Abstract
Hanseniasis comprises one of the main causes of physical disabilities due to its potential to strike neural lesions, foot deformities, amputations, and mutilations. Since innate response is important in hanseniasis, this work reviewed and updated the role of reactive oxygen/nitrogen species in different clinical forms of hanseniasis, as well as their role in different phagocyte free radicals’ generator systems (NADPH-oxidase, mitochondrial pathways, myeloperoxidase, extracellular traps, iNOS). Since hanseniasis can induce antioxidant depletion, possible benefits of antioxidant nutritional supplementation are also discussed.
This is a preview of subscription content, log in via an institution.
Buying options
Tax calculation will be finalised at checkout
Purchases are for personal use only
Learn about institutional subscriptionsReferences
Slim FJ, Keukenkamp R, van Schie CH, Faber WR, Nollet F (2011) Foot Impairments and limitations in walking activities in people affected by leprosy. J Rehabil Med 43(1):32–38
Nsagha DS, Bissek AZ, Nsagha SM et al (2011) Social stigma as an epidemiological determinant for leprosy elimination in Cameroon. J Public Health Afr 2(1):e10. https://doi.org/10.4081/jphia.2011.e10
Faria L, Santos LAC (2015) A hanseníase e sua história no Brasil: a história de um “flagelo nacional”. Hist Cienc Saude-Manguinhos 22(4):1491–1495
WHO (2016) Global leprosy update, 2016: accelerating reduction of disease burden. Weekly Epidemiol Rec 92(35):501–520
Worldometers (2018) India population. Available at: http://www.worldometers.info/world-population/india-population/ (06/03/2018)
da Saúde M (2018) Secretaria de Vigilância Sanitária. Caracterização da situação epidemiológica da hanseníase e diferenças por sexo, Brasil, 2012–2016. Bol Epidemiol 49(4):1–10
Santos MJS, Ferrari CKB, de Toledo OR, de Moraes EV, David FL (2012) Leprosy among children and adolescents under 15 years-old in a city of Legal Amazon, Brazil. Indian J Leprosy 84:265–269
Fonseca GAA, Silva TC, Ferrari GSL, Ferrari CKB (2013) Epidemiological aspects of leprosy in a city of Legal Amazon, Brazil. Int J Sci Nat 4(4):576–578
Wiedau-Pazos M, Goto JJ, Rabizadeh S et al (1996) Altered reactivity of superoxide dismutase in familial amyotrophic lateral sclerosis. Science 271(5248):515–518
Sandoval M, Zhang X-J, Liu X, Mannick EE, Clark DA, Miller MJS (1997) Peroxynitrite-induced apoptosis in T84 and RAW 264 cells: attenuation by L-ascorbic acid. Free Rad Biol Med 22(3):489–495
Ferrari CKB (2000) Free radicals, lipid peroxidation and antioxidants in apoptosis: implications in cancer, cardiovascular and neurological diseases. Biologia 55(6):581–590
da Silva WJM, Ferrari CKB (2011) Mitochondrial metabolism, free radicals and aging. Rev Bras Geriatr Gerontol 14(3):441–451
Duthie GG (1993) Lipid peroxidation. Eur J Clin Nutr 47(11):759–764
Halliwell B (1994) Free radicals, antioxidants and human disease: curiosity, cause or consequence? Lancet 344(8924):721–724
Ferrari CK, França EL, Honorio-França AC (2009) Nitric oxide, health and disease. J Appl Biomed 7:163–173
Ferrari CKB (1998) Lipid oxidation in food and biological systems: general mechanisms and nutritional and pathological implications. Rev Nutr 11(1):3–14
Ferrari CKB (2001) Oxidative stress pathophysiology: searching for an effective antioxidant protection. Int Med J 8(3):175–184
