenic enterocolitis are related to the lower part of the digestive tract.
Extensive mucosal damage is often accompanied by a decline in saliva production leading to a dry mouth. Any mucus produced may be extremely viscous and difficult to either swallow or cough up [136, 139]. Periodontal disease may be exacerbated, and minor oral cuts and abrasions may become inflamed and ulcerated. The nonkeratinized surfaces of the mouth, including the underside of the tongue, the roof of the mouth, and the cheeks, may become red, inflamed, and swollen, and thus limit the intake of both food and drink with the risk of malnutrition and catabolism . Moreover, mucosal changes normally progress to a peak severity coinciding independently with the nadir of bone marrow aplasia, and then begin to recover as hematopoiesis returns [130, 140, 141].
Exposing oral commensal flora to the antimicrobial agents used for prophylaxis and local antisepsis will inevitably select for more resistant species. Very susceptible bacteria, such as the oral Neisseria spp., will be suppressed by a wide range of antimicrobials. Others that are marginally susceptible to frequently used agents such as co-trimoxazole, penicillin, and fluoroquinolones, will thrive. This partly explains why the viridans streptococci have become one of the most frequent causes of bacteremia in neutropenic patients who have undergone myelosuppressive chemotherapy or HSCT , although the chemotherapeutic agents may be a more important factor, especially when it induces severe mucosal damage . S. mitis, many of which are actually S. oralis (formerly S. sanguis II) , is causing concern because its appearance in the bloodstream following treatment with high-dose cytarabine is associated with sepsis syndrome and the adult respiratory distress syndrome (ARDS).
Bacteremia due to other unusual oral commensals, such as Stomatococcus, Rothia mucilaginosa, Capnocytophaga spp., and Leptotrichia buccalis, are likely to be selected by quinolone use. In addition, gingivitis as the source of S. epidermidis bacteremia has been reported . Similar risk factors are associated with bacteremia due to members of the S. milleri group . The chlorhexidine mouthwashes used to minimize infective complications arising from the oral toxicity induced by chemotherapy also influence the microflora [133, 147, 148]. The oral flora may also change as a direct result of chemotherapy , and it is likely that more intensive conditioning regimens will aggravate mucositis, leading to a commensurate increase in the number of unusual bacteria.
6.5.3 Gut Mucositis
Besides damage to the oropharyngeal, esophageal, and gastric mucosa, chemotherapy and irradiation impair gut function and lead to rapid alterations in permeability. The increased absorption of sugars such as rhamnose, mannose, and lactulose and the decreased uptake of xylose after chemotherapy, irradiation, or a combination of both indicate a loss of integrity and damage to tight junctions [135, 153, 154]. Impaired gut function and integrity may also facilitate translocation, and blood stream infections of patients colonized with bacteria and fungi . Gut toxicity has also been shown to be responsible for the reduced absorption of quinolones [156, 157] and has been implicated in the erratic bioavailability of the antifungal agent itraconazole and posaconazole [158, 159]. A dysfunctional gut will also have a marked effect on the nutritional status of the patient not least by the diminished release of citrulline by the lower number of functioning enterocytes . This amino acid can be detected in blood and used to determine the extent of gut injury in stem cell transplant recipients .
The gastrointestinal tract has long been implicated as the principal origin of infections caused by the enteric gram-negative bacilli, including E. coli, K. pneumoniae, and Enterobacter spp. , providing the motivation for adopting prophylaxis with fluoroquinolones [162, 163, 164]. More recently, the role of neutropenic enterocolitis or typhlitis, a severe form of mucosal damage of the gut induced by cytotoxic therapy, has also become clearer in providing a portal of entry for various toxin-producing bacteria, including S. aureus, P. aeruginosa, various Clostridium spp. and even Bacillus cereus [165, 166, 167, 168]. This illustrates how the delicate balance between the host and the resident microflora can be disturbed in the setting of mucosal barrier injury and prolonged exposure to antibiotics. Colonization by Candida species of the mucosal surfaces appears to be a prerequisite for local mucosal infection and subsequent invasive disease . Mucosal barrier injury, including neutropenic enterocolitis, is also an independent risk factor for invasive candidiasis among patients receiving cytotoxic chemotherapy [135, 153].
Some chemotherapeutic agents have been shown to have antibacterial activity and even to enhance the effects of antimicrobial agents [176, 177, 178, 179, 180, 181]. The antifungal, miconazole, is also inhibitory to gram-positive bacteria . Gut motility is reduced during parenteral nutrition due to the low amounts of fiber and reduced microbial biomass, which result in dilute feces. When the gut fails to function normally, the protective “anaerobic wallpaper” may still be intact but will be unusually fragile to the effect of antimicrobial agents. Thus, unless placed in a degree of isolation and supplied with low-microbial content diets, patients will be vulnerable to acquiring other gram-negative bacilli from the environment [21, 22, 23].
