Mendelian and complex genetics of susceptibility and resistance to parasitic infections

被引:43
作者
Campino, Susana
Kwiatkowski, Dominic
Dessein, Alain
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[2] Univ Mediterranee, Fac Med, INSERM,UMR 399, Unit Genet & Immunol Parasit Dis, Marseille, France
基金
英国医学研究理事会;
关键词
parasitic infections; malaria; schistosomiasis; leishmaniasis; genetics;
D O I
10.1016/j.smim.2006.07.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Uncovering the complex genetic basis of susceptibility and resistance to parasitic infectious diseases is an enormous challenge. It probably involves many different host genes, interacting with multiple parasite genetic and environmental factors. Several genes of interest have been identified by family and association studies in humans and by using mouse models, but more robust epidemiological studies and functional data are needed to authenticate these findings. With new technologies and statistical tools for whole-genome association analysis, the next few years are likely to see acceleration in the rate of gene discovery, which has the potential to greatly assist drug and vaccine development. (C) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:411 / 422
页数:12
相关论文
共 136 条
[1]  
ABAZA H, 1985, TISSUE ANTIGENS, V26, P307, DOI 10.1111/j.1399-0039.1985.tb02228.x
[2]  
ABDELSALAM E, 1986, TISSUE ANTIGENS, V27, P142, DOI 10.1111/j.1399-0039.1986.tb01513.x
[3]  
ABEL L, 1992, AM J HUM GENET, V50, P1308
[4]  
ABEL L, 1991, AM J HUM GENET, V48, P959
[5]   A comparison of case-control and family-based association methods: The example of sickle-cell and malaria [J].
Ackerman, H ;
Usen, S ;
Jallow, M ;
Sisay-Joof, F ;
Pinder, M ;
Kwiatkowski, DP .
ANNALS OF HUMAN GENETICS, 2005, 69 :559-565
[6]   Complex haplotypic structure of the central MHC region flanking TNF in a West African population [J].
Ackerman, HC ;
Ribas, G ;
Jallow, M ;
Mott, R ;
Neville, M ;
Sisay-Joof, F ;
Pinder, M ;
Campbell, RD ;
Kwiatkowski, DP .
GENES AND IMMUNITY, 2003, 4 (07) :476-486
[7]   Hemoglobin C associated with protection from severe malaria in the Dogon of Mali, a West African population with a low prevalence of hemoglobin S [J].
Agarwal, A ;
Guindo, A ;
Cissoko, Y ;
Taylor, JG ;
Coulibaly, D ;
Koné, A ;
Kayentao, K ;
Djimde, A ;
Plowe, CV ;
Doumbo, O ;
Wellems, TE ;
Diallo, D .
BLOOD, 2000, 96 (07) :2358-2363
[8]   Protective effects of the sickle cell gene against malaria morbidity and mortality [J].
Aidoo, M ;
Terlouw, DJ ;
Kolczak, M ;
McElroy, PD ;
ter Kuile, FO ;
Kariuki, S ;
Nahlen, BL ;
Lal, AA ;
Udhayakumar, V .
LANCET, 2002, 359 (9314) :1311-1312
[9]   Tumor necrosis factor-α promoter variant 2 (TNF2) is associated with pre-term delivery, infant mortality, and malaria morbidity in western Kenya:: Asenibo Bay Cohort project IX [J].
Aidoo, M ;
Mcelroy, PD ;
Kolczak, MS ;
Terlouw, DJ ;
ter Kuile, FO ;
Nahlen, B ;
Lal, AA ;
Udhayakumar, V .
GENETIC EPIDEMIOLOGY, 2001, 21 (03) :201-211
[10]   Population genetics -: Malaria susceptibility and CD36 mutation [J].
Aitman, TJ ;
Cooper, LD ;
Norsworthy, PJ ;
Wahid, FN ;
Gray, JK ;
Curtis, BR ;
McKeigue, PM ;
Kwiatkowski, D ;
Greenwood, BM ;
Snow, RW ;
Hill, AV ;
Scott, J .
NATURE, 2000, 405 (6790) :1015-1016