Suzuki YJ, Carini M, Butterfield DA (2010) Protein carbonylation. Antiox Redox Signal 12(3):323–325
Rimoli LF, Godoy MF (2011) Efetividade da vitamina E sobre o estresse oxidativo, em hansenianos da forma multibacilar sob tratamento. Hansen Int 36(1):17–21
Schalcher TR, Borges RS, Coleman MD et al (2014) Clinical oxidative stress during leprosy multidrug therapy: impact of dapsone oxidation. PLoS One 9(1):e85712. https://doi.org/10.1371/journal.pone.0085712
Babior BM, Cumutte JT, Kipnes RS (1975) Biological defense mechanisms. Evidence for the participation of superoxide in bacterial killing by xanthine oxidase. J Lab Clin Med 85(2):235–244
Babior BM (1984) The respiratory burst of phagocytes. J Clin Invest 73:599–601
Halliwell B, Chirico S (1993) Lipid peroxidation: its mechanism, measurement, and significance. Am J Clin Nutr 57(5):S715–S725
Kanner J (1994) Oxidative processes in meat and meat products: quality implications. Meat Sci 36(1/2):169–189
Esterbauer H (1993) Cytotoxicity and genotoxicity of lipid-oxidation products. Am J Clin Nutr 57(5):S779–S786
Beers RF Jr, Sizër IW (1952) A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J Biol Chem 195:133–140
Lee JN, Dutta RK, Maharjan Y et al (2018) Catalase inhibition induces pexophagy through ROS accumulation. Biochem Biophys Res Commun 501(3):696–702
Ferrari CKB, Souto PCS, França EL, Honorio-França AC (2011) Oxidative and nitrosative stress on phagocytes’ function: from effective defense to immunity evasion mechanisms. Arch Immunol Ther Exp 59(6):441–448
von Köckritz-Blickwede M, Nizet V (2009) Innate immunity turned inside-out: antimicrobial defense by phagocyte extracellular traps. J Mol Med 87:775–783
Ramos-Kichik V, Mondragón-Flores R, Mondragón-Castelán M (2009) Neutrophil extracellular traps are induced by Mycobacterium tuberculosis. Tuberculosis 89:29–37
Palmer RMJ, Ashton DS, Moncada S (1988) Vascular endothelial cells synthesize nitric oxide from arginine. Nature 333:664–666
Ahmad R, Rasheed Z, Ahsan H (2009) Biochemical and cellular toxicology of peroxynitrite: implications in cell death and autoimmune phenomenon. Immunopharmacol Immunotoxicol 31(3):388–396
Khan MA, Alam K, Zafaryab M, Rizvi MA (2017) Peroxynitrite-modified histone as a pathophysiological biomarker in autoimmune diseases. Biochimie 140:1–9
Visca P, Fabozzi G, Milani M, Bolognesi M, Ascenzi P (2002) Nitric oxide and Mycobacterium leprae pathogenicity. IUBMB Life 54(3):95–99
Boga P, Shety VP, Khan Y (2001) Nitric oxide metabolites in sera of patients across the spectrum of leprosy. Indian J Lepr 82(3):123–129
Adams LB, Scollard DM, Ray NA et al (2002) The study of Mycobacterium leprae infection in interferon-gamma gene-disrupted mice as a model to explore the immunopathologic spectrum of leprosy. J Infect Dis 185(Suppl.1):S1–S8
Adams LB, Job CK, Krahenbuhl JL (2000) Role of inducible nitric oxide synthase in resistance to Mycobacterium leprae in mice. Infect Immun 68(9):5462–5465
Vladimirov YA, Proskurnina EV (2009) Free radicals and cell chemiluminescence. Biochemistry 74:1545–1566
Nauseef WM (2014) Myeloperoxidase in human neutrophil host defense. Cell Microbiol 16(8):1146–1155
Nappi AJ, Vass E (2002) Interactions of iron with reactive intermediates of oxygen and nitrogen. Dev Neurosci 24:134–142
Schürmann N, Forrer P, Casse O et al (2017) Myeloperoxidase targets oxidative host attacks to Salmonella and prevents collateral tissue damage. Nature Microbiol 2:16268
