Zusammenfassung
Der Verlauf von Infektionen wird durch Reaktionen zwischen Erreger- und Wirtsstrukturen bestimmt. Zahlreiche Reaktionen dieser Art finden zwischen spezialisierten Abwehrmolekülen des Wirts wie z. B. Antikörpern und zufällig beteiligten Erregerstrukturen statt. Ihnen stehen andere gegenüber, die vom Erreger ausgehen. Moleküle des Erregers reagieren dabei selektiv mit Zielmolekülen des Wirts, meist um Invasion, Vermehrung oder Persistenz des Erregers zu vermitteln. Eine große Zahl solcher Erregermoleküle sind bereits als Pathogenitätsfaktoren identifiziert und charakterisiert; sie alle zu beschreiben würde den Rahmen dieses Kapitels sprengen. Gleichermaßen von Interesse sind bei dieser Art Reaktionen die Partner auf Seiten des Wirts. Dies sind in der Regel Moleküle, die für die Entwicklung der Infektionserreger von essentieller Bedeutung sind.
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 subscriptionsPreview
Unable to display preview. Download preview PDF.
Literatur
Abel L, Demenais F (1988) Detection of major genes for susceptibility to leprosy and its subtypes in a Carribean island: Desirade island. Am J Hum Genet 42:256–266
Abel L, Dessein AJ (1997) The impact of host genetics on susceptibility to human infectious diseases. Curr Opin Immunol 9:509–516
Abel L, Demenais F, Prata A, Souza AE, Dessein A (1991) Evidence for the segregation of a major gene in human susceptibility/resistance to infection by Schistosoma man-soni. Am J Hum Genet 48:959–970
Abel L, Vu DL, Oberti J, Nguyen VT, Van VC, Guilloud-Bataille M, Schurr E, Lagrange PH (1995) Complex segregation analysis of leprosy in southern Vietnam. Genet Epidemiol 12:63–82
Amiri P, Locksley RM, Parslow TG, Sadick M, Rector E, Ritter D, McKerrow JH (1992) Tumour necrosis factor a restores granulomas and induces egg-laying in schistosome-infected SCID mice. Nature 356:604–607
Anderson R, Wang S, Osiowy C, Issekutz AC (1997) Activation of endothelial cells via antibody-enhanced Dengue virus infection of peripheral blood monocytes. J Virol 71:4.226–4.232
Berendt AR, Simmons DL, Tansey J, Newbold CI, Marsh K (1989) Intercellular adhesion molecule-1 is an endothelial cell adhesion receptor for Plasmodium falciparum. Nature 341:57–59
Beutler E (1994) G6PD deficiency. Blood 84:3.613–3.636
Bienzle U, Ayeni O, Lucas AO, Luzzatto L (1972) Glucose-6-phosphate dehydrogenase and malaria. Greater resistance of females heterozygous for enzyme deficiency and of males with non-deficient variant. Lancet 1:107–110
Blackwell JM (1996) Genetic susceptibility to leishmanial infections: studies in mice and man. Parasitology 112:S67–S74
Bradley DJ (1974) Genetic control of natural resistance to Leishmania donovani. Nature 250:353–354
Cabrera M, Shaw M-A, Sharpies C, Williams H, Castes M, Convit J, Blackwell JM (1995) Polymorphism in tumor necrosis factor genes associated with mucocutaneous leishmaniasis. J Exp Med 182:1259–1264
Cattani JA, Gibson FD, Alpers MP, Crane GG (1987) Hereditary ovalocytosis and reduced susceptibility to malaria in Papua New Guinea. Trans R Soc Trop Med Hyg 81:705–709
Cerami C, Frevert U, Sinnis P, Takacs B, Clavijo P, Santos MJ, Nussenzweig V (1992) The basolateral domain of the hepatocyte plasma membrane bears receptors for the circumsporozoite protein of Plasmodium falciparum sporozoites. Cell 70:1021–1033
Chan J, Fujiwara T, Brennan P, McNeil M, Turco SJ, Sibille J-C, Snapper M, Aisen P, Bloom BR (1989) Microbial glycolipids: possible virulence factors that scavenge oxygen radicals. Proc Natl Acad Sci USA 86:2.453–2.457
