Variants of the CD40 ligand gene are not associated with increased susceptibility to tuberculosis in West Africa

被引:13
作者
Campbell, SJ
Sabeti, P
Fielding, K
Sillah, J
Bah, B
Gustafson, P
Manneh, K
Lisse, I
Sirugo, G
Bellamy, R
Bennett, S
Aaby, P
McAdam, KPWJ
Bah-Sow, O
Lienhardt, C
Hill, AVS
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England
[2] Univ London London Sch Hyg & Trop Med, London WC1E 7HT, England
[3] MRC Labs, Fajara, Gambia
[4] Programme Natl Lutte Anti TB, Conakry, Guinea
[5] Statens Serum Inst, Danish Epidemiol Serv Ctr, Projecto Saude Bandim, Bissau, Guinea Bissau
[6] Natl TB Leprosy Control Programme, Banjul, Gambia
基金
英国惠康基金;
关键词
tuberculosis; genetic susceptibility; polymorphism; CD40; ligand;
D O I
10.1007/s00251-003-0602-9
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Evidence for linkage between tuberculosis and human chromosomal region Xq26 has previously been described. The costimulatory molecule CD40 ligand, encoded by TNFSF5 and located at Xq26.3, is a promising positional candidate. Interactions between CD40 ligand and CD40 are involved in the development of humoral- and cell-mediated immunity, as well as the activation of macrophages, which are the primary host and effector cells for Mycobacterium tuberculosis. We hypothesised that common variation within TNFSF5 might affect susceptibility to tuberculosis disease and, thus, might be responsible for the observed linkage to Xq26. Sequencing 32 chromosomes from a Gambian population identified nine common polymorphisms within the coding, 3' and 5' regulatory sequences of the gene. Six single nucleotide polymorphisms (SNPs) and a 3' microsatellite were genotyped in 121 tuberculosis patients and their available parents. No association with tuberculosis was detected for these variants using a transmission disequilibrium test, although one SNP at -726 showed some evidence of association in males. This finding, however, did not replicate in a separate case control study of over 1,200 West African individuals. We conclude that common genetic variation in TNFSF5 is not likely to affect tuberculosis susceptibility in West Africa and the linkage observed in this region is not due to variation in TNFSF5.
引用
收藏
页码:502 / 507
页数:6
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