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Intersection of population variation and autoimmunity genetics in human T cell activation
Intersection of population variation and autoimmunity genetics in human T cell activation
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Intersection of population variation and autoimmunity genetics in human T cell activation
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Intersection of population variation and autoimmunity genetics in human T cell activation
Intersection of population variation and autoimmunity genetics in human T cell activation

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Intersection of population variation and autoimmunity genetics in human T cell activation
Intersection of population variation and autoimmunity genetics in human T cell activation
Journal Article

Intersection of population variation and autoimmunity genetics in human T cell activation

2014
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Overview
T cells are important in mounting immune responses to a host of pathogens, and they have also been implicated in autoimmune disease. By examining the variability in gene expression in stimulated T cells over time from a multi-ethnic cohort of healthy humans, Ye et al. identified specific genetic polymorphisms that explain differences among individuals in response to pathogens. Furthermore, a candidate gene approach led to the identification of a single-nucleotide polymorphism that controls the response of the autoimmune-associated IL2RA gene. This study helps us understand the degree to which immune responses are driven by the environment or by an individual's physiological or genetic factors. Science , this issue 10.1126/science.1254665 Profiles of T cell responses display genetically influenced interindividual variation. 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.