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Superior antigen cross-presentation and XCR1 expression define human CD11c+CD141+ cells as homologues of mouse CD8+ dendritic cells

机译:优异的抗原交叉呈递和XCR1表达将人CD11c + CD141 +细胞定义为小鼠CD8 +树突状细胞的同源物

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摘要

In recent years, human dendritic cells (DCs) could be subdivided into CD304+ plasmacytoid DCs (pDCs) and conventional DCs (cDCs), the latter encompassing the CD1c+, CD16+, and CD141+ DC subsets. To date, the low frequency of these DCs in human blood has essentially prevented functional studies defining their specific contribution to antigen presentation. We have established a protocol for an effective isolation of pDC and cDC subsets to high purity. Using this approach, we show that CD141+ DCs are the only cells in human blood that express the chemokine receptor XCR1 and respond to the specific ligand XCL1 by Ca2+ mobilization and potent chemotaxis. More importantly, we demonstrate that CD141+ DCs excel in cross-presentation of soluble or cell-associated antigen to CD8+ T cells when directly compared with CD1c+ DCs, CD16+ DCs, and pDCs from the same donors. Both in their functional XCR1 expression and their effective processing and presentation of exogenous antigen in the context of major histocompatibility complex class I, human CD141+ DCs correspond to mouse CD8+ DCs, a subset known for superior antigen cross-presentation in vivo. These data define CD141+ DCs as professional antigen cross-presenting DCs in the human.
机译:近年来,人树突状细胞(DC)可以细分为CD304 +浆细胞样DC(pDC)和常规DC(cDC),后者包括CD1c +,CD16 +和CD141 + DC子集。迄今为止,这些DC在人血中的频率很低,基本上阻止了功能研究定义其对抗原呈递的特定作用。我们已经建立了一个协议,可以有效地将pDC和cDC子集隔离到高纯度。使用这种方法,我们表明CD141 + DCs是人类血液中唯一表达趋化因子受体XCR1并通过Ca2 +动员和强趋化性对特异性配体XCL1作出反应的细胞。更重要的是,我们证明与直接来自同一供体的CD1c + DC,CD16 + DC和pDC相比,CD141 + DC在将可溶性或与细胞相关的抗原交叉呈递到CD8 + T细胞方面表现出色。在主要组织相容性复合体I类的功能XCR1表达以及有效处理和呈递外源抗原方面,人CD141 + DC均与小鼠CD8 + DC相对应,后者以体内优异的抗原交叉呈递而闻名。这些数据将CD141 + DC定义为人类中专业的抗原交叉呈递DC。

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