Cutting Edge: Limited Specialization of Dendritic Cell Subsets for MHC Class II-Associated Presentation of Viral Particles

被引:42
作者
Keller, Susanne A. [1 ]
Bauer, Monika [1 ]
Manolova, Vania [1 ]
Muntwiler, Simone [1 ]
Saudan, Philippe [1 ]
Bachmann, Martin F. [1 ]
机构
[1] Cytos Biotechnol AG, CH-8952 Zurich, Switzerland
关键词
VIRUS-LIKE PARTICLES; CYTOTOXIC T-CELLS; IN-VIVO; ANTIGEN PRESENTATION; CROSS-PRESENTATION; CD8; EXPRESSION; MOUSE THYMUS; SPLEEN; ACTIVATION; RESPONSES;
D O I
10.4049/jimmunol.0901540
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) are the most important APC. It was recently reported that there is a dichotomy for Ag presentation by DC subsets; exogenous Ags reach the MHC class I pathway, but not the MHC class II pathway, in CD8(+) DCs, whereas CD8(-) DCs only process Ags for the MHC class II pathway. In this study, we used virus-like particles (VLPs) to show that CD8(+) and CD8(-) DCs efficiently capture and process VLPs for presentation in association with MHC class II in vivo. In contrast, CD8(+) DCs, but not CD8(-) DCs, cross presented VIP-derived peptides. This pattern was changed in an Fc gamma R-dependent fashion in the presence of VLP-specific Abs, because under those conditions both DC subsets failed to efficiently cross present. Thus, the presentation of viral particles to CD4(+) T cells is not restricted to distinct DC subsets, whereas the presentation of viral particles to CD8(+) T cells is limited to CD8(+) DCs. The Journal of Immunology, 2010, 184: 26-29.
引用
收藏
页码:26 / 29
页数:4
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