Laboratoire d'Immunité Intestinale, Institut Imagine, INSERM U1163, Université Sorbonne Paris Cité, Paris, France.
Host-Microbiota Interaction, Institut Necker Enfants Malades, INSERM U1151, Université Sorbonne Paris Cité, Paris, France.
Mucosal Immunol. 2020 Sep;13(5):732-742. doi: 10.1038/s41385-020-0320-8. Epub 2020 Jul 10.
ILCs and T cells are closely related functionally but they significantly differ in their ability to circulate, expand, and renew. Cooperation and reciprocal functional regulation suggest that these cell types are more complementary than simply redundant during immune responses. How ILCs shape T-cell responses is strongly dependent on the tissue and inflammatory context. Likewise, indirect regulation of ILCs by adaptive immunity is induced by environmental cues such as the gut microbiota. Here, we review shared requirements for the development and function of both cell types and divergences in the orchestration of prototypic immune functions. We discuss the diversity of functional interactions between T cells and ILCs during homeostasis and immune responses. Identifying the location and the nature of the tissue microenvironment in which these interactions are taking place may uncover the remaining mysteries of their close encounters.
ILCs 和 T 细胞在功能上密切相关,但它们在循环、扩增和更新的能力上有显著差异。合作和相互的功能调节表明,在免疫反应中,这些细胞类型比简单的冗余更为互补。ILC 如何塑造 T 细胞反应强烈依赖于组织和炎症环境。同样,适应性免疫对 ILC 的间接调节是由环境线索诱导的,如肠道微生物群。在这里,我们回顾了这两种细胞类型的发育和功能的共同要求,以及在典型免疫功能的协调中的差异。我们讨论了 T 细胞和 ILC 之间在稳态和免疫反应中的功能相互作用的多样性。确定这些相互作用发生的位置和组织微环境的性质可能揭示它们密切接触的剩余谜团。