Distinct dendritic cell populations sequentially present antigen to CD4 T cells and stimulate different aspects of cell-mediated immunity

被引:584
作者
Itano, AA [1 ]
McSorley, SJ
Reinhardt, RL
Ehst, BD
Ingulli, E
Rudensky, AY
Jenkins, MK
机构
[1] Univ Minnesota, Sch Med, Dept Microbiol, Ctr Immunol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Sch Med, Dept Pediat, Ctr Immunol, Minneapolis, MN 55455 USA
[3] Univ Washington, Howard Hughes Med Inst, Dept Immunol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S1074-7613(03)00175-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Peptide: MHC II complexes derived from a fluorescent antigen were detected in vivo to identify the cells that present subcutaneously injected antigen to CD4 T cells. Skin-derived dendritic cells (DCs) that acquired the antigen while in the draining lymph nodes were the first cells to display peptide:MHC II complexes. Presentation by these cells induced CD69, IL-2 production, and maximal proliferation by the T cells. Later, DCs displaying peptide:MHC II complexes migrated from the injection site via a G protein-dependent mechanism. Presentation by these migrants sustained expression of the IL-2 receptor and promoted delayed type hypersensitivity. Therefore, presentation of peptide:MHC II complexes derived from a subcutaneous antigen occurs in two temporally distinct waves with different functional consequences.
引用
收藏
页码:47 / 57
页数:11
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