Department of Immunology, University of Washington, Seattle, Wash.
Department of Immunology, University of Washington, Seattle, Wash; Benaroya Research Institute, Seattle, Wash.
J Allergy Clin Immunol. 2022 Dec;150(6):1302-1313. doi: 10.1016/j.jaci.2022.07.003. Epub 2022 Jul 19.
The release of cytokines from epithelial and stromal cells is critical for the initiation and maintenance of tissue immunity. Three such cytokines, thymic stromal lymphopoietin, IL-33, and IL-25, are important regulators of type 2 immune responses triggered by parasitic worms and allergens. In particular, these cytokines activate group 2 innate lymphoid cells, T2 cells, and myeloid cells, which drive hallmarks of type 2 immunity. However, emerging data indicate that these tissue-associated cytokines are not only involved in canonical type 2 responses but are also important in the context of viral infections, cancer, and even homeostasis. Here, we provide a brief review of the roles of thymic stromal lymphopoietin, IL-33, and IL-25 in diverse immune contexts, while highlighting their relative contributions in tissue-specific responses. We also emphasize a biologically motivated framework for thinking about the integration of multiple immune signals, including the 3 featured in this review.
细胞因子从上皮细胞和基质细胞中的释放对于组织免疫的启动和维持至关重要。三种这样的细胞因子,胸腺基质淋巴细胞生成素、IL-33 和 IL-25,是寄生虫和过敏原触发的 2 型免疫反应的重要调节剂。特别是,这些细胞因子激活了 2 型先天淋巴细胞、T2 细胞和髓样细胞,从而驱动 2 型免疫的特征。然而,新出现的数据表明,这些组织相关的细胞因子不仅参与了经典的 2 型反应,而且在病毒感染、癌症甚至体内平衡的情况下也很重要。在这里,我们简要回顾了胸腺基质淋巴细胞生成素、IL-33 和 IL-25 在不同免疫环境中的作用,同时强调了它们在组织特异性反应中的相对贡献。我们还强调了一个基于生物学的框架来思考包括本综述中介绍的三种细胞因子在内的多种免疫信号的整合。