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Variants of the CD40 ligand gene are not associated with increased susceptibility to tuberculosis in West Africa
Authors:Campbell Sarah J  Sabeti Pardis  Fielding Katherine  Sillah Jackson  Bah Boubacar  Gustafson Per  Manneh Kebba  Lisse Ida  Sirugo Giorgio  Bellamy Richard  Bennett Steve  Aaby Peter  McAdam Keith P W J  Bah-Sow Oumou  Lienhardt Christian  Hill Adrian V S
Affiliation:(1) The Henry Wellcome Building of Genomic Medicine, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, OX3 7BN, UK;(2) London School of Hygiene and Tropical Medicine, Keppel Street, London, WC1E 7HT, UK;(3) Medical Research Council Laboratories, Fajara, The Gambia;(4) Programme National de Lutte Anti-Tuberculeuse, BP 634, Conakry, République de Guinée;(5) Projecto de Saude Bandim, Danish Epidemiology Service Centre, Statens Serum Institut, Bissau, Guinea-Bissau;(6) National TB/Leprosy Control Programme, Banjul, The Gambia;(7) Present address: I.R.D, Route des Peres Maristes, Hann, BP1386, Dakar, Senegal
Abstract: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, 3prime and 5prime regulatory sequences of the gene. Six single nucleotide polymorphisms (SNPs) and a 3prime 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.Sadly, Professor Steve Bennett passed away in March 2003
Keywords:Tuberculosis  Genetic susceptibility  Polymorphism  CD40 ligand
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