6.5.4 Mucosal Barrier Injury and Infection
The systemic inflammatory response as measured by CRP appears directly related to the course and extent of mucosal damage reflected by low-citrulline levels rather than infection per se . Also, the risk of infection is significantly higher during chemotherapy cycles that are complicated by mucositis than during those without mucositis. This has been shown for bacteremia due to oral viridans streptococci mainly S. mitis and S. oralis . Drug-induced achlorhydria and the use of antimicrobial prophylaxis with typically but not exclusively fluoroquinolones also contributes toward the development of bacteremia .
Candida spp. normally reside on the mucosal surfaces of the digestive tract of many adults. Adherence to these surfaces appears to be a prerequisite for local infection and subsequent invasive disease since regular surveillance cultures of hematologic patients have shown that colonization invariably precedes infection . Patients treated for AML with either high-dose cytarabine or an anthracycline have low serum D-xylose levels indicating malabsorption and are at higher risk of developing invasive candidiasis. SCT recipients prepared with regimens composed of TBI and patients treated with remission-induction regimens have an increased risk of developing invasive Candida disease.
It is clear from the foregoing that patients with neoplastic diseases seldom suffer impairment of a single defense mechanism. Rather, the risk of infection is the product of the interplay between the many lines of defense, all of which can be breached simultaneously. Moreover, any attempt to confine the damage inflicted upon the host defenses by protecting only one specific line of defense such as the use of growth factors to stimulate hematopoiesis is likely to offer only limited benefit. What is required is a two-pronged approach involving more selective cancer treatment, to avoid damaging healthy tissue combined with strategies that prevent, or at least ameliorate, any unavoidable toxicity. This requires a holistic approach involving both the laboratory and the clinician in continuing to refine therapeutic regimens that are effective and in designing others to cope with the morbidity associated with impaired host defenses. Both are essential to successfully achieve remission of neoplastic disease and to maintain the best quality of life for the patient.
- 1.Johnson CL, Versalovic J (2012) The human microbiome and its potential importance to pediatrics. Pediatrics 129(5):950–960 (PubMed PMID: 22473366. Pubmed Central PMCID: 3340594)Google Scholar
- 2.Chandra RK (1983) Nutrition, immunity, and infection: present knowledge and future directions. Lancet 1(8326 Pt 1):688–691 (PubMed PMID: 6132048. Epub 1983/03/26, Eng)Google Scholar
- 4.Salimonu LS, Ojo-Amaize E, Williams AI, Johnson AO, Cooke AR, Adekunle FA, et al (1982) Depressed natural killer cell activity in children with protein-calorie malnutrition. Clin Immunol Immunopathol 24(1):1–7 (PubMed PMID: 6179671. Epub 1982/07/01, Eng)Google Scholar
- 5.Sugarman B (1983) Zinc and infection. Rev Infect. Dis 5(1):137–147 (PubMed PMID: 6338570. Epub 1983/01/01, Eng)Google Scholar
- 6.Miceli MH, Dong L, Grazziutti ML, Fassas A, Thertulien R, Van Rhee F, et al (2006) Iron overload is a major risk factor for severe infection after autologous stem cell transplantation: a study of 367 myeloma patients. Bone Marrow Transplant 7(9):857–864 (PubMed PMID: 16532017. Eng)Google Scholar
- 7.Craddock PR, Yawata Y, VanSanten L, Gilberstadt S, Silvis S, Jacob HS (1974) Acquired phagocyte dysfunction. A complication of the hypophosphatemia of parenteral hyperalimentation. N Engl J Med 290(25):1403–1407 (PubMed PMID: 4208370. Epub 1974/06/20. Eng)Google Scholar
- 8.McGeer A, Feld R (1994) Epidemiology of infection in immunocompromised oncological patients. Baillikre’s Clin Infect Dis 1:415–438Google Scholar
- 9.Allen J (1981) The diabetic as a compromised host. In: Allen J (ed) Infection and the compromised host: clinical correlations and therapeutic approaches. Williams&Wilkins, Baltimore, pp 229–270Google Scholar
