Immunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Immunobiology Laboratory, The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.
Semin Immunol. 2023 Mar;66:101726. doi: 10.1016/j.smim.2023.101726. Epub 2023 Feb 7.
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.
传统树突状细胞 1 型 (cDC1) 对于诱导针对肿瘤和病毒抗原的保护性 CD8 T 细胞反应至关重要。在许多情况下,cDC1 以从死亡的肿瘤或病毒感染的细胞内化的物质形式获取这些抗原。cDC1 如何提取与死亡细胞相关的抗原,并以与 MHC Ⅰ类分子结合的肽形式呈递这些抗原以激活 CD8 T 细胞仍不清楚。在这里,我们回顾树突状细胞自然杀伤组受体 1(DNGR-1;也称为 CLEC9A)的生物学特性,DNGR-1 是一种在 cDC1 上高度表达的 C 型凝集素受体,在这个过程中起着关键作用。我们强调了最近的进展,这些进展支持了 DNGR-1 信号在促进含有死亡细胞碎片的吞噬或内吞隔室的诱导性破裂中的作用,从而使与死亡细胞相关的抗原可被 cDC1 内源性 MHC Ⅰ类加工和呈递机制识别。我们进一步回顾了 DNGR-1 如何检测死亡细胞,以及该受体在抗病毒和抗肿瘤免疫中的功能。最后,我们强调了 DNGR-1 的研究如何为交叉呈递开辟了新的视角,其中一些可能在癌症的免疫治疗和抗病毒疫苗接种中有应用。