微泡
抗原
外体
淋巴结
树突状细胞
细胞生物学
小泡
滤泡树突状细胞
肿瘤细胞
抗原提呈细胞
生物
肿瘤抗原
癌症研究
化学
免疫学
T细胞
免疫疗法
免疫系统
小RNA
基因
遗传学
膜
作者
Megan K. Ruhland,Edward W. Roberts,En Cai,Adriana M. Mujal,Kyle Marchuk,Casey Beppler,David Nam,Nina K. Serwas,Mikhail Binnewies,Matthew F. Krummel
出处
期刊:Cancer Cell
[Elsevier]
日期:2020-06-01
卷期号:37 (6): 786-799.e5
被引量:165
标识
DOI:10.1016/j.ccell.2020.05.002
摘要
Generation of tumor-infiltrating lymphocytes begins when tumor antigens reach the lymph node (LN) to stimulate T cells, yet we know little of how tumor material is disseminated among the large variety of antigen-presenting dendritic cell (DC) subsets in the LN. Here, we demonstrate that tumor proteins are carried to the LN within discrete vesicles inside DCs and are then transferred among DC subsets. A synapse is formed between interacting DCs and vesicle transfer takes place in the absence of free exosomes. DCs -containing vesicles can uniquely activate T cells, whereas DCs lacking them do not. Understanding this restricted sharing of tumor identity provides substantial room for engineering better anti-tumor immunity.
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