- 10.Rubin J, Yu VL (1988) Malignant external otitis: insights into pathogenesis, clinical manifestations, diagnosis, and therapy. Am J Med 85(3):391–398 (PubMed PMID: 3046354. Epub 1988/09/01. Eng)Google Scholar
- 11.Chayakulkeeree M, Ghannoum MA, Perfect JR (2006) Zygomycosis: the re-emerging fungal infection. Eur J Clin Microbiol Infect Dis 25(4):215–229 (PubMed PMID: 16568297. Eng)Google Scholar
- 12.Cech P, Stalder H, Widmann JJ, Rohner A, Miescher PA (1979) Leukocyte myeloperoxidase deficiency and diabetes mellitus associated with Candida albicans liver abscess. Am J Med 66(1):149–153 (PubMed PMID: 217268. Epub 1979/01/01. Eng)Google Scholar
- 13.Swartz MN (1991) Stress and the common cold. N Engl J Med 325(9):654–656 (PubMed PMID: 1861700. Epub 1991/08/29. Eng)Google Scholar
- 14.Saltzman RL, Peterson PK (1987) Immunodeficiency of the elderly. Rev Infect Dis 9(6):1127–1139 (PubMed PMID: 3321363. Epub 1987/11/01. Eng)Google Scholar
- 17.Schittek B, Hipfel R, Sauer B, Bauer J, Kalbacher H, Stevanovic S, et al (2001) Dermcidin: a novel human antibiotic peptide secreted by sweat glands. Nat Immunol 2(12):1133–1137 (PubMed PMID: 11694882. Epub 2001/11/06. Eng)Google Scholar
- 22.Van Der Waaij D (1979) The colonization resistance of the digestive tract of man and animals. Gustav Fischer Verlag, New YorkGoogle Scholar
- 23.Young LS (1988) Antimicrobial prophylaxis in the neutropenic host: lessons of the past and perspectives for the future. Eur J Clin Microbiol Infect Dis 1988 7(1):93–97 (PubMed PMID: 3132393. Epub 1988/02/01. Eng)Google Scholar
- 26.Van der Waaij D (1984) Effect of antibiotics on colonization resistance. In: Easmon CS (ed) Medical microbiology, 4th edn. Academic Press Inc, London, pp 227–237Google Scholar
- 28.Meijer-Severs GJ, van Santen E (1987) Short-chain fatty acids and succinate in feces of healthy human volunteers and their correlation with anaerobe cultural counts. Scand J Gastroenterol 22(6):672–676 (PubMed PMID: 3659829. Epub 1987/08/01. Eng)Google Scholar
- 32.Pizzo PA, Robichaud KJ, Edwards BK, Schumaker C, Kramer BS, Johnson A (1983) Oral antibiotic prophylaxis in patients with cancer: a double-blind randomized placebo-controlled trial. J Pediatr 102(1):125–133 (PubMed PMID: 6336781. Epub 1983/01/01. Eng)Google Scholar
- 33.Walsh TJ, Schimpff SC (1983) Prevention of infection among patients with cancer. Eur J Cancer Clin Oncol 19(10):1333–1344 (PubMed PMID: 6416846. Epub 1983/10/01. Eng)Google Scholar
- 41.Clasener HA, Vollaard EJ, van Saene HK (1987) Long-term prophylaxis of infection by selective decontamination in leukopenia and in mechanical ventilation. Rev Infect Dis 9(2):295–328 (PubMed PMID: 3296099. Epub 1987/03/01. Eng)Google Scholar
- 42.Van der Leur JJ, Thunnissen PL, Clasener HA, Muller NF, Dofferhoff AS (1993) Effects of imipenem, cefotaxime and cotrimoxazole on aerobic microbial colonization of the digestive tract. Scand J Infect Dis 25(4):473–478 (PubMed PMID: 8248747. Epub 1993/01/01. Eng)Google Scholar
- 48.Chomarat M, Espinouse D (1991) Lactobacillus rhamnosus septicemia in patients with prolonged aplasia receiving ceftazidime-vancomycin. Eur J Clin Microbiol Infect Dis 10(1):44 (PubMed PMID: 2009881. Epub 1991/01/01. Eng)Google Scholar
- 51.Kern WV, Andriof E, Oethinger M, Kern P, Hacker J, Marre R (1994) Emergence of fluoroquinolone-resistant Escherichia coli at a cancer center. Antimicrob Agents Chemother 38(4):681–687 (PubMed PMID: 8031031. Pubmed Central PMCID: 284525. Epub 1994/04/01. Eng)Google Scholar
- 53.Iwasaki A, Medzhitov R (2004) Toll-like receptor control of the adaptive immune responses. Nat Immunol 5(10):987–995 (PubMed PMID: 15454922. Epub 2004/09/30. Eng)Google Scholar
- 54.Medzhitov R, Janeway CA Jr (1998) Innate immune recognition and control of adaptive immune responses. Semin Immunol 10(5):351–353 (PubMed PMID: 9799709. Epub 1998/11/04. Eng)Google Scholar
- 55.Medzhitov R, Janeway C Jr (2000) Innate immunity. N Engl J Med 343(5):338–344 (PubMed PMID: 10922424. Epub 2000/08/03. Eng)Google Scholar
