Department of Allergy and Clinical Immunology, National Research Institute for Child Health and Development, Tokyo, Japan.
Graduate School of Integrated Sciences for Life, Hiroshima University, Hiroshima, Japan.
Allergy. 2021 Nov;76(11):3332-3348. doi: 10.1111/all.14863. Epub 2021 May 5.
Discovery of innate lymphoid cells (ILCs), which are non-T and non-B lymphocytes that have no antigen-specific receptors, changed the classical concept of the mechanism of allergy, which had been explained mainly as antigen-specific acquired immunity based on IgE and Th2 cells. The discovery led to dramatic improvement in our understanding of the mechanism of non-IgE-mediated allergic inflammation. Numerous studies conducted in the past decade have elucidated the characteristics of each ILC subset in various organs and tissues and their ontogeny. We now know that each ILC subset exhibits heterogeneity. Moreover, the functions and activating/suppressing factors of each ILC subset were found to differ among both organs and types of tissue. Therefore, in this review, we summarize our current knowledge of ILCs by focusing on the organ/tissue-specific features of each subset to understand their roles in various organs. We also discuss ILCs' involvement in human inflammatory diseases in various organs and potential therapeutic/preventive strategies that target ILCs.
先天淋巴细胞 (ILC) 的发现改变了过敏机制的经典概念,这些先天淋巴细胞是无抗原特异性受体的非 T 细胞和非 B 细胞,过敏机制此前主要被解释为基于 IgE 和 Th2 细胞的抗原特异性获得性免疫。这一发现极大地提高了我们对非 IgE 介导的过敏炎症机制的理解。在过去的十年中,进行了许多研究,阐明了各个 ILC 亚群在各种器官和组织中的特征及其发生。我们现在知道每个 ILC 亚群都表现出异质性。此外,还发现每个 ILC 亚群的功能和激活/抑制因子在器官和组织类型之间存在差异。因此,在这篇综述中,我们通过关注每个亚群的器官/组织特异性特征来总结我们目前对 ILC 的认识,以了解它们在各种器官中的作用。我们还讨论了 ILC 在各种器官的人类炎症性疾病中的作用以及针对 ILC 的潜在治疗/预防策略。