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Human Genetics of Infectious Diseases

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Vogel and Motulsky's Human Genetics

Abstract

A lingering question in the field of infectious diseases is that of the considerable clinical variability between individuals in the course of infection, raising fundamental questions about the actual pathogenesis of infectious diseases. There is increasing epidemiological and experimental evidence to suggest that human genetics plays a major role in susceptibility/resistance to infectious diseases. There seems to be a continuous spectrum of human predisposition to infectious diseases, from monogenic to polygenic inheritance. Many monogenic primary immunodeficiencies have been clinically described and genetically deciphered, and most predispose affected individuals to multiple infections. Other monogenic traits conferring patho-gen-specific susceptibility in otherwise healthy individuals are increasingly being described. Examples of Mendelian specific resistance to infectious agents are also being discovered. At the population level, major genes are being identified in a small, but growing number of common infectious diseases. Truly polygenic predisposition to a human infectious disease remains to be definitively demonstrated experimentally, despite the unquestionable identification of individual (but not necessarily interacting) susceptibility genes. Studies of the human genetics of infectious diseases have considerable clinical implications, as improvements in our understanding of the pathogenesis of infectious disease pave the way to both genetic diagnosis and immu-nological interventions. The genetic investigation of infectious diseases, seen as ‘experiments of Nature’, also provides a unique approach to definition of the function of host defense genes in natura — i.e. in the setting of a natural, as opposed to experimental, ecosystem governed by natural selection.

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References

  1. Abel L, Casanova JL (2000) Genetic predisposition to clinical tuberculosis: bridging the gap between simple and complex inheritance. Am J Hum Genet 67:274–277

    Article  CAS  PubMed  Google Scholar 

  2. Abel L, Demenais F (1988) Detection of major genes for susceptibility to leprosy and its subtypes. Am J Hum Genet 42:256–266

    CAS  PubMed  Google Scholar 

  3. 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

    Article  CAS  PubMed  Google Scholar 

  4. Alcais A, Abel L (2004) Application of genetic epidemiology to dissecting host susceptibility/resistance to infection illustrated with the study of common mycobacterial infections. In: Bellamy R (ed) Susceptibility to infectious diseases: the importance of host genetics. Cambridge University Press, Cambridge, pp 7–44

    Google Scholar 

  5. Alcais A, Alter A, Antoni G, Orlova M, Thuc NV, Singh M, Vanderborght PR, Katoch K, Mira MT, Thai VH, Huong NT, Ba NN, Moraes M, Mehra N, Schurr E, Abel L (2007) Stepwise replication identifies a low-producing lymphoto-xin-alpha allele as a major risk factor for early-onset leprosy. Nat Genet 39:517–522

    Article  CAS  PubMed  Google Scholar 

  6. Alcais A, Mira M, Casanova JL, Schurr E, Abel L (2005) Genetic dissection of immunity in leprosy. Curr Opin Immunol 17:44–48

    Article  CAS  PubMed  Google Scholar 

  7. Allison AC (1954) Protection afforded by sickle cell trait against subtertian malarian infection. Br Med J 1:290–294

    Article  CAS  PubMed  Google Scholar 

  8. Antonarakis SE, Beckmann JS (2006) Mendelian disorders deserve more attention. Nat Rev Genet 7:277–282

    Article  CAS  PubMed  Google Scholar 

  9. Arenzana-Seisdedos F, Parmentier M (2006) Genetics of resistance to HIV infection: role of co-receptors and co-receptor ligands. Semin Immunol 18:387–403

    Article  CAS  PubMed  Google Scholar 

  10. Baghdadi JE, Orlova M, Alter A, Ranque B, ChentoufiM, Lazrak F, Archane MI, Casanova JL, Benslimane A, Schurr E, Abel L (2006) An autosomal dominant major gene confers predisposition to pulmonary tuberculosis in adults. J Exp Med 203:1679–1684

    Article  PubMed  CAS  Google Scholar 

  11. Barnwell JW, Nichols ME, Rubinstein P (1989) In vitro evaluation of the role of the Duffy blood group in erythro-cyte invasion by Plasmodium vivax. J Exp Med 169:1795–1802

    Article  CAS  PubMed  Google Scholar 

  12. Bellamy R, Ruwende C, Corrah T, McAdam KPWJ, Whittle HC, Hill AVS (1998) Variations in the NRAMP1 gene and susceptibility to tuberculosis in west africans. New Engl J Med 338:640–644