- 56.Pitman RS, Blumberg RS (2000) First line of defense: the role of the intestinal epithelium as an active component of the mucosal immune system. J Gastroenterol 35(11):805–814 (PubMed PMID: 11085489. Epub 2000/11/21. Eng)Google Scholar
- 57.Akira S, Uematsu S, Takeuchi O (2006) Pathogen recognition and innate immunity. Cell 124(4):783–801 (PubMed PMID: 16497588. Epub 2006/02/25. Eng)Google Scholar
- 58.Robinson MJ, Sancho D, Slack EC, LeibundGut-Landmann S, Reis e Sousa C (2006) Myeloid C-type lectins in innate immunity. Nat Immunol 7(12):1258–1265 (PubMed PMID: 17110942. Epub 2006/11/18. Eng)Google Scholar
- 59.Strober W, Murray PJ, Kitani A, Watanabe T (2006) Signalling pathways and molecular interactions of NOD1 and NOD2. Nat Rev Immunol 6(1):9–20 (PubMed PMID: 16493424. Epub 2006/02/24. Eng)Google Scholar
- 60.Bianchi ME (2007) DAMPs, PAMPs and alarmins: all we need to know about danger. J Leukoc Biol 81(1):1–5 (PubMed PMID: 17032697. Epub 2006/10/13. Eng)Google Scholar
- 61.Medzhitov R, Janeway CA Jr (2002) Decoding the patterns of self and nonself by the innate immune system. Science 296(5566):298–300 (PubMed PMID: 11951031. Epub 2002/04/16. Eng)Google Scholar
- 62.Matzinger P (2002) The danger model: a renewed sense of self. Science 296(5566):301–305 (PubMed PMID: 11951032. Epub 2002/04/16. Eng)Google Scholar
- 63.Barton GM (2008) A calculated response: control of inflammation by the innate immune system. J Clin Invest 118(2):413–420 (PubMed PMID: 18246191. Pubmed Central PMCID: 2214713. Epub 2008/02/05. Eng)Google Scholar
- 64.Underhill DM (2003) Toll-like receptors: networking for success. Eur J Immunol 33(7):1767–1775 (PubMed PMID: 12811836. Epub 2003/06/18. Eng)Google Scholar
- 65.Han J, Ulevitch RJ (2005) Limiting inflammatory responses during activation of innate immunity. Nat Immunol 6(12):1198–1205 (PubMed PMID: 16369559. Epub 2005/12/22. Eng)Google Scholar
- 66.Mookherjee N, Hancock RE (20007) Cationic host defence peptides: innate immune regulatory peptides as a novel approach for treating infections. Cell Mol Life Sci 64(7–8):922–933 (PubMed PMID: 17310278. Epub 2007/02/21. Eng)Google Scholar
- 67.Scott MG, Hancock RE (2000) Cationic antimicrobial peptides and their multifunctional role in the immune system. Crit Rev Immunol 20(5):407–431 (PubMed PMID: 11145218. Epub 2001/01/06. Eng)Google Scholar
- 68.Zasloff M (2002) Antimicrobial peptides of multicellular organisms. Nature 415(6870):389–395 (PubMed PMID: 11807545. Epub 2002/01/25. Eng)Google Scholar
- 69.Ware AJ, Coller BS (1995) Platelet morphology, biochemistry, and function. In: Beutler E, Lichtman MA, Coller BS, Kipps TJ (eds) Williams hematology. McGraw-Hill, New York, pp 1161–1201Google Scholar
- 70.Viscoli C, Bruzzi P, Castagnola E, Boni L, Calandra T, Gaya H, et al (1994) Factors associated with bacteraemia in febrile, granulocytopenic cancer patients. The International Antimicrobial Therapy Cooperative Group (IATCG) of the European Organization for Research and Treatment of Cancer (EORTC). Eur J Cancer 30A(4):430–437 (PubMed PMID: 8018397. Eng)Google Scholar
- 71.Cronkite EP, Fliedner TM (1964) Granulocytopoiesis. N Engl J Med 270:1347–1352 CONTD (PubMed PMID: 14140268. Epub 1964/06/18. Eng)Google Scholar
- 73.Weller PF (1991) The immunobiology of eosinophils. N Engl J Med 324(16):1110–1118 (PubMed PMID: 2008184. Epub 1991/04/18. Eng)Google Scholar
- 74.Lanier LL (2008) Up on the tightrope: natural killer cell activation and inhibition. Nat Immunol 9(5):495–502 (PubMed PMID: 18425106. Pubmed Central PMCID: 2669298)Google Scholar
- 76.Artis D (2008) Epithelial-cell recognition of commensal bacteria and maintenance of immune homeostasis in the gut. Nat Rev Immunol 8(6):411–420 (PubMed PMID: 18469830. Epub 2008/05/13. Eng)Google Scholar
- 77.Backhed F, Ley RE, Sonnenburg JL, Peterson DA, Gordon JI (2005) Host-bacterial mutualism in the human intestine. Science 307(5717):1915–1920 (PubMed PMID: 15790844. Epub 2005/03/26. Eng)Google Scholar