Chang K-P, Chaudhuri G, Fong D (1990) Molecular determinants of Leishmania virulence. Annu Rev Microbiol 44:499–529
Chen Y, Maguire T, Hileman RE, Fromm JR, Esko JD, Linhardt RJ, Marks RM (1997) Dengue virus infectivity depends on envelope protein binding to target cell heparan sulfate. Nat Med 3:866–871
Choudhuri A, Polyakova J, Zbrzezna V, Williams K, Gulati S, Pogo AO (1993) Cloning of glycoprotein D cDNA, which encodes the major subunit of the Duffy blood group system and the receptor for the Plasmodium vivax malaria parasite. Proc Natl Acad Sci USA 90:10.793–10.797
De Vries RRP (1992) HLA and disease: from epidemiology to immunotherapy. Eur J Clin Invest 22:1–8
Desjardins M, Descoteaux A (1997) Inhibition of phagolysosomal biogenesis by the leishmania lipophosphoglycan. J Exp Med 185:2.061–2.068
Dolan SA, Proctor JL, Alling DW, Okubo Y, Wellems TE, Miller LH (1994) Glycophorin B as an EBA-175 independent Plasmodium falciparum receptor of human erythrocytes. Mol Biochem Parasitol 64:55–63
Field M, Rao MC, Chang EB (1989) Intestinal electrolyte transport and diarrheal disease. N Engl J Med 321:800–806
Field SP, Hempelmann E, Mendelow BV, Fleming AF (1994) Glycophorin variants and Plasmodium falciparum :protective effect of the Dantu phenotype in vitro. Hum Genet 93:148–150
Fraser GR, Giblett ER, Motulsky AG (1966) Population genetic studies in the Congo. III. Blood groups (ABO, MNSs, Rh, Jsa). Am J Hum Genet 18:546–552
Frevert U, Sinnis P, Cerami C, Shreffler W, Takacs B, Nussenzweig V (1993) Malaria circumsporozoite protein binds to heparin sulfate proteoglycans associated with the surface membrane of hepatocytes. J Exp Med 177:1287–1298
Gorham JD, Güler ML, Steen RG, Mackey AJ, Daly MJ, Frederick K, Dietrich WF, Murphy KM (1996) Genetic mapping of a murine locus controlling development of T helper 1/T helper 2 type responses. Proc Natl Acad Sci USA 93:12.467–12.472
Hagan P, Blumenthal UJ, Dunn D, Simpson AJG, Wilkins HA (1991) Human IgE, IgG4 and resistance to reinfection with Schistosoma haematobium. Nature 349:243–245
Haidane JBS (1949) Disease and evolution. Hereditas 35:S267–S273
Hatzigeorgiou DE, Geng J, Zhu B, Zhang Y, Liu K, Rom WN, Fenton MJ, Turco SJ, Ho JL (1996) Lipophosphoglycan from Leishmania suppresses agonist-induced interleukin 1β gene expression in human monocytes via a unique promoter sequence. Proc Natl Acad Sci USA 93:14.708–14.713
Higgs DR, Vickers MA, Wilkie AOM, Pretorius IM, Jarman AP, Weatherall DJ (1989) A review of the molecular genetics of the human α-globin gene cluster. Blood 73:1081–1104
Hill AVS, Allsopp CEM, Kwiatkowski D, Anstey NM, Twumasi P, Rowe PA, Bennett S, Brewster D, McMichael AJ, Greenwood BM (1991) Common West African HLA antigens are associated with protection from severe malaria. Nature 352:595–600
Hill AVS, Elvin J, Willis AC, Aidoo M, Allsopp CEM, Gotch FM, Gao XM, Takiguchi M, Greenwood BM, Townsend AM, McMichael AJ, Whittle EHC (1992) Molecular analysis of the association of HLA-B53 and resistance to severe malaria. Nature 360:434–439
Holmgren J, Clemens J, Sack DA, Svernnerholm A-M (1989) New cholera vaccines. Vaccine 7:94–96
Horuk R, Chitnis CE, Darbonne WC, Colby TJ, Rybicki A, Hadley TJ, Miller LH (1993) A receptor for the malarial parasite Plasmodium vivax :The erythrocyte chemokine receptor. Science 261:1182–1184
Huisman TH (1993) The structure and function of normal and abnormal haemoglobins. Baillieres Clin Haematol 6:1–30
