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Naturally Arising Human CD4 T-Cells That Recognize Islet Autoantigens and Secrete Interleukin-10 Regulate Proinflammatory T-Cell Responses via Linked Suppression

机译:自然产生识别胰岛自身抗原并分泌白介素10的人类CD4 T细胞通过链接抑制调节促炎性T细胞反应。

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摘要

OBJECTIVERegulatory T-cells (Tregs) recognizing islet autoantigens are proposed as a key mechanism in the maintenance of self-tolerance and protection from type 1 diabetes. To date, however, detailed information on such cells in humans, and insight into their mechanisms of action, has been lacking. We previously reported that a subset of CD4 T-cells secreting high levels of the immunosuppressive cytokine interleukin-10 (IL-10) is significantly associated with late onset of type 1 diabetes and is constitutively present in a majority of nondiabetic individuals. Here, we test the hypothesis that these T-cells represent a naturally generated population of Tregs capable of suppressing proinflammatory T-cell responses.
机译:目的提出识别胰岛自身抗原的调节性T细胞(Tregs)是维持自我耐受和预防1型糖尿病的关键机制。然而,迄今为止,还缺乏关于人类中此类细胞的详细信息以及对它们的作用机理的深入了解。我们以前曾报道过,分泌高水平的免疫抑制细胞因子白介素10(IL-10)的CD4 T细胞子集与1型糖尿病的晚期发作显着相关,并且在大多数非糖尿病个体中组成性存在。在这里,我们测试了以下假设:这些T细胞代表能够抑制促炎性T细胞反应的自然产生的Treg群体。

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