Involvement of LOX-1 in dendritic cell-mediated antigen cross-presentation

被引:404
作者
Delneste, Y
Magistrelli, G
Gauchat, JF
Haeuw, JF
Aubry, JP
Nakamura, K
Kawakami-Honda, N
Goetsch, L
Sawamura, T
Bonnefoy, JY
Jeannin, P
机构
[1] Ctr Immunol Pierre Fabre, F-74160 St Julien en Genevois, France
[2] Osaka Univ, Grad Sch Pharmaceut Sci, Dept Mol Pathophysiol, Suita, Osaka 5650871, Japan
[3] Natl Cardiovasc Ctr, Res Inst, Suita, Osaka 5658565, Japan
关键词
D O I
10.1016/S1074-7613(02)00388-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Some exogenous antigens, such as heat shock proteins or apoptotic bodies, gain access to the MHO class I processing pathway and initiate CTL responses, a process called cross-priming. To be efficient in vivo, this process requires endocytosis of the antigen by dendritic cells via receptors which remain unidentified. Here, we report that scavenger receptors are the main HSP binding structures on human dendritic cells and identify LOX-1 as one of these molecules. A neutralizing anti-LOX-1 mAb inhibits Hsp70 binding to dendritic cells and Hsp70-induced antigen cross-presentation. In vivo, to target LOX-1 with a tumor antigen using an anti-LOX-1 mAb induces antitumor immunity. Thus, the scavenger receptor LOX-1 is certainly a promising target for cancer immunotherapy.
引用
收藏
页码:353 / 362
页数:10
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