生物
增强子
遗传学
基因
自身免疫
T细胞
免疫系统
人口
人类白细胞抗原
基因表达
免疫学
抗原
医学
环境卫生
作者
Chun Ye,Ting Feng,Ho‐Keun Kwon,Towfique Raj,Michael T. Wilson,Natasha Asinovski,Cristin McCabe,Michelle Lee,Irene Y. Frohlich,Hyun-il Paik,Noah Zaitlen,Nir Hacohen,Barbara E. Stranger,Philip L. De Jager,Diane Mathis,Aviv Regev,Christophe Benoist
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2014-09-11
卷期号:345 (6202)
被引量:249
标识
DOI:10.1126/science.1254665
摘要
T lymphocyte activation by antigen conditions adaptive immune responses and immunopathologies, but we know little about its variation in humans and its genetic or environmental roots. We analyzed gene expression in CD4(+) T cells during unbiased activation or in T helper 17 (T(H)17) conditions from 348 healthy participants representing European, Asian, and African ancestries. We observed interindividual variability, most marked for cytokine transcripts, with clear biases on the basis of ancestry, and following patterns more complex than simple T(H)1/2/17 partitions. We identified 39 genetic loci specifically associated in cis with activated gene expression. We further fine-mapped and validated a single-base variant that modulates YY1 binding and the activity of an enhancer element controlling the autoimmune-associated IL2RA gene, affecting its activity in activated but not regulatory T cells. Thus, interindividual variability affects the fundamental immunologic process of T helper activation, with important connections to autoimmune disease.
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