Jarolim P, Palek J, Amato D, Hassan K, Sapak P, Nurse GT, Rubin HL, Zhai S, Sahr KE, Liu S-C (1991) Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis. Proc Natl Acad Sci USA 88:11022–11026
Kemp SJ, Iraqi F, Darvasi A, Soller M, Teale AJ (1997) Localization of genes controlling resistance to trypanosomiasis in mice. Nat Genet 16:194–196
Lara ML, Layrisse Z, Scorza JV, Garcia E, Stoikow Z, Granados J, Bias W (1991) Immunogenetics of human American cutaneous leishmaniasis. Study of HLA haplotypes in 24 families from Venezuela. Hum Immunol 30:129–135
Liu S-C, Zhai S, Palek J, Golan DE, Amato D, Hassan K, Nurse GT, Babona D, Coetzer T, Jarolim P, Zaik M, Borwein S (1990) Molecular defect of the band 3 protein in southeast Asian ovalocytosis. N Engl J Med 323:1530–1538
Liu J, Fujiwara TM, Buu NT, Sanchez FO, Cellier M, Paradis AJ, Frappier D, Skamene E, Gros P, Morgan K, Schurr E (1995) Identification and sequence variants in the human homologue of the mouse natural resistance-associated macrophage protein gene. Am J Hum Genet 56:845–853
Marsh DG, Neely JD, Breazeale DR, Gosh B, Freidhoff LR, Ehrlich-Kautzky E, Schou C, Krishnaswamy G, Beaty TH (1994) Linkage analysis of IL4 and other chromosome 5q31.1 markers and total serum immunoglobulin E concentrations. Science 264:1152–1156
McGuire W, Hill AVS, Allsopp CEM, Greenwood BM, Kwiatkowski D (1994) Variation in the TNF-α promoter region associated with susceptibility to cerebral malaria. Nature 371:508–511
Mekalanos JJ (1985) Cholera toxin: Genetic analysis, regulation, and role in pathogenesis. Curr Top Microbiol Immunol 118:97–118
Miller LH (1994) Impact of malaria on genetic polymorphism and genetic disease in Africans and African Americans. Proc Natl Acad Sci USA 91:2.415–2.419
Miller LH, Good MF, Milon G (1994) Malaria pathogenesis. Science 264:1878–1883
Ming M, Ewen ME, Pereira MEA (1995) Trypanosome invasion of mammalian cells requires activation of the TGFβ signaling pathway. Cell 82:287–296
Mock BA, Krall MM, Byrd LG, Chin H, Barton CH, Charles I, Liew FY, Blackwell JM (1994) The inducible form of nitric oxide synthase (NOS2) isolated from murine macrophages maps near the nude mutation on mouse chromosome 11. Eur J Immunogenet 21:231–238
Montgomery RI, Warner MS, Lum BJ, Spear PG (1996) Herpes simplex virus-1 entry into cells mediated by a novel member of the TNF/NGF receptor family. Cell 87:427–436
Mosmann TR, Coffman RL (1989) Heterogeneity of cytokine secretion patterns and functions of helper T cells. Adv Immunol 46:111–147
Mosser DM, Edelson PJ (1987) The third component of complement (C3) is responsible for intracellular survival of Leishmania major. Nature 327:329–331
Müller-Myhsok B, Stelma FF, Guisse-Sow F, Muntau B, Thye T, Burchard GD, Gryseels B, Horstmann RD (1997) Further evidence suggesting the presence of a locus on human chromosome 5q31-q33 influencing the intensity of infection with Schistosoma mansoni. Am J Hum Genet 61:452–454
Ortega-Barria E, Pereira MEA (1991) A novel T. cruzi heparin-binding protein promotes fibroblast adhesion and penetration of engineered bacteria and trypanosomes into mammalian cells. Cell 67:411–421
Pancake SJ, Holt GD, Mellouk S, Hoffman SL (1992) Malaria sporozoites and circumsporozoite proteins bind specifically to sulfated glycoconjugates. J Cell Biol 117:1351–1357
Pauling L, Itano H, Singer SJ, Wells, IC (1949) Sickle cell anaemia: A molecular disease. Science 110:543–546
Pereira MEA (1983) A developmentally regulated neuraminidase activity in Trypanosoma cruzi. Science 219:1444–1446
Plant J, Glynn AA (1974) Natural resistance to Salmonella infection, delayed hypersensitivity and Ir genes in different strains of mice. Nature 248:345–347