    Article  CAS  PubMed  Google Scholar 

  13. von Bernuth H, Picard C, Jin Z, Pankla R, Xiao H, Ku CL, Chrabieh M, Mustapha IB, Ghandil P, Camcioglu Y, Vasconcelos J, Sirvent N, Guedes M, Vitor AB, Herrero-Mata MJ, Aróstegui JI, Rodrigo C, Alsina L, Ruiz-Ortiz E, Juan M, Fortuny C, Yagüe J, Antón J, Pascal M, Chang HH, Janniere L, Rose Y, Garty BZ, Chapel H, Issekutz A, Maródi L, Rodriguez-Gallego C, Banchereau J, Abel L, Li X, Chaussabel D, Puel A, Casanova JL (2008) Pyogenic bacterial infections in humans with MyD88 deficiency. Science 321(5889):691–696

    Article  CAS  Google Scholar 

  14. Bertrand Y, Muller SM, Casanova JL, Morgan G, Fischer A, Friedrich W (2002) Reticular dysgenesis: HLA non-identical bone marrow transplants in a series of 10 patients. Bone Marrow Transplant 29:759–762

    Article  CAS  PubMed  Google Scholar 

  15. Brown KE, Hibbs JR, Gallinella G, Anderson SM, Lehman ED, McCarthy P, Young NS (1994) Resistance to parvovirus B19 infection due to lack of virus receptor (erythrocyte P antigen). N Engl J Med 330:1192–1196

    Article  CAS  PubMed  Google Scholar 

  16. Bruton OC (1952) Agammaglobulinemia. Pediatrics 9:722–728

    CAS  PubMed  Google Scholar 

  17. Bruton OC (1962) A decade with agammaglobulinemia. J Pediatr 60:672–676

    Article  CAS  PubMed  Google Scholar 

  18. Casanova JL, Abel L (2002) Genetic dissection of immunity to mycobacteria: the human model. Annu Rev Immunol 20:581–620

    Article  CAS  PubMed  Google Scholar 

  19. Casanova JL, Abel L (2007) Human genetics of infectious diseases: a unified theory. Embo J 26:915–922

    Article  CAS  PubMed  Google Scholar 

  20. Casanova JL, Abel L (2004) The human model: a genetic dissection of immunity to infection in natural conditions. Nat Rev Immunol 4:55–66

    Article  CAS  PubMed  Google Scholar 

  21. Casanova JL, Abel L (2005) Inborn errors of immunity to infection: the rule rather than the exception. J Exp Med 202:197–201

    Article  CAS  PubMed  Google Scholar 

  22. Casanova JL, Abel L (2007) Primary immunodeficiencies: a field in its infancy. Science 317:617–619

    Article  CAS  PubMed  Google Scholar 

  23. Casanova JL, Fieschi C, Bustamante J, Reichenbach J, Remus N, von Bernuth H, Picard C (2005) From idiopathic infectious diseases to novel primary immunodeficiencies. J Allergy Clin Immunol 116:426–430

    Article  CAS  PubMed  Google Scholar 

  24. Casrouge A, Zhang SY, Eidenschenk C, Jouanguy E, Puel A, Yang K, Alcais A, Picard C, MahfoufiN, Nicolas N, Lorenzo L, Plancoulaine S, Senechal B, Geissmann F, Tabeta K, Hoebe K, Du X, Miller RL, Heron B, Mignot C, de Villemeur TB, Lebon P, Dulac O, Rozenberg F, Beutler B, Tardieu M, Abel L, Casanova JL (2006) Herpes simplex virus encephalitis in human UNC-93B deficiency. Science 314:308–312

    Article  CAS  PubMed  Google Scholar 

  25. Cavazzana-Calvo M, Hacein-Bey S, de Saint Basile G, Gross F, Yvon E, Nusbaum P, Selz F, Hue C, Certain S, Casanova JL, Bousso P, Deist FL, Fischer A (2000) Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. Science 288:669–672

    Article  CAS  PubMed  Google Scholar 

  26. Coffey AJ, Brooksbank RA, Brandau O, Oohashi T, Howell GR, Bye JM, Cahn AP, Durham J, Heath P, Wray P, Pavitt R, Wilkinson J, Leversha M, Huckle E, Shaw-Smith CJ, Dunham A, Rhodes S, Schuster V, Porta G, Yin L, Serafini P, Sylla B, Zollo M, Franco B, Bolino A, Seri M, Lanyi A, Davis JR, Webster D, Harris A, Lenoir G, de St Basile G, Jones A, Behloradsky BH, Achatz H, Murken J, Fassler R, Sumegi J, Romeo G, Vaudin M, Ross MT, Meindl A, Bentley DR (1998) Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene. Nat Genet 20:129–135

