Department of Immunology and Pathology, Central Clinical School, Monash University, Melbourne, VIC, Australia.
Department of Pharmacology and Therapeutics, Lung Health Research Centre, University of Melbourne, Melbourne, VIC, Australia.
Front Immunol. 2019 Jul 11;10:1597. doi: 10.3389/fimmu.2019.01597. eCollection 2019.
The lungs are continuously subjected to environmental insults making them susceptible to infection and injury. They are protected by the respiratory epithelium, which not only serves as a physical barrier but also a reactive one that can release cytokines, chemokines, and other defense proteins in response to danger signals, and can undergo conversion to protective mucus-producing goblet cells. The lungs are also guarded by a complex network of highly specialized immune cells and their mediators to support tissue homeostasis and resolve integrity deviation. This review focuses on specialized innate-like lymphocytes present in the lung that act as key sensors of lung insults and direct the pulmonary immune response. Included amongst these tissue-resident lymphocytes are innate lymphoid cells (ILCs), which are classified into five distinct subsets (natural killer, ILC1, ILC2, ILC3, lymphoid tissue-inducer cells), and unconventional T cells including natural killer T (NKT) cells, mucosal-associated invariant T (MAIT) cells, and γδ-T cells. While ILCs and unconventional T cells together comprise only a small proportion of the total immune cells in the lung, they have been found to promote lung homeostasis and are emerging as contributors to a variety of chronic lung diseases including pulmonary fibrosis, allergic airway inflammation, and chronic obstructive pulmonary disease (COPD). A particularly intriguing trait of ILCs that has recently emerged is their plasticity and ability to alter their gene expression profiles and adapt their function in response to environmental cues. The malleable nature of these cells may aid in rapid responses to pathogen but may also have downstream pathological consequences. The role of ILC2s in Th2 allergic airway responses is becoming apparent but the contribution of other ILCs and unconventional T cells during chronic lung inflammation is poorly described. This review presents an overview of our current understanding of the involvement of ILCs and unconventional T cells in chronic pulmonary diseases.
肺部不断受到环境侵袭,使其容易受到感染和损伤。肺部由呼吸上皮保护,呼吸上皮不仅起到物理屏障的作用,还能作为反应性屏障,在受到危险信号时释放细胞因子、趋化因子和其他防御蛋白,并能转化为保护性分泌黏液的杯状细胞。肺部还受到高度特化的免疫细胞及其介质的复杂网络的保护,以支持组织内稳态并解决完整性偏差。本综述重点介绍了存在于肺部的特化先天样淋巴细胞,它们作为肺部损伤的关键传感器,并指导肺部免疫反应。这些组织驻留淋巴细胞包括先天淋巴细胞(ILC),其分为五个不同亚群(自然杀伤细胞、ILC1、ILC2、ILC3、淋巴组织诱导细胞)和非常规 T 细胞,包括自然杀伤 T(NKT)细胞、黏膜相关不变 T(MAIT)细胞和γδ-T 细胞。虽然 ILC 和非常规 T 细胞一起仅占肺部总免疫细胞的一小部分,但它们被发现促进肺内稳态,并成为多种慢性肺部疾病(包括肺纤维化、过敏性气道炎症和慢性阻塞性肺疾病(COPD))的贡献者。最近出现的 ILC 的一个特别有趣的特征是它们的可塑性和改变其基因表达谱并根据环境线索改变其功能的能力。这些细胞的可塑性质可能有助于对病原体的快速反应,但也可能产生下游病理后果。ILC2 在 Th2 过敏气道反应中的作用正在变得明显,但其他 ILC 和非常规 T 细胞在慢性肺部炎症中的贡献描述得很少。本综述介绍了我们对 ILC 和非常规 T 细胞在慢性肺部疾病中的参与的现有理解。