Postma DS, Bleecker ER, Amelung PJ, Holroyd KJ, Xu J, Panhuysen CIM, Meyers DA, Levitt RC (1995) Genetic susceptibility to asthma — bronchial hyperresponsiveness coinherited with a major gene for atopy. N Engl J Med 333:894–900
Proudfoot L, Nikolaev AV, Feng G-J, Wei X-Q, Ferguson MAJ, Brimacombe JS, Liew FY (1996) Regulation of the expression of nitric oxide synthase and leishmanicidal activity by glycoconjugates of Leishmania lipophosphoglycan in murine macrophages. Proc Natl Acad Sci USA 93:10.984–10.989
Ramabukkana A, Salzer JL, Yurchenco PD, Tuomanen EI (1997) Neural targeting of Mycobacterium leprae by the G domain of the laminin-α2 chain. Cell 88:811–821
Raulet DH (1994) MHC class I-deficient mice. Adv Immunol 55:381–421
Reid ME, Lomas-Francis C, Daniels GL, Chen V, Shen J, Ho YC, Hare V, Batts R, Yacob M, Smart E (1995) Expression of the erythrocyte antigen Henshaw (He; MNS6): serological and immunochemical studies. Vox Sang 68:183–186
Riley EM, Olerup O, Bennett S, Rowe P, Allen SJ, Blackman MJ, Troye-Blomberg M, Holder AA, Greenwood BM (1992) MHC and malaria: the relationship between HLA class II alleles and immune responses to Plasmodium falciparum. Int Immunol 4:1055–1063
Roberts DJ, Biggs B-A, Brown G, Newbold CI (1993) Protection, pathogenesis and phenotypic plasticity in Plasmodium falciparum malaria. Parasitol Today 9:281–286
Roberts LJ, Baldwin TM, Curtis JM, Handman E, Foote SJ (1997) Resistance to Leishmania major is linked to the H2 region on chromosome 17 and to chromosome 9. J Exp Med 185:1705–1710
Robson KJH, Hall JRS, Jennings MW, Harris TJR, Marsh K, Newbold CI, Tate VE, Weatherall DJ (1988) A highly conserved amino-acid sequence in thrombospondin, properdin and in proteins from sporozoites and blood stages of a human malaria parasite. Nature 335:79–82
Rostand KS, Esko JD (1997) Microbial adherence to and invasion through proteoglycans. Infect Immun 65:1–8
Ruwende C, Khoo SC, Snow RW, Yates SNR, Kwiatkowski D, Gupta S, Warn P, Allsopp CEM, Gilbert SC, Peschu N, Newbold CI, Greenwood BM, Marsh K, Hill AVS (1995) Natural selection of hemi- and heterozygotes for G6PD deficiency in Africa by resistance to severe malaria. Nature 376:246–249
Schenkman S, Jiang M-S, Hart GW, Nussenzweig V (1991) A novel cell surface trans-sialidase of Trypanosoma cruzi generates a stage-specific epitope required for invasion of mammalian cells. Cell 65:1117–1125
Schlesinger LS (1993) Macrophage phagocytosis of virulent but not attenuated strains of Mycobacterium tuberculosis is mediated by mannose receptors in addition to complement receptors. J Immunol 150:2.920–2.930
Schlesinger LS, Horwitz MA (1991) Phagocytosis of Mycobacterium leprae by human monocyte-derived macrophages is mediated by complement receptors CR1 (CD35), CR3 (CD11b/CD18), and CR4 (CD11c/CD18) and IFNγ activation inhibits complement receptor function and phagocytosis of this bacterium. J Immunol 147:1983–1994
Schorey JS, Li Q, McCourt DW, Bong-Mastek M, Clark-Curtiss JE, Ratliff TL, Brown EJ (1995) A Mycobacterium leprae gene encoding a fibronectin binding protein is used for efficient invasion of epithelial cells and Schwann cells. Infect Immun 63:2.652–2.657
Schorey JS, Carroll MC, Brown EJ (1997) A macrophage invasion mechanism of pathogenic mycobacteria. Science 277:1091–1093
Shakibaei M, Frevert U (1996) Dual interaction of the malaria circumsporozoite protein with low density lipoprotein receptor-related protein (LRP) and heparan sulfate proteoglycans. J Exp Med 184:1699–1711