    Article  CAS  PubMed  Google Scholar 

  27. Dean M, Carrington M, Winkler C, Huttley GA, Smith MW, Allikmets R, Goedert JJ, Buchbinder SP, Vittinghoff E, Gomperts E, Donfield S, Vlahov D, Kaslow R, Saah A, Rinaldo C, Detels R, O'Brien SJ (1996) Genetic restriction of HIV-1 infection and progression to AIDS by a deletion allele of the CKR5 structural gene. Science 273:1856–1862

    Article  CAS  PubMed  Google Scholar 

  28. Dubos RJ (1950) Louis Pasteur, free lance of science, 1st edn. Little Brown, Boston

    Google Scholar 

  29. Duerr RH, Taylor KD, Brant SR, Rioux JD, Silverberg MS, Daly MJ, Steinhart AH, Abraham C, Regueiro M, Griffiths A, Dassopoulos T, Bitton A, Yang H, Targan S, Datta LW, Kistner EO, Schumm LP, Lee AT, Gregersen PK, Barmada MM, Rotter JI, Nicolae DL, Cho JH (2006) A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science 314:1461–1463

    Article  CAS  PubMed  Google Scholar 

  30. Edwards JH (1969) Familial predisposition in man. Br Med Bull 25:58–64

    CAS  PubMed  Google Scholar 

  31. Fellay J, Shianna K V, Ge D, Colombo S, Ledergerber B, Weale M, Zhang K, Gumbs C, Castagna A, Cossarizza A, Cozzi-Lepri A, De Luca A, Easterbrook P, Francioli P, Mallal S, Martinez-Picado J, Miro JM, Obel N, Smith JP, Wyniger J, Descombes P, Antonarakis SE, Letvin NL, McMichael AJ, Haynes BF, Telenti A, Goldstein DB (2007) A whole-genome association study of major determinants for host control of HIV-1. Science 317:944–947

    Article  CAS  PubMed  Google Scholar 

  32. Fieschi C, Dupuis S, Catherinot E, Feinberg J, Bustamante J, Breiman A, Altare F, Baretto R, Le Deist F, Kayal S, Koch H, Richter D, Brezina M, Aksu G, Wood P, Al-Jumaah S, Raspall M, Da Silva Duarte AJ, Tuerlinckx D, Virelizier JL, Fischer A, Enright A, Bernhoft J, Cleary AM, Vermylen C, Rodriguez-Gallego C, Davies G, Blutters-Sawatzki R, Siegrist CA, Ehlayel MS, Novelli V, Haas WH, Levy J, Freihorst J, Al-Hajjar S, Nadal D, De Moraes Vasconcelos D, Jeppsson O, Kutukculer N, Frecerova K, Caragol I, Lammas D, Kumararatne DS, Abel L, Casanova JL (2003) Low penetrance, broad resistance, and favorable outcome of interleukin 12 receptor beta1 deficiency: medical and immu-nological implications. J Exp Med 197:527–535

    Article  CAS  PubMed  Google Scholar 

  33. Filipe-Santos O, Bustamante J, Chapgier A, Vogt G, de Beaucoudrey L, Feinberg J, Jouanguy E, Boisson-Dupuis S, Fieschi C, Picard C, Casanova JL (2006) Inborn errors of IL-12/23- and IFN-gamma-mediated immunity: molecular, cellular, and clinical features. Semin Immunol 18:347–361

    Article  CAS  PubMed  Google Scholar 

  34. Fischer A, Le Deist F, Hacein-Bey-Abina S, Andre-Schmutz I, Basile Gde S, de Villartay JP, Cavazzana-Calvo M (2005) Severe combined immunodeficiency. A model disease for molecular immunology and therapy. Immunol Rev 203:98–109

    Article  CAS  PubMed  Google Scholar 

  35. Fisher RA (1918) The correlation between relatives on the supposition of Mendelian inheritance. Trans R Soc Edinb 52:399–433

