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

机译:人类T细胞活化中的种群变异与自身免疫遗传学的交集

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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.
机译:抗原激活T淋巴细胞可调节适应性免疫反应和免疫病理学,但我们对其在人体内的变异及其遗传或环境根源知之甚少。我们分析了来自欧洲,亚洲和非洲祖先的348位健康参与者的CD4(+)T细胞在无偏激活或T辅助17(T(H)17)条件下的基因表达。我们观察到个体间差异,其中最明显的是细胞因子转录本,根据血统有明显的偏倚,并且遵循的模式比简单的T(H)1/2/17划分更为复杂。我们确定了39个遗传基因座,具体与激活的基因表达顺式相关。我们进一步精细映射并验证了一个单碱基变异体,该变异体可调控YY1结合和控制自身免疫相关IL2RA基因的增强子元件的活性,从而影响其在活化的但不是调节性T细胞中的活性。因此,个体间的变异性会影响T辅助细胞活化的基本免疫过程,并与自身免疫性疾病具有重要联系。

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  • 来源
    《Science》 |2014年第6202期|1311-1311|共1页
  • 作者单位

    Broad Inst MIT & Harvard, Cambridge, MA 02142 USA;

    Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA;

    Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA;

    Broad Inst MIT & Harvard, Cambridge, MA 02142 USA|Brigham & Womens Hosp, Dept Neurol, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA|Brigham & Womens Hosp, Dept Psychiat, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA;

    Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA;

    Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA;

    Broad Inst MIT & Harvard, Cambridge, MA 02142 USA|Brigham & Womens Hosp, Dept Neurol, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA|Brigham & Womens Hosp, Dept Psychiat, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA;

    Brigham & Womens Hosp, Dept Neurol, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA|Brigham & Womens Hosp, Dept Psychiat, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA;

    Brigham & Womens Hosp, Dept Neurol, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA|Brigham & Womens Hosp, Dept Psychiat, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA;

    Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA;

    Univ Calif San Francisco, Lung Biol Ctr, Dept Med, San Francisco, CA 94158 USA;

    Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA;

    Univ Chicago, Med Genet Sect, Chicago, IL 60637 USA;

    Broad Inst MIT & Harvard, Cambridge, MA 02142 USA|Brigham & Womens Hosp, Dept Neurol, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA|Brigham & Womens Hosp, Dept Psychiat, Inst Neurosci, Program Translat NeuroPsychiat Genom, Boston, MA 02115 USA;

    Broad Inst MIT & Harvard, Cambridge, MA 02142 USA|Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA;

    Broad Inst MIT & Harvard, Cambridge, MA 02142 USA|MIT, Dept Biol, Howard Hughes Med Inst, Cambridge, MA 02139 USA;

    Broad Inst MIT & Harvard, Cambridge, MA 02142 USA|Harvard Univ, Sch Med, Dept Microbiol & Immunobiol, Div Immunol, Boston, MA 02115 USA;

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