Laboratory of Medical Investigation in Dermatology and Immunodeficiency, LIM-56, Faculty of Medicine, University of Sao Paulo, Sao Paulo, Brazil.
J Acquir Immune Defic Syndr. 2013 Jun 1;63(2):147-51. doi: 10.1097/QAI.0b013e31828f93bb.
HLA and other genetic variants, playing an important role in innate and adaptive immunity, are known to influence tuberculosis (TB) development in HIV-1-positive (HIV+) patients. Because inflammasome genes contribute to HIV-1 susceptibility, we investigated the possible association between polymorphisms in inflammasome genes with HIV-1 and Mycobacterium tuberculosis coinfection (HIV+TB+) in a case/control cohort of Brazilian individuals. Nineteen single-nucleotide polymoprhims in 8 inflammasome genes (NLRP1, NLRP3, AIM2, CARD8, CASP1, IL1B, IL1R, and HSP90) were analyzed in HIV+TB+ Brazilian patients (from Recife, Pernambuco). CARD8 rs6509365 polymorphism was associated with HIV+TB+ (P = 5 × 10(-5)), suggesting a predisposing role of this variant in M. tuberculosis susceptibility in HIV+ subjects (odds ratio = 2.45). This effect is even strong when this allele is combined to CARD8 rs2043211 single-nucleotide polymoprhim. The results of this study support the novel association between CARD8 gene and HIV+TB+ coinfection, demonstrating that inflammasome genetics could influence HIV-1 infection and the development of opportunistic infection.
HLA 和其他遗传变异体在先天和适应性免疫中起着重要作用,已知它们会影响 HIV-1 阳性(HIV+)患者的结核病(TB)发展。由于炎症小体基因有助于 HIV-1 的易感性,我们研究了炎症小体基因中的多态性与 HIV-1 和结核分枝杆菌合并感染(HIV+TB+)在巴西个体病例对照队列中的可能关联。在来自伯南布哥州累西腓的 HIV+TB+巴西患者中,分析了 8 个炎症小体基因(NLRP1、NLRP3、AIM2、CARD8、CASP1、IL1B、IL1R 和 HSP90)中的 19 个单核苷酸多态性。CARD8 rs6509365 多态性与 HIV+TB+相关(P = 5 × 10(-5)),表明该变体在 HIV+个体中对结核分枝杆菌易感性具有易感性作用(比值比= 2.45)。当该等位基因与 CARD8 rs2043211 单核苷酸多态性结合时,这种作用甚至更强。这项研究的结果支持 CARD8 基因与 HIV+TB+合并感染之间的新关联,表明炎症小体遗传学可能影响 HIV-1 感染和机会性感染的发展。