抗原
主要组织相容性复合体
骨髓
免疫学
抗原呈递
MHC I级
CD8型
生物
启动(农业)
细胞毒性T细胞
人类白细胞抗原
Pan-T抗原
免疫系统
癌症研究
T细胞
抗体
单克隆抗体
体外
遗传学
发芽
植物
作者
Alex Y. Huang,Paul T. Golumbek,Mojgan Ahmadzadeh,Elizabeth M. Jaffee,Drew M. Pardoll,Hyam I. Levitsky
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1994-05-13
卷期号:264 (5161): 961-965
被引量:1189
标识
DOI:10.1126/science.7513904
摘要
Many tumors express tumor-specific antigens capable of being presented to CD8+ T cells by major histocompatibility complex (MHC) class I molecules. Antigen presentation models predict that the tumor cell itself should present these antigens to T cells. However, when conditions for the priming of tumor-specific responses were examined in mice, no detectable presentation of MHC class I-restricted tumor antigens by the tumor itself was found. Rather, tumor antigens were exclusively presented by host bone marrow-derived cells. Thus, MHC class I-restricted antigens are efficiently transferred in vivo to bone marrow-derived antigen-presenting cells, which suggests that human leukocyte antigen matching may be less critical in the application of tumor vaccines than previously thought.
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