Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Bahia, Brazil; Faculdade de Medicina, Universidade Federal da Bahia, Salvador, Bahia, Brazil; Multinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Fundação José Silveira, Salvador, Bahia, Brazil.
Laboratório de Micobacteriologia Molecular, Centro de Pesquisas em Doenças Infecciosas e Parasitárias- CEPEDIP - Universidade Federal do Rio de Janeiro, Rio de janeiro, Brazil; Programa Acadêmico de Tuberculose, Faculdade de Medicina e Complexo Hospitalar HUCFF-IDT, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Int J Infect Dis. 2020 Mar;92:21-28. doi: 10.1016/j.ijid.2019.12.013. Epub 2019 Dec 13.
Host genetic polymorphisms may be important in determining susceptibility to Mycobacterium tuberculosis (Mtb) infection, but their role is not fully understood. Detection of microbial DNA and activation of type I interferon (IFN) pathways regulate macrophage responses to Mtb infection.
We examined whether seven candidate gene SNPs were associated with tuberculin skin test (TST) positivity in close contacts of microbiologically confirmed pulmonary TB patients in Brazil. Independent associations with TST positivity were tested using multivariable logistic regression (using genotypes and clinical variables) and genetic models.
Among 482 contacts of 145 TB index cases, 296 contacts were TST positive. Multivariable regression analysis adjusted for population admixture, age, family relatedness, sex and clinical variables related to increased TB risk demonstrated that SNPs in PYHIN1-IFI16-AIM2 rs1101998 (adjusted OR [aOR]: 3.72; 95%CI=1.15-12.0; p=0.028) and in PYHIN1-IFI16-AIM2 rs1633256 (aOR=24.84; 95%CI=2.26-272.95; p=0.009) were associated with TST positivity in a recessive model. Furthermore, an IRF7 polymorphism (rs11246213) was associated with reduced odds of TST positivity in a dominant model (aOR: 0.50, 95%CI: 0.26-0.93; p=0.029).
Polymorphisms in PYHIN1-IFI16-AIM2 rs1633256, rs1101998 and in IRF7 rs11246213 were associated with altered susceptibility to Mtb infection in this Brazilian cohort.
宿主遗传多态性可能在决定对结核分枝杆菌(Mtb)感染的易感性方面起重要作用,但它们的作用尚未完全阐明。微生物 DNA 的检测和 I 型干扰素(IFN)途径的激活调节巨噬细胞对 Mtb 感染的反应。
我们研究了巴西经微生物学证实的肺结核患者的密切接触者中,七个候选基因 SNP 是否与结核菌素皮肤试验(TST)阳性相关。使用多变量逻辑回归(使用基因型和临床变量)和遗传模型测试 TST 阳性的独立相关性。
在 145 例结核指数病例的 482 名接触者中,有 296 名接触者 TST 阳性。多变量回归分析调整了人群混合、年龄、家族关系、性别和与增加结核病风险相关的临床变量,表明 PYHIN1-IFI16-AIM2 rs1101998(调整后的 OR [aOR]:3.72;95%CI=1.15-12.0;p=0.028)和 PYHIN1-IFI16-AIM2 rs1633256(aOR=24.84;95%CI=2.26-272.95;p=0.009)中的 SNP 与隐性模型中的 TST 阳性相关。此外,IRF7 多态性(rs11246213)与 TST 阳性的几率降低相关,呈显性模型(aOR:0.50,95%CI:0.26-0.93;p=0.029)。
在巴西队列中,PYHIN1-IFI16-AIM2 rs1633256、rs1101998 和 IRF7 rs11246213 的多态性与 Mtb 感染易感性改变相关。