    Google Scholar 

  36. Fortier A, Min-Oo G, Forbes J, Lam-Yuk-Tseung S, Gros P (2005) Single gene effects in mouse models of host: pathogen interactions. J Leukoc Biol 77:868–877

    Article  CAS  PubMed  Google Scholar 

  37. Gaspar HB, Parsley KL, Howe S, King D, Gilmour KC, Sinclair J, Brouns G, Schmidt M, Vo n Kalle C, Barington T, Jakobsen MA, Christensen HO, Al Ghonaium A, White HN, Smith JL, Levinsky RJ, Ali RR, Kinnon C, Thrasher AJ (2004) Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretrovi-ral vector. Lancet 364:2181–2187

    Article  CAS  PubMed  Google Scholar 

  38. Gatti RA, Meuwissen HJ, Allen HD, Hong R, Good RA (1968) Immunological reconstitution of sex-linked lym-phopenic immunological deficiency. Lancet 2:1366–1369

    Article  CAS  PubMed  Google Scholar 

  39. Glass WG, McDermott DH, Lim JK, Lekhong S, Yu SF, Frank WA, Pape J, Cheshier RC, Murphy PM (2006) CCR5 deficiency increases risk of symptomatic West Nile virus infection. J Exp Med 203:35–40

    Article  CAS  PubMed  Google Scholar 

  40. Good RA (1987) Bone marrow transplantation for immuno-deficiency diseases. Am J Med Sci 294:68–74

    Article  CAS  PubMed  Google Scholar 

  41. Greenwood CM, Fujiwara TM, Boothroyd LJ, Miller MA, Frappier D, Fanning EA, Schurr E, Morgan K (2000) Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family. Am J Hum Genet 67:405–416

    Article  CAS  PubMed  Google Scholar 

  42. Hacein-Bey-Abina S, Von Kalle C, Schmidt M, McCormack MP, Wulffraat N, Leboulch P, Lim A, Osborne CS, Pawliuk R, Morillon E, Sorensen R, Forster A, Fraser P, Cohen JI, de Saint Basile G, Alexander I, Wintergerst U, Frebourg T, Aurias A, Stoppa-Lyonnet D, Romana S, Radford-Weiss I, Gross F, Valensi F, Delabesse E, Macintyre E, Sigaux F, Soulier J, Leiva LE, Wissler M, Prinz C, Rabbitts TH, Le Deist F, Fischer A, Cavazzana-Calvo M (2003) LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1. Science 302:415–419

    Article  CAS  PubMed  Google Scholar 

  43. Howe SJ, Mansour MR, Schwarzwaelder K, Bartholomae C, Hubank M, Kempski H, Brugman MH, Pike-Overzet K, Chatters SJ, de Ridder D, Gilmour KC, Adams S, Thornhill SI, Parsley KL, Staal FJ, Gale RE, Linch DC, Bayford J, Brown L, Quaye M, Kinnon C, Ancliff P, Webb DK, Schmidt M, von Kalle C, Gaspar HB, Thrasher AJ (2008) Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients. J Clin Invest 118(9):3143–3150

    Article  CAS  PubMed  Google Scholar 

  44. Jouanguy E, Altare F, Lamhamedi S, Revy P, Emile JF, Newport M, Levin M, Blanche S, Seboun E, Fischer A, Casanova JL (1996) Interferon-gamma-receptor deficiency in an infant with fatal bacille Calmette-Guerin infection. N Engl J Med 335:1956–1961

    Article  CAS  PubMed  Google Scholar 

  45. Khoury MJ, Beaty TH, Cohen BH (1993) Fundamentals of genetic epidemiology. Oxford University Press, New York

    Google Scholar 

  46. Kwiatkowski D (2000) Science, medicine, and the future: susceptibility to infection. BMJ 321:1061–1065

    Article  CAS  PubMed  Google Scholar 

  47. Kwiatkowski DP (2005) How malaria has affected the human genome and what human genetics can teach us about malaria. Am J Hum Genet 77:171–192

    Article  CAS  PubMed  Google Scholar 

  48. Lalouel JM, Rao DC, Morton NE, Elston RC (1983) A uni-fied model for complex segregation analysis. Am J Hum Genet 35:816–826

    CAS  PubMed  Google Scholar 

  49. Le Pendu J, Ruvoen-Clouet N, Kindberg E, Svensson L (2006) Mendelian resistance to human norovirus infections. Semin Immunol 18:375–386

