Joan and Sanford I. Weill Department of Medicine, Division of Gastroenterology, Weill Cornell Medicine, New York, New York.
Department of Microbiology and Immunology, Weill Cornell Medicine, New York, New York.
Immunol Rev. 2018 Nov;286(1):137-147. doi: 10.1111/imr.12703.
Innate and adaptive lymphocytes employ diverse effector programs that provide optimal immunity to pathogens and orchestrate tissue homeostasis, or conversely can become dysregulated to drive progression of chronic inflammatory diseases. Emerging evidence suggests that CD4 T helper cell subsets and their innate counterparts, the innate lymphoid cell family, accomplish these complex biological roles by selectively programming their cellular metabolism in order to instruct distinct modules of lymphocyte differentiation, proliferation, and cytokine production. Further, these metabolic pathways are significantly influenced by tissue microenvironments and disease states. Here, we summarize our current knowledge on how cell-intrinsic metabolic factors modulate the context-dependent bioenergetic pathways that govern innate and adaptive lymphocytes. Further, we propose that a greater understanding of these pathways may lead to the identification of unique features in each population and provoke the development of novel therapeutic strategies to modulate lymphocytes in health and disease.
先天和适应性淋巴细胞采用多种效应程序,为病原体提供最佳免疫,并协调组织动态平衡,或者相反,它们可能失调,导致慢性炎症性疾病的进展。新出现的证据表明,CD4 T 辅助细胞亚群及其先天对应物,即先天淋巴细胞家族,通过选择性地对其细胞代谢进行编程来完成这些复杂的生物学作用,以便指导淋巴细胞分化、增殖和细胞因子产生的不同模块。此外,这些代谢途径受组织微环境和疾病状态的显著影响。在这里,我们总结了我们目前对细胞内在代谢因素如何调节控制先天和适应性淋巴细胞的与上下文相关的生物能量途径的了解。此外,我们提出,对这些途径的更好理解可能会导致在每个群体中识别出独特的特征,并引发开发新的治疗策略来调节健康和疾病中的淋巴细胞。