{"title":"Adipose tissue lymphocytes and obesity.","authors":"Feng Gao, Benjamin Litchfield, Huaizhu Wu","doi":"10.20517/jca.2023.38","DOIUrl":null,"url":null,"abstract":"<p><p>Obesity is associated with chronic inflammation in adipose tissue (AT), mainly evidenced by infiltration and phenotypic changes of various types of immune cells. Macrophages are the major innate immune cells and represent the predominant immune cell population within AT. Lymphocytes, including T cells and B cells, are adaptive immune cells and constitute another important immune cell population in AT. In obesity, CD8+ effector memory T cells, CD4+ Th1 cells, and B2 cells are increased in AT and promote AT inflammation, while regulatory T cells and Th2 cells, which usually function as immune regulatory or type 2 inflammatory cells, are reduced in AT. Immune cells may regulate the metabolism of adipocytes and other cells through various mechanisms, contributing to the development of metabolic diseases, including insulin resistance and type 2 diabetes. Efforts targeting immune cells and inflammation to prevent and treat obesity-linked metabolic disease have been explored, but have not yielded significant success in clinical studies. This review provides a concise overview of the changes in lymphocyte populations within AT and their potential role in AT inflammation and the regulation of metabolic functions in the context of obesity.</p>","PeriodicalId":75051,"journal":{"name":"The journal of cardiovascular aging","volume":"4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10919906/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The journal of cardiovascular aging","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20517/jca.2023.38","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/12/31 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Obesity is associated with chronic inflammation in adipose tissue (AT), mainly evidenced by infiltration and phenotypic changes of various types of immune cells. Macrophages are the major innate immune cells and represent the predominant immune cell population within AT. Lymphocytes, including T cells and B cells, are adaptive immune cells and constitute another important immune cell population in AT. In obesity, CD8+ effector memory T cells, CD4+ Th1 cells, and B2 cells are increased in AT and promote AT inflammation, while regulatory T cells and Th2 cells, which usually function as immune regulatory or type 2 inflammatory cells, are reduced in AT. Immune cells may regulate the metabolism of adipocytes and other cells through various mechanisms, contributing to the development of metabolic diseases, including insulin resistance and type 2 diabetes. Efforts targeting immune cells and inflammation to prevent and treat obesity-linked metabolic disease have been explored, but have not yielded significant success in clinical studies. This review provides a concise overview of the changes in lymphocyte populations within AT and their potential role in AT inflammation and the regulation of metabolic functions in the context of obesity.
肥胖与脂肪组织(AT)的慢性炎症有关,主要表现为各类免疫细胞的浸润和表型变化。巨噬细胞是主要的先天性免疫细胞,也是脂肪组织中最主要的免疫细胞群。淋巴细胞(包括 T 细胞和 B 细胞)是适应性免疫细胞,是 AT 中另一个重要的免疫细胞群。在肥胖症患者中,CD8+效应记忆T细胞、CD4+Th1细胞和B2细胞在AT中增多,并促进AT炎症,而通常作为免疫调节细胞或2型炎症细胞的调节性T细胞和Th2细胞在AT中减少。免疫细胞可通过各种机制调节脂肪细胞和其他细胞的新陈代谢,导致代谢性疾病的发生,包括胰岛素抵抗和 2 型糖尿病。针对免疫细胞和炎症来预防和治疗与肥胖有关的代谢性疾病的研究一直在进行,但在临床研究中并未取得显著的成功。本综述简明扼要地概述了肥胖引起的血管内淋巴细胞群的变化及其在血管内炎症和代谢功能调节中的潜在作用。