Klebanoff SJ (2005) (2005) Myeloperoxidase: friend and foe. J Leukoc Biol 77:598–625
Segal AW (2005) How neutrophils kill microbes. Annu Rev Immunol 23:197–223
Brovkovych V, Gao X-P, Ong E et al (2008) Augmented inducible nitric oxide synthase expression and increased NO production reduce sepsis-induced lung injury and mortality in myeloperoxidase-null mice. Am J Physiol Lung Cell Mol Physiol 295:L96–L103
Maslov AK (2000) Phagocytic myeloperoxidase in leprosy pathogenesis. Int J Lepr Other Mycobact Dis 68(1):71–73
Maslov AK, Luzhnova AS (2000) Effects of peroxidase therapy on functional state of the liver and phagocytes and blood cell counts in mice with experimental leprosy. Bull Exp Biol Med 130(1):682–686
Escorza MAQ, Salinas JVC (2009) La capacidad antioxidante total. Bases y aplicaciones REB 28:89–101
França-Botelho AC, França EL, Honório-França AC et al (2006) (2006) Phagocytosis of Giardia lamblia trophozoites by human colostral leukocytes. Acta Paediatr 95:438–443
Hii CS (2007) Ferrante A (2007) Regulation of the NADPH oxidase activity and anti-microbial function of neutrophils by arachidonic acid. Arch Immunol Ther Exp 55:99–110
Gozalo AS, Hofmann VJ, Brinster LR et al (2010) Spontaneous Staphylococcus xylosus infection in mice deficient in NADPH oxidase and comparison with other laboratory mouse strains. J Am Assoc Lab Anim Sci 49:480–486
Holland SM (2010) (2010) Chronic granulomatous disease. Clin Rev Allerg Immunol 38:3–10
Rojas-Espinosa (2009) Chapter 4: Murine leprosy revisited. In: Tomioka H (ed) Current topics on the profiles of host immunological response to Mycobacterial infections. Kerala, India, Research SignPost, pp 97–140
Chieber M, Chandel NS (2014) ROS function in redox signaling and oxidative stress. Curr Biol 24(10):R453–R462
Yang Y, Bazhin AV, Werner J, Karakhanova S (2013) Reactive oxygen species in the immune system. Int Rev Immunol 32(3):249–270
Dupnik KM, Bair TB, Maia AO et al (2015) Transcriptional changes that characterize the immune reactions of leprosy. J Infect Dis 211:1658–1676
Guerreiro LT, Robottom-Ferreira AB, Ribeiro-Alves M et al (2013) Gene expression profiling specifies chemokine, mitochondrial and lipid metabolism signatures in leprosy. PLoS One 8(6):e64748. https://doi.org/10.1371/journal.pone.0064748
Ramos GB, Salomão H, Francio AS, Fava VM, Werneck RI, Mira MT (2016) Association analysis suggests SOD2 as a newly Identified candidate gene associated with leprosy susceptibility. J Infect Dis 214(3):475–478
Lastória JC, de Abreu MAMM (2014) Leprosy: review of the epidemiological, clinical and etiopathogenetic aspects- part 1. An Bras Dermatol 89(2):205–218
Launois P, Blum L, Dieye A, Milan J, Sarthou JL, Bach MA (1989) Phenolic glycolipid-1 from M. leprae inhibits oxygen free radical production by human mononuclear cells. Res Immunol 140(9):847–855
Vachula M, Holzer TJ, Andersen BR (1989) Suppression of monocyte oxidative response by phenolic glycolipid I of Mycobacterium leprae. J Immunol 142(5):1696–1701
Cambier CJ, O’Leary SM, O’Sullivan MP, Keane J, Ramakrishnan L (2017) Phenolic glycolipid facilitates mycobacterial escape from microbicidal tissue-resident macrophages. Immunity 47:552–565
Madigan CA, Cambier CJ, Kelly-Scumpia KM, Sagasti A, Modin RL, Ramakrishnan L (2017) Phenolic glycolipid initiates nerve damage in leprosy. Cell 170:973–985