- 78.Rescigno M, Lopatin U, Chieppa M (2008) Interactions among dendritic cells, macrophages, and epithelial cells in the gut: implications for immune tolerance. Curr Opin Immunol 20(6):669–675 (PubMed PMID: 18852045. Epub 2008/10/15. Eng)Google Scholar
- 79.Rimoldi M, Chieppa M, Salucci V, Avogadri F, Sonzogni A, Sampietro GM, et al (2005) Intestinal immune homeostasis is regulated by the crosstalk between epithelial cells and dendritic cells. Nat Immunol 6(5):507–514 (PubMed PMID: 15821737. Epub 2005/04/12. Eng)Google Scholar
- 80.Cario E (2008) Barrier-protective function of intestinal epithelial Toll-like receptor 2. Mucosal Immunol 1(1):S62–S66 (PubMed PMID: 19079234. Epub 2008/12/23. Eng)Google Scholar
- 81.Lee J, Mo JH, Katakura K, Alkalay I, Rucker AN, Liu YT, et al. Maintenance of colonic homeostasis by distinctive apical TLR9 signalling in intestinal epithelial cells. Nat Cell Biol 8(12):1327–1336 (PubMed PMID: 17128265. Epub 2006/11/28. Eng)Google Scholar
- 82.Rakoff-Nahoum S, Paglino J, Eslami-Varzaneh F, Edberg S, Medzhitov R (2004) Recognition of commensal microflora by toll-like receptors is required for intestinal homeostasis. Cell 118(2):229–241 (PubMed PMID: 15260992. Epub 2004/07/21. Eng)Google Scholar
- 83.McGuckin MA, Eri R, Simms LA, Florin TH, Radford-Smith G (2009) Intestinal barrier dysfunction in inflammatory bowel diseases. Inflamm Bowel Dis 15(1):100–113 (PubMed PMID: 18623167. Epub 2008/07/16. Eng)Google Scholar
- 84.McInturff JE, Modlin RL, Kim J. The role of toll-like receptors in the pathogenesis and treatment of dermatological disease (2005) J Invest Dermatol 125(1):1–8 (PubMed PMID: 15982296. Epub 2005/06/29. Eng)Google Scholar
- 85.Rogler G (2004) Update in inflammatory bowel disease pathogenesis. Curr Opin Gastroenterol 20(4):311–317 (PubMed PMID: 15703658. Epub 2005/02/11. Eng)Google Scholar
- 86.Sansonetti PJ (2008) Host-bacteria homeostasis in the healthy and inflamed gut. Curr Opin Gastroenterol 24(4):435–439 (PubMed PMID: 18622156. Epub 2008/07/16. Eng)Google Scholar
- 89.Lund FE, Randall TD (2010) Effector and regulatory B cells: modulators of CD4(+) T cell immunity. Nat Rev Immunol 10(4):236–247 (PubMed PMID: 20224569. Pubmed Central PMCID: 3038334)Google Scholar
- 93.Neth OW, Bajaj-Elliott M, Turner MW, Klein NJ (2005) Susceptibility to infection in patients with neutropenia: the role of the innate immune system. Br J Haematol 129(6):713–722 (PubMed PMID: 15952996. Epub 2005/06/15. Eng)Google Scholar
- 94.Geddes M, Storek J (2007) Immune reconstitution following hematopoietic stem-cell transplantation. Best Pract Res Clin Haematol 20(2):329–348 (PubMed PMID: 17448965. Epub 2007/04/24. Eng)Google Scholar
- 95.Verburg M, Renes IB, Meijer HP, Taminiau JA, Buller HA, Einerhand AW, et al (2000) Selective sparing of goblet cells and paneth cells in the intestine of methotrexate-treated rats. Am J Physiol Gastrointest Liver Physiol 2000 279(5):G1037–G1047 (PubMed PMID: 11053002. Epub 2000/10/29. Eng)Google Scholar
- 96.Blijlevens NM, Donnelly JP, DePauw BE (2005) Inflammatory response to mucosal barrier injury after myeloablative therapy in allogeneic stem cell transplant recipients. Bone Marrow Transplant 36(8):703–707 (PubMed PMID: 16062174. Epub 2005/08/03. Eng)Google Scholar
- 97.Cooke KR (2005) Acute lung injury after allogeneic stem cell transplantation: from the clinic, to the bench and back again. Pediatr Transplant 9(7):25–36 (PubMed PMID: 16305615. Epub 2005/11/25. Eng)Google Scholar
- 98.Ferrara JL, Levine JE, Reddy P, Holler E. Graft-versus-host disease (2009) Lancet 373(9674):1550–1561 (PubMed PMID: 19282026. Pubmed Central PMCID: 2735047. Epub 2009/03/14. Eng)Google Scholar
- 99.Sonis ST (2002) The biologic role for nuclear factor-kappaB in disease and its potential involvement in mucosal injury associated with anti-neoplastic therapy. Crit Rev Oral Biol Med 13(5):380–389 (PubMed PMID: 12393757. Epub 2002/10/24. Eng)Google Scholar
