Bellamy R J, Hill A V
Wellcome Trust Centre for Human Genetics, Oxford University, UK.
Novartis Found Symp. 1998;217:3-13; discussion 13-23. doi: 10.1002/0470846526.ch2.
Convincing evidence exists that host genes influence the outcome of infection in human tuberculosis. We are employing two complementary strategies to find the genes involved: a linkage-based, comprehensive genome screen and an association-based candidate gene study. In a genome screen of 282 markers on 92 affected sib pairs we have found evidence of co-segregation of disease with five markers, but further studies are required to replicate these results. The absence of a single strongly linked marker demonstrates that susceptibility to human tuberculosis is not controlled by a single major gene. Using a candidate gene approach investigating over 400 tuberculosis cases and 400 ethnically matched healthy controls we have found evidence that NR AMP1 and vitamin D receptor gene (VDR) polymorphisms are associated with tuberculosis. It is hoped that by identifying the genes that account for why only a minority of those exposed to tuberculosis develop disease, we will develop new insights into potential therapeutic and preventative strategies.
有确凿证据表明宿主基因会影响人类结核病感染的结果。我们正在采用两种互补策略来寻找相关基因:基于连锁分析的全基因组筛查和基于关联分析的候选基因研究。在对92对患病同胞对进行的282个标记的基因组筛查中,我们发现有5个标记与疾病共分离的证据,但需要进一步研究来重复这些结果。缺乏单一强连锁标记表明,人类结核病易感性不受单个主要基因控制。采用候选基因方法,对400多例结核病病例和400名种族匹配的健康对照进行研究,我们发现证据表明NRAMP1和维生素D受体基因(VDR)多态性与结核病有关。希望通过确定那些能解释为何仅有少数接触结核病的人发病的基因,我们能对潜在的治疗和预防策略有新的认识。