启动(农业)
蛋白酶体
交叉展示
抗原
细胞毒性T细胞
T细胞
CD8型
细胞生物学
肽
细胞
化学
生物
免疫系统
生物化学
免疫学
体外
MHC I级
发芽
植物
作者
Christopher C. Norbury,Sameh Basta,Keri B. Donohue,David C. Tscharke,Michael F. Princiotta,Peter Berglund,James S. Gibbs,Jack R. Bennink,Jonathan W. Yewdell
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2004-05-27
卷期号:304 (5675): 1318-1321
被引量:287
标识
DOI:10.1126/science.1096378
摘要
“Cross-priming” describes the activation of naïve CD8 + T cells by professional antigen-presenting cells that have acquired viral or tumor antigens from “donor” cells. Antigen transfer is believed to be mediated by donor cell–derived molecular chaperones bearing short peptide ligands generated by proteasome degradation of protein antigens. We show here that cross-priming is based on the transfer of proteasome substrates rather than peptides. These findings are potentially important for the rational design of vaccines that elicit CD8 + T cell responses.
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