    Article  PubMed  CAS  Google Scholar 

  50. Lindesmith L, Moe C, Marionneau S, Ruvoen N, Jiang X, Lindblad L, Stewart P, LePendu J, Baric R (2003) Human susceptibility and resistance to Norwalk virus infection. Nat Med 9:548–553

    Article  CAS  PubMed  Google Scholar 

  51. Liu R, Paxton WA, Choe S, Ceradini D, Martin SR, Horuk R, MacDonald ME, Stuhlmann H, Koup RA, Landau NR (1996) Homozygous defects in HIV-1 coreceptor accounts for resistance of some multiply-exposed individuals to HIV-1 infection. Cell 86:367–377

    Article  CAS  PubMed  Google Scholar 

  52. Malik S, Abel L, Tooker H, Poon A, Simkin L, Girard M, Adams GJ, Starke JR, Smith KC, Graviss EA, Musser JM, Schurr E (2005) Alleles of the NRAMP1 gene are risk factors for pediatric tuberculosis disease. Proc Natl Acad Sci USA 102:12183–12188

    Article  CAS  PubMed  Google Scholar 

  53. Marionneau S, Ruvoen N, Le Moullac-Vaidye B, Clement M, Cailleau-Thomas A, Ruiz-Palacois G, Huang P, Jiang X, Le Pendu J (2002) Norwalk virus binds to histo-blood group antigens present on gastroduodenal epithelial cells of secre-tor individuals. Gastroenterology 122:1967–1977

    Article  CAS  PubMed  Google Scholar 

  54. Marquet S, Abel L, Hillaire D, Dessein H, Kalil J, Feingold J, Weissenbach J, Dessein AJ (1996) Genetic localization of a locus controlling the intensity of infection by Schistosoma mansoni on chromosome 5q31–q33. Nat Genet 14:181–184

    Article  CAS  PubMed  Google Scholar 

  55. Miller LH, Mason SJ, Clyde DF, McGinniss MH (1976) The resistance factor to Plasmodium vivax in blacks. The Duffy-blood-group genotype, FyFy. N Engl J Med 295:302–304

    CAS  PubMed  Google Scholar 

  56. Mira MT, Alcais A, Nguyen VT, Moraes MO, Di Flumeri C, Vu HT, Mai CP, Nguyen TH, Nguyen NB, Pham XK, Sarno EN, Alter A, Montpetit A, Moraes ME, Moraes JR, Dore C, Gallant CJ, Lepage P, Verner A, Van De Vosse E, Hudson TJ, Abel L, Schurr E (2004) Susceptibility to leprosy is associated with PARK2 and PACRG. Nature 427:636–640

    Article  CAS  PubMed  Google Scholar 

  57. Mira MT, Alcais A, Van Thuc N, Thai VH, Huong NT, Ba NN, Verner A, Hudson TJ, Abel L, Schurr E (2003) Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population. Nat Genet 33:412–415

    Article  CAS  PubMed  Google Scholar 

  58. Modiano D, Luoni G, Sirima BS, Simpore J, Verra F, Konate A, Rastrelli E, Olivieri A, Calissano C, Paganotti GM, D'Urbano L, Sanou I, Sawadogo A, Modiano G, Coluzzi M (2001) Haemoglobin C protects against clinical Plasmodium falciparum malaria. Nature 414:305–308

    Article  CAS  PubMed  Google Scholar 

  59. Newport MJ, Huxley CM, Huston S, Hawrylowicz CM, Oostra BA, Williamson R, Levin M (1996) A mutation in the interferon-gamma-receptor gene and susceptibility to mycobacterial infection. N Engl J Med 335:1941–1949

    Article  CAS  PubMed  Google Scholar 

  60. Nicolle C (1937) Destin des maladies infectieuses, 3rd edn. Alcan, Paris

    Google Scholar 

  61. Notarangelo L, Casanova JL, Conley ME, Chapel H, Fischer A, Puck J, Roifman C, Seger R, Geha RS (2006) Primary immunodeficiency diseases: an update from the International Union of Immunological Societies Primary Immunodeficiency Diseases Classification Committee Meeting in Budapest, 2005. J Allergy Clin Immunol 117:883–896

    Article  PubMed  Google Scholar 

  62. Novembre J, Galvani AP, Slatkin M (2005) The geographic spread of the CCR5 Delta32 HIV-resistance allele. PLoS Biol 3:e339

