Godoy-Tena Gerard, Ballestar Esteban
Epigenetics and Immune Disease Group, Josep Carreras Research Institute (IJC), 08916 Barcelona, Spain.
Epigenetics in Inflammatory and Metabolic Diseases Laboratory, Health Science Center (HSC), East China Normal University (ECNU), Shanghai 200241, China.
Cancers (Basel). 2022 Feb 24;14(5):1179. doi: 10.3390/cancers14051179.
Dendritic cells (DCs) are professional antigen-presenting cells with the distinctive property of inducing the priming and differentiation of naïve CD4+ and CD8+ T cells into helper and cytotoxic effector T cells to develop efficient tumor-immune responses. DCs display pathogenic and tumorigenic antigens on their surface through major histocompatibility complexes to directly influence the differentiation of T cells. Cells in the tumor microenvironment (TME), including cancer cells and other immune-infiltrated cells, can lead DCs to acquire an immune-tolerogenic phenotype that facilitates tumor progression. Epigenetic alterations contribute to cancer development, not only by directly affecting cancer cells, but also by their fundamental role in the differentiation of DCs that acquire a tolerogenic phenotype that, in turn, suppresses T cell-mediated responses. In this review, we focus on the epigenetic regulation of DCs that have infiltrated the TME and discuss how knowledge of the epigenetic control of DCs can be used to improve DC-based vaccines for cancer immunotherapy.
树突状细胞(DCs)是专业的抗原呈递细胞,具有独特的特性,能够诱导初始CD4+和CD8+ T细胞启动并分化为辅助性和细胞毒性效应T细胞,从而产生有效的肿瘤免疫反应。DCs通过主要组织相容性复合体在其表面展示致病性和肿瘤igenic抗原,直接影响T细胞的分化。肿瘤微环境(TME)中的细胞,包括癌细胞和其他免疫浸润细胞,可导致DCs获得促进肿瘤进展的免疫耐受性表型。表观遗传改变不仅通过直接影响癌细胞,还通过其在DCs分化中的基本作用,促使DCs获得耐受性表型,进而抑制T细胞介导的反应,从而促进癌症发展。在本综述中,我们聚焦于浸润到TME中的DCs的表观遗传调控,并讨论如何利用对DCs表观遗传控制的了解来改进基于DCs的癌症免疫治疗疫苗。