Sim BKL, Chitnis CE, Wasniowska K, Hadley TJ, Miller LH (1994) Receptor and ligand domains for invasion of erythrocytes by Plasmodium falciparum. Science 264:1941–1944
Sixma TK, Pronk SE, Kalk KH, Wartna ES, Zanten BAM van, Witholt B, Hol WGJ (1991) Crystal structure of a cholera toxin-related heat-labile enterotoxin from E. coli. Nature 351:371–377
Smith JD, Chitnis CE, Craig AG, Roberts DJ, Hudson-Taylor DE, Peterson DS, Pinches R, Newbold CI, Miller LH (1995) Switches in expression of Plasmodium falciparum var genes correlate with changes in antigenic and cytoadherent phenotypes of infected erythrocytes. Cell 83:101–110
Spangler BD (1992) Structure and function of cholera toxin and the related Escherichia coli heat-labile enterotoxin. Microbiol Rev 56:622–647
Springer TA (1994) Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm. Cell 76:301–314
Su X-Z, Heatwole VM, Wertheimer SP, Guinet F, Herrfeldt JA, Peterson DS, Ravetch JA, Wellems TE (1995) The large diverse gene family var encodes proteins involved in cytoadherence and antigenic variation of Plasmodium falciparum-infected erythrocytes. Cell 82:89–100
Tarleton RL, Koller BH, Latour A, Postan M (1992) Susceptibility of β 2-microglobulin-deficient mice to Trypanosoma cruzi infection. Nature 356:338–340
Turco SJ, Descoteaux A (1992) The lipophosphoglycan of Leishmania parasites. Annu Rev Microbiol 46:65–94
Unger P, Procter JL, Moulds JJ, Moulds M, Blanchard D, Guizzo MC, McCall LA, Cartron JP, Dahr W (1987) The Dantu erythrocyte phenotype of the NE variety. II. Serology, immunochemistry, genetics, and frequency. Blut 55:33–43
Vachula M, Holzer TJ, Anderson BR (1989) Suppression of monocyte oxidative response by phenolic glycolipid I of Mycobacterium leprae. J Immunol 142:1696–1701
Vidal SM, Malo D, Vogan K, Skamene E, Gros P (1993) Natural resistance to infection with intracellular parasites: isolation of a candidate for bcg. Cell 73:469–485
Wei X, Charles IG, Smith A, Ure J, Feng G, Huang F, Xu D, Muller W, Moncada S, Liew FY (1995) Altered immune response in mice lacking inducible nitric oxide synthase. Nature 375:408–411
WHO (1993) Public health impact of schistosomiasis. Bull WHO 71:657–662
Williams TN, Maitland K, Bennett S, Ganczakowski M, Peto TEA, Newbold CI, Bowden DK, Weatherall DJ, Clegg JB (1996) High incidence of malaria in α-thalassaemic children. Nature 383:522–525
Wilson AG, Symons JA, McDowell TL, McDevitt HO, Duff GW (1997) Effects of a polymorphism in the human tumor necrosis factor a promoter on transcriptional activation. Proc Natl Acad Sci USA 94:3.195–3.199
Zerva L, Cizman B, Mehra NK, Alahari SK, Murali R, Zmijewski CM, Kamoun M, Monos DS (1996) Arginine at positions 13 or 70–71 in pocket 4 of HLA-DRB1 alleles is associated with susceptibility to tuberculoid leprosy. J Exp Med 183:829–836
Zhang G, Liu Y, Ruoho AE, Hurley JH (1997) Structure of the adenylyl cyclase catalytic core. Nature 386:247–253
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 1999 Springer-Verlag Berlin Heidelberg
About this chapter
Cite this chapter
Horstmann, R.D. (1999). Infektionskrankheiten: Tropenmedizinische Aspekte. In: Ganten, D., Ruckpaul, K. (eds) Immunsystem und Infektiologie. Handbuch der Molekularen Medizin, vol 4. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-07865-5_9
Download citation
DOI: https://doi.org/10.1007/978-3-662-07865-5_9
Publisher Name: Springer, Berlin, Heidelberg
Print ISBN: 978-3-662-07866-2
Online ISBN: 978-3-662-07865-5
eBook Packages: Springer Book Archive