- 100.Logan RM, Stringer AM, Bowen JM, Yeoh AS, Gibson RJ, Sonis ST, et al (2007) The role of pro-inflammatory cytokines in cancer treatment-induced alimentary tract mucositis: pathobiology, animal models and cytotoxic drugs. Cancer Treat Rev 33(5):448–460 (PubMed PMID: 17507164. Epub 2007/05/18. Eng)Google Scholar
- 101.Xun CQ, Thompson JS, Jennings CD, Brown SA, Widmer MB (1994) Effect of total body irradiation, busulfan-cyclophosphamide, or cyclophosphamide conditioning on inflammatory cytokine release and development of acute and chronic graft-versus-host disease in H-2-incompatible transplanted SCID mice. Blood 83(8):2360–2367 (PubMed PMID: 8161803. Epub 1994/04/15. Eng)Google Scholar
- 102.Levy O, Teixeira-Pinto A, White ML, Carroll SF, Lehmann L, Wypij D, et al (2003) Endotoxemia and elevation of lipopolysaccharide-binding protein after hematopoietic stem cell transplantation. Pediatr Infect Dis J 22(11):978–981 (PubMed PMID: 14614371. Epub 2003/11/14. Eng)Google Scholar
- 103.Song D, Shi B, Xue H, Li Y, Yang X, Yu B, et al (2006) Confirmation and prevention of intestinal barrier dysfunction and bacterial translocation caused by methotrexate. Dig Dis Sci 51(9):1549–1556 (PubMed PMID: 16927144. Epub 2006/08/24. Eng)Google Scholar
- 104.Tsuji E, Hiki N, Nomura S, Fukushima R, Kojima J, Ogawa T, et al (2003) Simultaneous onset of acute inflammatory response, sepsis-like symptoms and intestinal mucosal injury after cancer chemotherapy. Int J Cancer 107(2):303–308 (PubMed PMID: 12949812. Epub 2003/09/02. Eng)Google Scholar
- 105.Nazli A, Yang PC, Jury J, Howe K, Watson JL, Soderholm JD, et al (2004) Epithelia under metabolic stress perceive commensal bacteria as a threat. Am J Pathol 164(3):947–957 (PubMed PMID: 14982848. Pubmed Central PMCID: 1614709. Epub 2004/02/26. Eng)Google Scholar
- 106.Alverdy J, Zaborina O, Wu L (2005) The impact of stress and nutrition on bacterial-host interactions at the intestinal epithelial surface. Curr Opin Clin Nutr Metab Care 8(2):205–209 (PubMed PMID: 15716801. Epub 2005/02/18. Eng)Google Scholar
- 107.Kallianpur AR (2005) Genomic screening and complications of hematopoietic stem cell transplantation: has the time come? Bone Marrow Transplant 35(1):1–16 (PubMed PMID: 15489868. Epub 2004/10/19. Eng)Google Scholar
- 108.Bochud PY, Chien JW, Marr KA, Leisenring WM, Upton A, Janer M, et al (2008) Toll-like receptor 4 polymorphisms and aspergillosis in stem-cell transplantation. N Engl J Med 359(17):1766–1777 (PubMed PMID: 18946062. Pubmed Central PMCID: 2656610. Epub 2008/10/24. Eng)Google Scholar
- 109.Cook M, Briggs D, Craddock C, Mahendra P, Milligan D, Fegan C, et al (2006) Donor KIR genotype has a major influence on the rate of cytomegalovirus reactivation following T-cell replete stem cell transplantation. Blood 107(3):1230–1232 (PubMed PMID: 16239436. Epub 2005/10/22. Eng)Google Scholar
- 110.Mullighan CG, Heatley S, Doherty K, Szabo F, Grigg A, Hughes TP, et al (2002) Mannose-binding lectin gene polymorphisms are associated with major infection following allogeneic hemopoietic stem cell transplantation. Blood 99(10):3524–3529 (PubMed PMID: 11986203. Epub 2002/05/03. Eng)Google Scholar
- 111.Dickinson AM, Holler E (2008) Polymorphisms of cytokine and innate immunity genes and GVHD. Best Pract Res Clin Haematol 21(2):149–164 (PubMed PMID: 18503983. Epub 2008/05/28. Eng)Google Scholar
- 112.Mullally A, Ritz J (2007) Beyond HLA: the significance of genomic variation for allogeneic hematopoietic stem cell transplantation. Blood 109(4):1355–1362 (PubMed PMID: 17008540. Epub 2006/09/30. Eng)Google Scholar
- 113.Hildebrandt GC, Granell M, Urbano-Ispizua A, Wolff D, Hertenstein B, Greinix HT, et al (2008) Recipient NOD2/CARD15 variants: a novel independent risk factor for the development of bronchiolitis obliterans after allogeneic stem cell transplantation. Biol Blood Marrow Transplant 14(1):67–74 (PubMed PMID: 18158963. Epub 2007/12/27. Eng)Google Scholar
- 114.Holler E, Rogler G, Herfarth H, Brenmoehl J, Wild PJ, Hahn J, et al (2004) Both donor and recipient NOD2/CARD15 mutations associate with transplant-related mortality and GvHD following allogeneic stem cell transplantation. Blood 104(3):889–894 (PubMed PMID: 15090455. Epub 2004/04/20. Eng)Google Scholar
