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Plasmacytoid Dendritic Cells Take Up Opsonized Antigen Leading to CD4+ and CD8+ T Cell Activation In Vivo

机译:浆细胞样树突状细胞吸收调理素导致体内CD4 +和CD8 + T细胞活化

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摘要

Plasmacytoid dendritic cells (pDC) are the body’s main source of IFN-α, but, unlike classical myeloid DC (myDC), they lack phagocytic activity and are generally perceived as playing only a minor role in Ag processing and presentation. We show that murine pDC, as well as myDC, express Fcγ receptors (CD16/CD32) and can use these receptors to acquire Ag from immune complexes (IC), resulting in the induction of robust Ag-specific CD4+ and CD8+ T cell responses. IC-loaded pDC stimulate CD4 + T cells to proliferate and secrete a mixture of IL-4 and IFN-γ, and they induce CD8+ T cells to secrete IL-10 as well as IFN-γ. In contrast, IC-loaded myDC induce both CD4+ and CD8+ T cells to secrete mainly IFN-γ. These results indicate that pDC can shape an immune response by acquiring and processing opsonized Ag, leading to a predominantly Th2 response.
机译:浆细胞样树突状细胞(pDC)是人体中IFN-α的主要来源,但与传统的髓样DC(myDC)不同,它们缺乏吞噬功能,通常被认为在Ag的加工和呈递中仅起次要作用。我们证明,鼠pDC以及myDC均表达Fcγ受体(CD16 / CD32),并可以利用这些受体从免疫复合物(IC)中获得Ag,从而诱导出健壮的Ag特异性CD4 + 和CD8 + T细胞反应。负载IC的pDC刺激CD4 + T细胞增殖并分泌IL-4和IFN-γ的混合物,它们诱导CD8 + T细胞分泌IL-10。以及IFN-γ。相反,负载IC的myDC诱导CD4 + 和CD8 + T细胞主要分泌IFN-γ。这些结果表明,pDC可以通过获取和处理调理过的Ag来塑造免疫应答,从而导致Th2应答。

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