Mattos KA, Sarno EN, Pessolani MCV, Bozza PT (2012) Deciphering the contribution of lipid droplets in leprosy: multifunctional organelles with roles in Mycobacterium leprae pathogenesis. Mem Inst Oswaldo Cruz 107(suppl.1):156–166
WHO (1994) Chemotherapy of leprosy. Technical report series 847. World Health Organization, Geneva
Jyothi P, Riyaz N, Nandakumar G, Binitha MP (2008) A study of oxidative stress in paucibacillary and multibacillary leprosy. Indian J Dermatol Venereol Leprol 74(1):80
Bhadwat VR, Borade VB (2000) Increased lipid peroxidation in lepromatous leprosy. Indian J Dermatol Venereol Leprol 66(3):121–125
Reddy YN, Murthy SV, Krishna DR, Prabhakar MC (2003) Oxidative stress and anti-oxidant status in leprosy patients. Indian J Lepr 75(4):307–316
Vijayaraghavan R, Suribabu CS, Sekar B et al (2005) Protective role of vitamin E on the oxidative stress in Hansen’s disease (leprosy) patients. Eur J Clin Nutr 59(10):1121–1128
Chhabra N, Bhattacharya SN, Singal A, Ahmed RS, Verma P (2015) Profile of oxidative stress in response to treatment for type 1 reaction. Lepr Ver 86:80–88
Schalcher TR, Borges RS, Coleman MD et al (2014) Clinical oxidative stress during leprosy multidrug therapy: impact of dapsone oxidation. PLoS One 9(1):e85712. https://doi.org/10.1371/journal.pone.0085712
Prasad CV, Kodiwadmath MV, Kodiwadmath GB (2007) Erythrocyte superoxide dismutase, catalase activities and hydrogen peroxide induced lipid peroxidation in leprosy. Lepr Rev 78(4):391–397
Prasad CV, Kodiwadmath MV, Kodiwadmath GB (2008) Erythrocyte glutathione peroxidase, glutathione reductase activities and blood glutathione content in leprosy. J Infect 56(6):469–473
Abdel-Hafez HZ, Mohamed E-EM, Abd-Elghany AA (2010) Tissue and blood superoxide dismutase activity and malondialdehyde level in leprosy. J Eur Acad Dermatol Venereol 24(6):704–708
Patni V, Baliga S, Sawal S (2015) Saliva as a diagnostic tool for measurement of total antioxidant capacity in children with leprosy and Born to leprosy parent. Indian J Lepr 87(1):17–21
Lima ES, Roland IA, Maroja MF, Marcon JL (2007) Vitamin A and lipid peroxidation in patients with different forms of leprosy. Rev Inst Med Trop S. Paulo 49(4):211–214
Osadolor HB, Ihongbe JC (2008) Effect of leprosy on non-enzymatic antioxidants (vitamin C, vitamin E and uric acid) in (Edo State) Nigerian leprosy patients. Cont J Biomed Sci 2:1–5
Asalkar A, Girish S, Naoley R (2011) Protein oxidation and antioxidant vitamins in leprosy. Int J Pharm Sci Res 2(11):2870–2873
Prabhakar MC, Santhikrupa D, Manasa N, Rao OU (2013) Status of free radicals and antioxidants in leprosy patients. Indian J Lepr 85(1):5–9
Swathi M, Tagore R (2015) Study of oxidative stress in different forms of leprosy. Indian J Dermatol 60(3):321
Benzie IFF, Strain JJ (1996) The ferric reducing ability of plasma (FRAP) as a measure of “Antioxidant Power”: the FRAP assay. Anal Biochem 239:70–76
Re R, Pellegrini N, Proteggente A, Pannala A, Yang M, Rice-Evans C (1999) Antioxidant activity applying an improved ABTS radical cation decolorization assay. Free Rad Biol Med 26(9/10):1231–1237
Bowman GL, Shannon J, Frei B, Kaye JA, Quinn JF (2010) Uric acid as a CNS antioxidant. J Alzheim Dis 19(4):1331–1336
El Ridi R, Tallima H (2017) Physiological functions and pathogenic potential of uric acid: a review. J Adv Res 8:487–493
