| Literature DB >> 25214635 |
Chun Jimmie Ye1, Ting Feng2, Ho-Keun Kwon2, Towfique Raj3, Michael T Wilson2, Natasha Asinovski2, Cristin McCabe3, Michelle H Lee4, Irene Frohlich4, Hyun-il Paik2, Noah Zaitlen5, Nir Hacohen2, Barbara Stranger6, Philip De Jager3, Diane Mathis7, Aviv Regev8, Christophe Benoist9.
Abstract
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.Entities:
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Year: 2014 PMID: 25214635 PMCID: PMC4751028 DOI: 10.1126/science.1254665
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728