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Immunomodulatory functions of BTLA and HVEM govern induction of extrathymic regulatory T cells and tolerance by dendritic cells

机译:BTLA和HVEM的免疫调节功能控制胸腺外调节性T细胞的诱导和树突状细胞的耐受性

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摘要

Dendritic cells (DCs) initiate immunity and also antigen-specific tolerance mediated by extrathymic regulatory T (Treg) cells. Yet it remains unclear how DCs regulate induction of such tolerance. Here we report that efficient induction of Treg cells was instructed by BTLA+DEC205+CD8+CD11c+ DCs and the immunomodulatory functions of BTLA. In contrast, T cell activation in steady state by total CD11c+ DCs that include a majority of DCs that do not express BTLA did not induce Treg cells and had no lasting impact on subsequent immune responses. Engagement of HVEM, a receptor of BTLA, promoted Foxp3 expression in T cells through upregulation of CD5. In contrast, T cells activated in the absence of BTLA and HVEM-mediated functions remained CD5lo and therefore failed to resist the inhibition of Foxp3 expression in response to effector cell-differentiating cytokines. Thus DCs require BTLA and CD5-dependent mechanisms to actively adjust tolerizing T cell responses under steady state conditions.
机译:树突状细胞(DC)启动免疫,并通过胸腺外调节性T(Treg)细胞介导抗原特异性耐受。然而,尚不清楚DC如何调节这种耐受性的诱导。在这里我们报告说,BTLA + DEC205 + CD8 + CD11c + DC和BTLA的免疫调节功能。相比之下,稳态的T细胞活化由总的CD11c + DC组成,其中包括大多数不表达BTLA的DC不会诱导Treg细胞,并且对随后的免疫反应没有持久的影响。参与BTLA受体的HVEM的参与通过上调CD5促进T细胞中Foxp3的表达。相反,在没有BTLA和HVEM介导的功能的情况下被激活的T细胞仍然是CD5 lo ,因此无法抵抗对效应细胞分化的细胞因子的Foxp3表达的抑制。因此,DC需要BTLA和CD5依赖性机制来在稳态条件下主动调节耐受性T细胞应答。

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