Waring WS, Webb DJ, Maxwell SRJ (2001) Systemic uric acid administration increases serum antioxidant capacity in healthy volunteers. J Cardiovasc Pharmacol 38:365–371
Barsoum R, El-Khatib M (2017) Uric acid and life on earth. J Adv Res 8:471–474
Sautin YY, Nakagawa T, Zharikov S, Johnson RJ (2007) Adverse effects of the classic antioxidant uric acid in adipocytes: NADPH oxidase-mediated oxidative/nitrosative stress. Am J Physiol Cell Physiol 293(2):C584–C596
Sautin YY, Johnson RJ (2008) Uric acid: the oxidant-antioxidant paradox. Nucleos Nucleot Nucleic Acid 27(6):608–619
Morato-Conceiçao YT, Alves-junior ER, Arruda TA, Lopes JC, Fontes CJF (2016) Serum uric acid levels during leprosy reaction episodes. Peer J 4:4e1799. https://doi.org/10.7717/peerj.1799
Schalcher TR, Vieira JLF, Salgado CG, Borges RS, Monteiro MC (2013) Antioxidant factors, nitric oxide levels, and cellular damage in leprosy patients. Rev Soc Bras Med Trop 46(5):645–649
Raka I, Rastogi MK, Gahalaut P, Kaur J, Mishra N (2018) Enzymatic oxidative stress indicators and oxidative stress índex in patients of leprosy. Nepal J Dermatol Venereol Leprol 16(1):35–40
Elesawy FM, Mikhael NW, Sabry JH (2015) Serum nitric oxide metabolites in leprosy patients as a parameter of prognostic value. J Egypt Women Dermatol Soc 12:44–48
Abd-Elmaged WM, Hassan MH, Mostafa MA, Ahmed NS, Samy ES (2017) Lesional levels of superoxide dismutase and malondialdehyde in paucibacillary and multibacillary leprosy patients. J Egypt Women Dermatol Soc 14:156–160
Pradhan T, Kumari S (2015) Evaluation of oxidative status and zinc level in leprosy patients after zinc supplementation. Int J Biol Med Res 6(2):4984–4987
Oliveira FM, Barbosa Junior F, Jordão Junior AA, Foss NT, Navarro AM, Frade MAC (2015) Oxidative stress and micronutrients in leprosy. Rev Nutr 28(4):349–357
Partogi D, Dalimunthe DA, Hazlianda CP (2018) A study of Selenium in leprosy. Macedonian J Med Sci 6(3):485–487
Vázquez CMP, Mendes Netto RS, Barbosa KBF et al (2014) Micronutrients influencing the immune response in leprosy. Nutr Hosp 29(1):26–36
Ferrari CKB (2005) Minerals. From basic aspects to newly discovered physiological and nutritional actions. Evid Based Integrat Med 2(3):123–131
Rayman MP (2012) Selenium and human health. Lancet 379(9822):1256–1268
Ferrari CKB (2014) Nutrição, saúde e longevidade baseadas em evidências científicas. Plêiade 8(15):26–36
Arias ARL, Santos VG (2008) Metalotioneína: processos celulares e moleculares. Cad Saúde Col 16(4):701–716
Jarosz M, Olbert M, Wyszogrodzka G, Mlyniec K, Librowski T (2017) Antioxidant and anti-inflammatory effects of zinc. Zinc-dependent NF-ĸB signaling. Inflammopharmacology 25(1):11–24
Wessels I, Maywald M, Rink L (2017) Zinc as a gatekeeper of immune function. Nutrients 9(12):1286. https://doi.org/10.3390/nu9121286
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Nature Singapore Pte Ltd.
About this chapter
Cite this chapter
Ferrari, C.K.B. (2019). Oxidative Stress and Antioxidant Supplementation on Immunity in Hansen’s Disease (Leprosy). In: Chakraborti, S., Chakraborti, T., Chattopadhyay, D., Shaha, C. (eds) Oxidative Stress in Microbial Diseases. Springer, Singapore. https://doi.org/10.1007/978-981-13-8763-0_18
Download citation
DOI: https://doi.org/10.1007/978-981-13-8763-0_18
Published:
Publisher Name: Springer, Singapore
Print ISBN: 978-981-13-8762-3
Online ISBN: 978-981-13-8763-0
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)