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Genetic and Shared Environmental Influences on Interferon-γ Production in Response to Mycobacterium tuberculosis Antigens in a Ugandan Population

机译:遗传和共有的环境影响对乌干达人群中结核分枝杆菌抗原的干扰素-γ产生。

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摘要

Interferon-γ (IFN-γ) is a key cytokine in the immune response to Mycobacterium tuberculosis (Mtb). Many studies established IFN-γ responses are influenced by host genetics, however differed widely by the study design and heritability estimation method. We estimated heritability of IFN-γ responses to Mtb culture filtrate (CF), ESAT-6, and Antigen 85B (Ag85B) in 1,104 Ugandans from a household contact study. Our method separately evaluates shared environmental and genetic variance, therefore heritability estimates were not upwardly biased, ranging from 11.6% for Ag85B to 22.9% for CF. Subset analyses of individuals with latent Mtb infection or without human immunodeficiency virus infection yielded higher heritability estimates, suggesting 10–30% of variation in IFN-γ is caused by a shared environment. Immunosuppression does not negate the role of genetics on IFN-γ response. These estimates are remarkably close to those reported for components of the innate immune response. These findings have implications for the interpretation of IFN-γ response assays and vaccine studies.
机译:干扰素-γ(IFN-γ)是结核分枝杆菌(Mtb)免疫反应中的关键细胞因子。建立IFN-γ应答的许多研究受到宿主遗传学的影响,但是研究设计和遗传力估计方法差异很大。我们通过一项家庭接触研究估算了1,104名乌干达人对Mtb培养滤液(CF),ESAT-6和抗原85B(Ag85B)的IFN-γ反应的遗传力。我们的方法分别评估共享的环境和遗传方差,因此遗传率估计值没有偏倚,从Ag85B的11.6%到CF的22.9%不等。对具有潜在Mtb感染或没有人类免疫缺陷病毒感染的个体进行的子集分析得出了更高的遗传力估计值,表明IFN-γ变异的10%至30%是由共同的环境引起的。免疫抑制并不能消除遗传学对IFN-γ反应的作用。这些估计非常接近先天免疫应答成分的报道。这些发现对IFN-γ应答测定和疫苗研究的解释具有启示意义。

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