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树突状细胞衍生的外泌体对初始CD4+ T细胞的间接激活。

Indirect activation of naïve CD4+ T cells by dendritic cell-derived exosomes.

作者信息

Théry Clotilde, Duban Livine, Segura Elodie, Véron Philippe, Lantz Olivier, Amigorena Sebastian

机构信息

INSERM U520, Institut Curie, 12 rue Lhomond, 75005 Paris, France.

出版信息

Nat Immunol. 2002 Dec;3(12):1156-62. doi: 10.1038/ni854. Epub 2002 Nov 11.

Abstract

Dendritic cells (DCs) secrete vesicles of endosomal origin, called exosomes, that bear major histocompatibility complex (MHC) and T cell costimulatory molecules. Here, we found that injection of antigen- or peptide-bearing exosomes induced antigen-specific naïve CD4+ T cell activation in vivo. In vitro, exosomes did not induce antigen-dependent T cell stimulation unless mature CD8alpha- DCs were also present in the cultures. These mature DCs could be MHC class II-negative, but had to bear CD80 and CD86. Therefore, in addition to carrying antigen, exosomes promote the exchange of functional peptide-MHC complexes between DCs. Such a mechanism may increase the number of DCs bearing a particular peptide, thus amplifying the initiation of primary adaptive immune responses.

摘要

树突状细胞(DCs)分泌源自内体的囊泡,称为外泌体,其携带主要组织相容性复合体(MHC)和T细胞共刺激分子。在此,我们发现注射携带抗原或肽的外泌体可在体内诱导抗原特异性初始CD4 + T细胞活化。在体外,外泌体不会诱导抗原依赖性T细胞刺激,除非培养物中也存在成熟的CD8α-DCs。这些成熟的DCs可能为II类MHC阴性,但必须携带CD80和CD86。因此,外泌体除了携带抗原外,还促进DCs之间功能性肽-MHC复合物的交换。这种机制可能会增加携带特定肽的DCs数量,从而放大初次适应性免疫反应的启动。

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