Princess Margaret Cancer Centre, University Health Network, University of Toronto, 610 University Ave., Toronto, Ontario, M5G 2M9, Canada; Campbell Family Institute for Breast Cancer Research, Canada.
Princess Margaret Cancer Centre, University Health Network, University of Toronto, 610 University Ave., Toronto, Ontario, M5G 2M9, Canada; Campbell Family Institute for Breast Cancer Research, Canada; Department of Immunology, University of Toronto, Canada.
Semin Immunol. 2019 Feb;41:101284. doi: 10.1016/j.smim.2019.101284. Epub 2019 Aug 2.
The tumor microenvironment is shaped by interactions between tumor cells, stroma, and immune cells. T cells are a critical component of the immunological anti-tumor response and most immunotherapeutic approaches in cancer aim to augment T cell responses. Recently, innate lymphoid cells (ILCs) have been added to the list of cell populations that influence T cell responses within the tumor microenvironment. ILCs were shown to modulate T cell functions through a variety of mechanisms. However, the impact of ILC and T cell interactions on disease outcome appears to be contextual as their phenotype and function is strongly influenced by the local tissue microenvironment. Here we focus on recent advances in understanding the mechanisms of ILCs in regulating T cell responses in inflammatory diseases and cancer.
肿瘤微环境由肿瘤细胞、基质和免疫细胞之间的相互作用塑造。T 细胞是免疫抗肿瘤反应的关键组成部分,癌症中的大多数免疫治疗方法旨在增强 T 细胞反应。最近,先天淋巴细胞 (ILC) 已被添加到影响肿瘤微环境中 T 细胞反应的细胞群体列表中。已经表明 ILC 通过多种机制调节 T 细胞功能。然而,ILC 和 T 细胞相互作用对疾病结果的影响似乎是上下文相关的,因为它们的表型和功能受到局部组织微环境的强烈影响。在这里,我们专注于理解 ILC 调节炎症性疾病和癌症中 T 细胞反应的机制的最新进展。