    Article  PubMed  CAS  Google Scholar 

  63. Ochs H, Smith CIE, Puck J (2006) Primary Immunodeficiencies: a molecular and genetic approach, 2nd edn. Oxford University Press, New York

    Google Scholar 

  64. Orth G (2006) Genetics of epidermodysplasia verruci-formis: insights into host defense against papillomaviruses. Semin Immunol 18:362–374

    Article  CAS  PubMed  Google Scholar 

  65. Pasteur L (1870) Etudes sur la maladie des vers a soie. La pébrine et la flacherie (tome I). Gauthier-Villars, Paris

    Google Scholar 

  66. Pasteur Vallery-Radot L (1939) Oeuvres complètes de Louis Pasteur, réunieset annotées par Pasteur Vallery-Radot. Masson et Cie, Paris

    Google Scholar 

  67. Picard C, Casanova JL, Abel L (2006) Mendelian traits that confer predisposition or resistance to specific infections in humans. Curr Opin Immunol 18:383–390

    Article  CAS  PubMed  Google Scholar 

  68. Picard C, Puel A, Bonnet M, Ku CL, Bustamante J, Yang K, Soudais C, Dupuis S, Feinberg J, Fieschi C, Elbim C, Hitchcock R, Lammas D, Davies G, Al-Ghonaium A, Al-Rayes H, Al-Jumaah S, Al-Hajjar S, Al-Mohsen IZ, Frayha HH, Rucker R, Hawn TR, Aderem A, Tufenkeji H, Haraguchi S, Day NK, Good RA, Gougerot-Pocidalo MA, Ozinsky A, Casanova JL (2003) Pyogenic bacterial infections in humans with IRAK-4 deficiency. Science 299:2076–2079

    Article  CAS  PubMed  Google Scholar 

  69. Pritchard JK (2001) Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 69:124–137

    Article  CAS  PubMed  Google Scholar 

  70. Purtilo DT, Cassel CK, Yang JP, Harper R (1975) X-linked recessive progressive combined variable immunodeficiency (Duncan's disease). Lancet 1:935–940

    Article  CAS  PubMed  Google Scholar 

  71. Quintana-Murci L, Alcais A, Abel L, Casanova JL (2007) Immunology in natura: clinical, epidemiological and evolutionary genetics of infectious diseases. Nat Immunol 8:1165–1171

    Article  CAS  PubMed  Google Scholar 

  72. Ramoz N, Rueda LA, Bouadjar B, Montoya LS, Orth G, Favre M (2002) Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis. Nat Genet 32:579–581

    Article  CAS  PubMed  Google Scholar 

  73. Rigaud S, Fondaneche MC, Lambert N, Pasquier B, Mateo V, Soulas P, Galicier L, Le Deist F, Rieux-Laucat F, Revy P, Fischer A, De Saint Basile G, Latour S (2006) XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome. Nature 444:110–114

    Article  CAS  PubMed  Google Scholar 

  74. Rioux JD, Xavier RJ, Taylor KD, Silverberg MS, Goyette P, Huett A, Green T, Kuballa P, Barmada MM, Datta LW, Shugart YY, Griffiths AM, Targan SR, Ippoliti AF, Bernard EJ, Mei L, Nicolae DL, Regueiro M, Schumm LP, Steinhart AH, Rotter JI, Duerr RH, Cho JH, Daly MJ, Brant SR (2007) Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. Nat Genet 39:596–604

    Article  CAS  PubMed  Google Scholar 

  75. Risch N (1990) Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Am J Hum Genet 46:242–253

    CAS  PubMed  Google Scholar 

  76. Risch N, Merikangas K (1996) The future of genetic studies of complex human diseases. Science 273:1516–1517

    Article  CAS  PubMed  Google Scholar 

  77. Sabeti PC, Walsh E, Schaffner SF, Varilly P, Fry B, Hutcheson HB, Cullen M, Mikkelsen TS, Roy J, Patterson N, Cooper R, Reich D, Altshuler D, O'Brien S, Lander ES (2005) The case for selection at CCR5-Delta32. PLoS Biol 3:e378

    Article  PubMed  CAS  Google Scholar 

  78. Samson M, Libert F, Doranz BJ, Rucker J, Liesnard C, Farber CM, Saragosti S, Lapoumeroulie C, Cognaux J, Forceille C, Muyldermans G, Verhofstede C, Burtonboy G, Georges M, Imai T, Rana S, Yi Y, Smyth RJ, Collman RG, Doms RW, Vassart G, Parmentier M (1996) Resistance to HIV-1 infection in caucasian individuals bearing mutant alleles of teh CCR5 chemokine receptor gene. Nature 382:722–725

