Immunopathogenesis Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland 20852, USA.
Immunology Discovery, Genentech, Inc., 1 DNA Way, South San Francisco, California 94080, USA.
Nat Rev Immunol. 2018 Jan;18(1):62-76. doi: 10.1038/nri.2017.90. Epub 2017 Aug 30.
Type 2 immunity is characterized by the production of IL-4, IL-5, IL-9 and IL-13, and this immune response is commonly observed in tissues during allergic inflammation or infection with helminth parasites. However, many of the key cell types associated with type 2 immune responses - including T helper 2 cells, eosinophils, mast cells, basophils, type 2 innate lymphoid cells and IL-4- and IL-13-activated macrophages - also regulate tissue repair following injury. Indeed, these cell populations engage in crucial protective activity by reducing tissue inflammation and activating important tissue-regenerative mechanisms. Nevertheless, when type 2 cytokine-mediated repair processes become chronic, over-exuberant or dysregulated, they can also contribute to the development of pathological fibrosis in many different organ systems. In this Review, we discuss the mechanisms by which type 2 immunity contributes to tissue regeneration and fibrosis following injury.
2 型免疫的特征是产生白细胞介素 4(IL-4)、白细胞介素 5(IL-5)、白细胞介素 9(IL-9)和白细胞介素 13(IL-13),这种免疫反应通常在过敏炎症或寄生虫感染时在组织中观察到。然而,许多与 2 型免疫反应相关的关键细胞类型——包括辅助性 T 细胞 2(Th2)细胞、嗜酸性粒细胞、肥大细胞、嗜碱性粒细胞、2 型先天淋巴细胞和 IL-4 和 IL-13 激活的巨噬细胞——也调节损伤后的组织修复。事实上,这些细胞群体通过减少组织炎症和激活重要的组织再生机制,参与了至关重要的保护活动。然而,当 2 型细胞因子介导的修复过程变得慢性、过度活跃或失调时,它们也可能导致许多不同器官系统中病理性纤维化的发展。在这篇综述中,我们讨论了 2 型免疫如何促进损伤后的组织再生和纤维化。