Department of Immunology, Genetics and Pathology, The Rudbeck Laboratory, Uppsala University, Uppsala, Sweden.
Ups J Med Sci. 2024 Apr 12;129. doi: 10.48101/ujms.v129.10627. eCollection 2024.
Dendritic cells (DCs) possess a specialized function in presenting antigens and play pivotal roles in both innate and adaptive immune responses. Their ability to cross-present antigens from tumor cells to naïve T cells is instrumental in generating specific T-cell-mediated antitumor responses, crucial for controlling tumor growth and preventing tumor cell dissemination. However, within a tumor immune microenvironment (TIME), the functions of DCs can be significantly compromised. This review focuses on the profile, function, and activation of DCs, leveraging recent studies that reveal insights into their phenotype acquisition, transcriptional state, and functional programs through single-cell RNA sequence (scRNA-seq) analysis. Additionally, the therapeutic potential of DC-mediated tumor antigen sensing in priming antitumor immunity is discussed.
树突状细胞(DCs)在呈递抗原方面具有专门的功能,在先天和适应性免疫反应中发挥关键作用。它们将肿瘤细胞中的抗原交叉呈递给初始 T 细胞的能力对于产生特异性的 T 细胞介导的抗肿瘤反应至关重要,这对于控制肿瘤生长和防止肿瘤细胞扩散至关重要。然而,在肿瘤免疫微环境(TIME)中,DCs 的功能可能会受到严重影响。本综述重点介绍了 DCs 的特征、功能和激活,利用最近的研究揭示了通过单细胞 RNA 序列(scRNA-seq)分析获得的其表型获得、转录状态和功能程序的见解。此外,还讨论了 DC 介导的肿瘤抗原感应在启动抗肿瘤免疫中的治疗潜力。