Boosting antibody responses by targeting antigens to dendritic cells

被引:76
作者
Caminschi, Irina [1 ,2 ]
Shortman, Ken [1 ,3 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Melbourne, Vic 3052, Australia
[2] Univ Melbourne, Dept Microbiol & Immunol, Melbourne, Vic, Australia
[3] Univ Melbourne, Dept Med Biol, Melbourne, Vic, Australia
关键词
C-TYPE LECTIN; CD8(+) T-CELLS; SUBSETS IN-VIVO; CROSS-PRESENTATION; DC-SIGN; ANTITUMOR IMMUNITY; B-LYMPHOCYTES; RECEPTOR; INDUCTION; ACTIVATION;
D O I
10.1016/j.it.2011.10.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Delivering antigens directly to dendritic cells (DCs) in situ, by injecting antigens coupled to antibodies specific for DC surface molecules, is a promising strategy for enhancing vaccine efficacy. Enhanced cytotoxic T cell responses are obtained if an adjuvant is co-administered to activate the DC. Such DC targeting is also effective at enhancing humoral immunity, via the generation of T follicular helper cells. Depending on the DC surface molecule targeted, antibody production can be enhanced even in the absence of adjuvants. In the case of Clec9A as the DC surface target, enhanced antibody production is a consequence of the DC-restricted expression of the target molecule. Few other cells absorb the antigen antibody construct, therefore, it persists in the bloodstream, allowing sustained antigen presentation, even by non-activated DCs.
引用
收藏
页码:71 / 77
页数:7
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