    Article  CAS  PubMed  Google Scholar 

  79. Schurr E, Alcais A, de Leseleuc L, Abel L (2006) Genetic predisposition to leprosy: a major gene reveals novel pathways of immunity to Mycobacterium leprae. Semin Immunol 18:404–410

    Article  CAS  PubMed  Google Scholar 

  80. Siddiqui MR, Meisner S, Tosh K, Balakrishnan K, Ghei S, Fisher SE, Golding M, Shanker Narayan NP, Sitaraman T, Sengupta U, Pitchappan R, Hill AV (2001) A major suscep-tibility locus for leprosy in India maps to chromosome 10p13. Nat Genet 27:439–441

    Article  CAS  PubMed  Google Scholar 

  81. Sladek R, Rocheleau G, Rung J, Dina C, Shen L, Serre D, Boutin P, Vincent D, Belisle A, Hadjadj S, Balkau B, Heude B, Charpentier G, Hudson TJ, Montpetit A, Pshezhetsky AV, Prentki M, Posner BI, Balding DJ, Meyre D, Polychronakos C, Froguel P (2007) A genome-wide association study identifies novel risk loci for type 2 diabetes. Nature 445:881–885

    Article  CAS  PubMed  Google Scholar 

  82. Sorensen TI, Nielsen GG, Andersen PK, Teasdale TW (1988) Genetic and environmental influences on premature death in adult adoptees. N Engl J Med 318:727–732

    Article  CAS  PubMed  Google Scholar 

  83. Stephens JC, Reich DE, Goldstein DB, Shin HD, Smith MW, Carrington M, Winkler C, Huttley GA, Allikmets R, Schriml L, Gerrard B, Malasky M, Ramos MD, Morlot S, Tzetis M, Oddoux C, di Giovine FS, Nasioulas G, Chandler D, Aseev M, Hanson M, Kalaydjieva L, Glavac D, Gasparini P, Dean M et al (1998) Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplo-types. Am J Hum Genet 62:1507–1515

    Article  CAS  PubMed  Google Scholar 

  84. Thorven M, Grahn A, Hedlund KO, Johansson H, Wahlfrid C, Larson G, Svensson L (2005) A homozygous nonsense mutation (428G—>A) in the human secretor (FUT2) gene provides resistance to symptomatic norovirus (GGII) infections. J Virol 79:15351–15355

    Article  CAS  PubMed  Google Scholar 

  85. Tournamille C, Colin Y, Cartron JP, Le Van Kim C (1995) Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals. Nat Genet 10:224–228

    Article  CAS  PubMed  Google Scholar 

  86. Vanhollebeke B, Truc P, Poelvoorde P, Pays A, Joshi PP, Katti R, Jannin JG, Pays E (2006) Human Trypanosoma evansi infection linked to a lack of apolipoprotein L-I. N Engl J Med 355:2752–2756

    Article  CAS  PubMed  Google Scholar 

  87. Vogel F, Motulsky AG (1997) Human genetics: problems and approaches, 3 completely revth edn. Springer, Berlin

    Google Scholar 

  88. WHO (2006) Global leprosy situation, 2006. Wkly Epidemiol Rec 81:309–316

    Google Scholar 

  89. Zhang S Y, Jouanguy E, Ugolini S, Smahi A, Elain G, Romero P, Segal D, Sancho-Shimizu V, Lorenzo L, Puel A, Picard C, Chapgier A, Plancoulaine S, Titeux M, Cognet C, von Bernuth H, Ku CL, Casrouge A, Zhang XX, Barreiro L, Leonard J, Hamilton C, Lebon P, Heron B, Vallee L, Quintana-Murci L, Hovnanian A, Rozenberg F, Vivier E, Geissmann F, Tardieu M, Abel L, Casanova JL (2007) TLR3 deficiency in patients with herpes simplex encephalitis. Science 317:1522–1527

    Article  CAS  PubMed  Google Scholar 

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Laurent Abel, A.A., Casanova, JL. (2010). Human Genetics of Infectious Diseases. In: Speicher, M.R., Motulsky, A.G., Antonarakis, S.E. (eds) Vogel and Motulsky's Human Genetics. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-37654-5_14

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