Medical Research Council, Laboratory of Molecular Biology, Cambridge, Cambridgeshire, CB2 0QH, United Kingdom; email:
Annu Rev Immunol. 2021 Apr 26;39:167-198. doi: 10.1146/annurev-immunol-110119-091711. Epub 2021 Feb 3.
Type 2 immunity helps protect the host from infection, but it also plays key roles in tissue homeostasis, metabolism, and repair. Unfortunately, inappropriate type 2 immune reactions may lead to allergy and asthma. Group 2 innate lymphoid cells (ILC2s) in the lungs respond rapidly to local environmental cues, such as the release of epithelium-derived type 2 initiator cytokines/alarmins, producing type 2 effector cytokines such as IL-4, IL-5, and IL-13 in response to tissue damage and infection. ILC2s are associated with the severity of allergic asthma, and experimental models of lung inflammation have shown how they act as playmakers, receiving signals variously from stromal and immune cells as well as the nervous system and then distributing cytokine cues to elicit type 2 immune effector functions and potentiate CD4 T helper cell activation, both of which characterize the pathology of allergic asthma. Recent breakthroughs identifying stromal- and neuronal-derived microenvironmental cues that regulate ILC2s, along with studies recognizing the potential plasticity of ILC2s, have improved our understanding of the immunoregulation of asthma and opened new avenues for drug discovery.
2 型免疫有助于宿主免受感染,但它也在组织稳态、代谢和修复中发挥关键作用。不幸的是,不适当的 2 型免疫反应可能导致过敏和哮喘。肺部的 2 型先天淋巴样细胞(ILC2)对局部环境线索(如上皮细胞衍生的 2 型起始细胞因子/警报素的释放)快速作出反应,在组织损伤和感染时产生 2 型效应细胞因子,如 IL-4、IL-5 和 IL-13。ILC2 与过敏性哮喘的严重程度有关,肺部炎症的实验模型表明它们如何作为推动者发挥作用,从基质和免疫细胞以及神经系统接收各种信号,然后分配细胞因子线索,引发 2 型免疫效应功能,并增强 CD4 T 辅助细胞的激活,这两者都是过敏性哮喘病理的特征。最近在确定调节 ILC2 的基质和神经元衍生的微环境线索方面取得的突破,以及认识到 ILC2 潜在可塑性的研究,提高了我们对哮喘免疫调节的理解,并为药物发现开辟了新途径。