Heat shock proteins and scavenger receptors: Role in adaptive immune responses

被引:24
作者
Facciponte, JG
MacDonald, IJ
Wang, XY
Kim, H
Manjili, MH
Subjeck, JR [1 ]
机构
[1] Roswell Pk Canc Inst, Dept Cellular Stress Biol, Buffalo, NY 14263 USA
[2] Roswell Pk Canc Inst, Dept Immunol, Buffalo, NY 14263 USA
[3] Roswell Pk Canc Inst, Dept Surg, Buffalo, NY 14263 USA
[4] Virginia Commonwealth Univ, Massey Canc Ctr, Dept Microbiol & Immunol, Richmond, VA 23284 USA
关键词
heat shock proteins; receptors; macrophages; dendritic cells; scavenger receptors; antigen presentation; cross-presentation; anti-tumor immunity;
D O I
10.1081/IMM-200064505
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumor-derived heat shock proteins have shown promise as anti-cancer vaccines in clinical trials. Heat shock proteins (HSPs) can generate potent anti-tumor immunity and elicit antigen-specific CD8(+) T cell responses in murine studies. Antigen presenting cells (APC), such as macrophages and dendritic cells (DCs), can elicit antigen-specific CD8(+) T cell responses mediated by HSPs. CD91 was the first identified endocytic scavenger receptor for HSPs on APC that can facilitate the process of cross-presentation. Other scavenger receptors may also play a similar role in this process. The present review critically evaluates the identified HSP endocytic receptors on APCs that may generate adaptive immune responses. A better understanding of this interaction between HSPs and APCs may further unravel mechanisms of immunoadjuvant function of HSPs.
引用
收藏
页码:325 / 342
页数:18
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