交叉展示
抗原呈递
CD8型
抗原
抗原提呈细胞
背景(考古学)
树突状细胞
免疫学
CD11c公司
主要组织相容性复合体
生物
趋化因子受体
趋化因子
细胞生物学
T细胞
MHC I级
免疫系统
表型
遗传学
基因
古生物学
作者
Annabell Bachem,Steffen Güttler,Evelyn Hartung,Frédéric Ebstein,Michael Schaefer,Astrid Tannert,Abdulgabar Salama,Kamran Movassaghi,Corinna Opitz,Hans W. Mages,V. Henn,Peter‐Michael Kloetzel,Stephanie Gurka,Richard A. Kroczek
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.
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