DEC-205 mediates antigen uptake and presentation by both resting and activated human plasmacytoid dendritic cells

被引:61
|
作者
Tel, Jurjen [1 ,2 ]
Benitez-Ribas, Daniel [1 ,2 ]
Hoosemans, Sander [1 ,2 ]
Cambi, Alessandra [1 ,2 ]
Adema, Gosse J. [1 ,2 ]
Figdor, Carl G. [1 ,2 ]
Tacken, Paul J. [1 ,2 ]
de Vries, I. Jolanda M. [1 ,2 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Tumor Immunol, NL-6500 HB Nijmegen, Netherlands
[2] Nijmegen Ctr Mol Life Sci, Nijmegen, Netherlands
关键词
Antigen presentation; DEC-205; Human pDCs; Targeting; TLR modulation; REGULATORY T-CELLS; COMPLEX CLASS-I; MHC CLASS-II; RECEPTOR DEC-205; MONOCLONAL-ANTIBODY; MELANOMA PATIENTS; LECTIN RECEPTORS; IMMUNE-RESPONSES; EXPRESSION; VIVO;
D O I
10.1002/eji.201040790
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
DEC-205 is a type I C-type lectin receptor (CLR) that is expressed on various APC subsets and has been suggested to bind necrotic and apoptotic cells. Here we study DEC-205 characteristics in plasmacytoid DCs (pDCs) obtained from healthy individuals and assess its ability to mediate antigen presentation by isolating sufficient numbers of pDCs from apheresis material obtained from stage III/IV melanoma patients. The results demonstrate that DEC-205 is expressed on human pDCs. Internalization of DEC-205 after antibody ligation is clathrin-and dynamin-dependent as it is blocked by hypertonic shock or by inhibition of dynamin activity. Antibody targeting to DEC-205 does not affect TLR-induced expression levels of co-stimulatory and MHC molecules, but clearly impairs TLR-induced IFN-alpha secretion by 40%. We observed that TLR-mediated signaling increases DEC-205 expression levels without affecting receptor internalization. Moreover, human pDCs retained the capacity to present antigens via DEC-205 following TLR activation.
引用
收藏
页码:1014 / 1023
页数:10
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