Biomedical Sciences Graduate Program, College of Medicine, The Ohio State University, Columbus, OH.
Department of Microbial Infection and Immunity, College of Medicine, The Ohio State University, Columbus, OH.
J Immunol. 2022 Sep 1;209(5):845-854. doi: 10.4049/jimmunol.2200395.
Retinoic acid-inducible gene I-like receptors (RLRs) are cytosolic RNA sensors critical for initiation of antiviral immunity. Activation of RLRs following RNA recognition leads to production of antiviral genes and IFNs for induction of broad antiviral immunity. Although the RLRs are ubiquitously expressed, much of our understanding of these molecules comes from their study in epithelial cells and fibroblasts. However, RLR activation is critical for induction of immune function and long-term protective immunity. Recent work has focused on the roles of RLRs in immune cells and their contribution to programming of effective immune responses. This new understanding of RLR function in immune cells and immune programming has led to the development of vaccines and therapeutics targeting the RLRs. This review covers recent advances in our understanding of the contribution of RLRs to immune cell function during infection and the emerging RLR-targeting strategies for induction of immunity against cancer and viral infection.
视黄酸诱导基因 I 样受体 (RLRs) 是细胞溶质 RNA 传感器,对起始抗病毒免疫至关重要。RLRs 在 RNA 识别后被激活,导致抗病毒基因和 IFNs 的产生,从而诱导广泛的抗病毒免疫。尽管 RLRs 广泛表达,但我们对这些分子的大部分了解来自于它们在上皮细胞和成纤维细胞中的研究。然而,RLR 的激活对于诱导免疫功能和长期保护性免疫至关重要。最近的工作集中在 RLR 在免疫细胞中的作用及其对有效免疫反应的编程的贡献。对免疫细胞中 RLR 功能的这一新理解,导致了针对 RLR 的疫苗和治疗方法的发展。这篇综述涵盖了我们对 RLR 在感染过程中对免疫细胞功能的贡献的最新认识,以及新兴的 RLR 靶向策略,用于诱导对癌症和病毒感染的免疫。