- 115.Kanzler H, Barrat FJ, Hessel EM, Coffman RL (2007) Therapeutic targeting of innate immunity with Toll-like receptor agonists and antagonists. Nat Med 13(5):552–529 (PubMed PMID: 17479101. Epub 2007/05/05. Eng)Google Scholar
- 116.O’Neill LA (2003) Therapeutic targeting of Toll-like receptors for inflammatory and infectious diseases. Curr Opin Pharmacol 3(4):396–403 (PubMed PMID: 12901949. Epub 2003/08/07. Eng)Google Scholar
- 126.Young RC, Corder MP, Haynes HA, DeVita VT (1972) Delayed hypersensitivity in Hodgkin’s disease. A study of 103 untreated patients. Am J Med 52(1):63–72 (PubMed PMID: 5058359. Epub 1972/01/01. Eng)Google Scholar
- 127.Deardon C (2008) Chronic lymphocytic leukemia. ASH Education, Hematology, pp 450–456Google Scholar
- 128.Sonis ST (2004) The pathobiology of mucositis. Nat Rev 4(4):277–284 (PubMed PMID: 15057287. Eng)Google Scholar
- 129.Blijlevens NM, Logan RM, Netea MG (2009) The changing face of febrile neutropenia—from monotherapy to moulds to mucositis. Mucositis: from febrile neutropenia to febrile mucositis. J Antimicrob Chemother 63(1):i36–i40 (PubMed PMID: 19372181. Epub 2009/04/23. Eng)Google Scholar
- 132.Rocke LK, Loprinzi CL, Lee JK, Kunselman SJ, Iverson RK, Finck G, et al (1993) A randomized clinical trial of two different durations of oral cryotherapy for prevention of 5-fluorouracil-related stomatitis. Cancer 72(7):2234–2238 (PubMed PMID: 8374882. Eng)Google Scholar
- 133.Weisdorf DJ, Bostrom B, Raether D, Mattingly M, Walker P, Pihlstrom B, et al (1989) Oropharyngeal mucositis complicating bone marrow transplantation: prognostic factors and the effect of chlorhexidine mouth rinse. Bone Marrow Transplant 4(1):89–95 (PubMed PMID: 2647192. Eng)Google Scholar
- 134.Blijlevens N, Schwenkglenks M, Bacon P, D’Addio A, Einsele H, Maertens J, et al (2008) Prospective oral mucositis audit: oral mucositis in patients receiving high-dose melphalan or BEAM conditioning chemotherapy—European Blood and Marrow Transplantation Mucositis Advisory Group. J Clin Oncol 26(9):1519–1525 (PubMed PMID: 18268357. Eng)Google Scholar
- 136.Raemaekers J, De Witte T, Schattenberg A, Van der Lely N (1989) Prevention of leukemic relapse after transplantation with lymphocyte depleted marrow by intensification of the conditioning regimen with a 6-day continuous infusion of anthracyclines. Bone Marrow Transplant 4(2):167–171 (PubMed PMID: 2650787. Epub 1989/03/01. Eng)Google Scholar
- 137.Sonis ST, Oster G, Fuchs H, Bellm L, Bradford WZ, Edelsberg J, et al (2001) Oral mucositis and the clinical and economic outcomes of hematopoietic stem-cell transplantation. J Clin Oncol 19(8):2201–2205 (PubMed PMID: 11304772. Eng)Google Scholar
- 138.Fanning SR, Rybicki L, Kalaycio M, Andresen S, Kuczkowski E, Pohlman B, et al (2006) Severe mucositis is associated with reduced survival after autologous stem cell transplantation for lymphoid malignancies. Br J Haematol 135(3):374–381 (PubMed PMID: 16995885. Eng)Google Scholar
- 139.McGuire DB, Altomonte V, Peterson DE, Wingard JR, Jones RJ, Grochow LB (1993) Patterns of mucositis and pain in patients receiving preparative chemotherapy and bone marrow transplantation. Oncol Nurs Forum 20(10):1493–1502 (PubMed PMID: 8278277. Eng)Google Scholar
- 140.Donnelly JP, Maschmeyer G, Daenen S (1992) Selective oral antimicrobial prophylaxis for the prevention of infection in acute leukaemia—ciprofloxacin versus co-trimoxazole plus colistin. The EORTC-Gnotobiotic Project Group. Eur J Cancer 959–8049Google Scholar
- 141.Morrison VA, Haake RJ, Weisdorf DJ (1993) The spectrum of non-Candida fungal infections following bone marrow transplantation. Medicine (Baltimore) 72(2):78–89 (PubMed PMID: 8479326. Epub 1993/03/01. Eng)Google Scholar
- 150.Bronchud M (1993) Can hematopoietic growth factors be used to improve the success of cytotoxic chemotherapy? Anticancer Drugs 4(2):127–139 (PubMed PMID: 8490192. Epub 1993/04/01. Eng)Google Scholar
