交叉展示
MHC I级
抗原呈递
生物
抗原
CD8型
抗原处理
细胞毒性T细胞
免疫学
抗原提呈细胞
CD1型
细胞生物学
树突状细胞
免疫疗法
主要组织相容性复合体
免疫系统
T细胞
自然杀伤性T细胞
生物化学
体外
作者
Conor M. Henry,Carlos A. Castellanos,Caetano Reis e Sousa
标识
DOI:10.1016/j.smim.2023.101726
摘要
Conventional dendritic cells type 1 (cDC1) are critical for inducing protective CD8+ T cell responses to tumour and viral antigens. In many instances, cDC1 access those antigens in the form of material internalised from dying tumour or virally-infected cells. How cDC1 extract dead cell-associated antigens and cross-present them in the form of peptides bound to MHC class I molecules to CD8+ T cells remains unclear. Here we review the biology of dendritic cell natural killer group receptor-1 (DNGR-1; also known as CLEC9A), a C-type lectin receptor highly expressed on cDC1 that plays a key role in this process. We highlight recent advances that support a function for DNGR-1 signalling in promoting inducible rupture of phagocytic or endocytic compartments containing dead cell debris, thereby making dead cell-associated antigens accessible to the endogenous MHC class I processing and presentation machinery of cDC1. We further review how DNGR-1 detects dead cells, as well as the functions of the receptor in anti-viral and anti-tumour immunity. Finally, we highlight how the study of DNGR-1 has opened new perspectives into cross-presentation, some of which may have applications in immunotherapy of cancer and vaccination against viral diseases.
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