- 152.De Witte T, Van Der Lely N, Muus P, Donnelly JP, Schattenberg T (1993) Recombinant human granulocyte macrophage colony stimulating factor (rhGM-CSF) accelerates bone marrow recovery after allogeneic T-cell depleted bone marrow transplantation. L’Ospedale Maggiore 87(1):42–46Google Scholar
- 159.Gubbins PO, Krishna G, Sansone-Parsons A, Penzak SR, Dong L, Martinho M, et al (2006) Pharmacokinetics and safety of oral posaconazole in neutropenic stem cell transplant recipients. Antimicrob Agents Chemother 50(6):1993–1999 (PubMed PMID: 16723557. Eng)Google Scholar
- 160.Blijlevens NM, Lutgens LC, Schattenberg AV, Donnelly JP (2004) Citrulline: a potentially simple quantitative marker of intestinal epithelial damage following myeloablative therapy. Bone Marrow Transplant 34(3):193–196 (PubMed PMID: 15170165. Eng)Google Scholar
- 163.Engels EA, Lau J, Barza M (1998) Efficacy of quinolone prophylaxis in neutropenic cancer patients: a meta-analysis. J Clin Oncol 16(3):1179–1187 (PubMed PMID: 9508206. Eng)Google Scholar
- 164.Gafter-Gvili A, Paul M, Fraser A, Leibovici L (2007) Effect of quinolone prophylaxis in afebrile neutropenic patients on microbial resistance: systematic review and meta-analysis. J Antimicrob Chemother 59(1):5–22 (PubMed PMID: 17077101. Eng)Google Scholar
- 165.Coleman N, Speirs G, Khan J, Broadbent V, Wight DG, Warren RE (1993) Neutropenic enterocolitis associated with Clostridium tertium. J Clin Pathol 46(2):180–183 (PubMed PMID: 8459041. Eng)Google Scholar
- 166.Gomez L, Martino R, Rolston KV (1998) Neutropenic enterocolitis: spectrum of the disease and comparison of definite and possible cases. Clin Infect Dis 27(4):695–699 (PubMed PMID: 9798018. Eng)Google Scholar
- 168.Ginsburg AS, Salazar LG, True LD, Disis ML (2003) Fatal Bacillus cereus sepsis following resolving neutropenic enterocolitis during the treatment of acute leukemia. Am J Hematol 72(3):204–208 (PubMed PMID: 12605393. Eng)Google Scholar
- 169.Nucci M, Anaissie E (2001) Revisiting the source of candidemia: skin or gut? Clin Infect Dis 33(12):1959–1967 (PubMed PMID: 11702290. Eng)Google Scholar
- 172.Callum JL, Brandwein JM, Sutcliffe SB, Scott JG, Keating A (1991) Influence of total body irradiation on infections after autologous bone marrow transplantation. Bone Marrow Transplant 8(4):245–251 (PubMed PMID: 1756321. Epub 1991/10/01. Eng)Google Scholar
- 173.Johnson S, Driks MR, Tweten RK, Ballard J, Stevens DL, Anderson DJ, et al (1994) Clinical courses of seven survivors of Clostridium septicum infection and their immunologic responses to alpha toxin. Clin Infect Dis 19(4):761–764 (PubMed PMID: 7803645. Epub 1994/10/01. Eng)Google Scholar
- 174.Blijlevens NM, Donnelly JP, De Pauw BE (2000) Mucosal barrier injury: biology, pathology, clinical counterparts and consequences of intensive treatment for haematological malignancy: an overview. Bone Marrow Transplant 25(12):1269–1278 (PubMed PMID: 10871732. Eng)Google Scholar
- 176.Bergström P, Grankvist K, Henriksson R (1994) Interaction between antibiotics and antineoplastic drugs on antibacterial activity in vitro: estramustine phosphate sensitizes pneumococci to amikacin. Int J Oncol 4:43–439Google Scholar
- 180.Neuman M (1992) The antimicrobial activity of non-antibiotics—interactions with antibiotics. APMIS 100(30):15–23Google Scholar
- 181.Bodet CA 3rd, Jorgensen JH, Drutz DJ (1985) Antibacterial activities of antineoplastic agents. Antimicrob Agents Chemother 28(3):437–439 (PubMed PMID: 2416271. Pubmed Central PMCID: 180269. Epub 1985/09/01. Eng)Google Scholar
- 183.van der Velden WJ, Blijlevens NM, Feuth T, Donnelly JP (2009) Febrile mucositis in haematopoietic SCT recipients. Bone Marrow Transplant 43(1):55–60 (PubMed PMID: 18762766. Epub 2008/09/03. Eng)Google Scholar
- 184.Marron A, Carratala J, Gonzalez-Barca E, Fernandez-Sevilla A, Alcaide F, Gudiol F (2000) Serious complications of bacteremia caused by Viridans streptococci in neutropenic patients with cancer. Clin Infect Dis 31(5):1126–1130 (PubMed PMID: 11073739. Epub 2000/11/14. Eng)Google Scholar