{"title":"MAIT cells modulating the oral lichen planus immune microenvironment: a cellular crosstalk perspective.","authors":"Qian Mi, Xiaoli Wu, Yuhe Chen, Wenxia Meng","doi":"10.1007/s00011-024-01990-6","DOIUrl":null,"url":null,"abstract":"<p><p>Mucosal-associated invariant T (MAIT) cells, a type of T lymphocytes with innate-like characteristics, are crucial in bridging innate and adaptive immunity. When activated, MAIT cells release various inflammatory molecules and swiftly respond to antigens. Notably, numerous studies highlight the significant impact of MAIT cells on tumors and various immune disorders by influencing the immune microenvironment. Oral lichen planus (OLP) is an immune-mediated inflammatory condition mainly involving T lymphocytes. Previous research primarily focused on T cells alone, neglecting the broader immune environment. However, there is a current growing recognition of the complex interactions among multiple immune cells and inflammatory factors in patients with OLP. This immune microenvironment comprises T lymphocytes, fibroblasts, keratinocytes, dendritic cells, macrophages, inflammation-related cytokines, and chemokines, orchestrating intricate interactions that contribute to OLP initiation and persistence. Therefore, this review consolidates current research on the interplay between MAIT cells and other immune cells within the OLP microenvironment. We also delve into potential mechanisms through which MAIT cells regulate inflammation in patients with OLP, aiming to further explore the role of MAIT cells in these patients.</p>","PeriodicalId":13550,"journal":{"name":"Inflammation Research","volume":"74 1","pages":"10"},"PeriodicalIF":4.8000,"publicationDate":"2025-01-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inflammation Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00011-024-01990-6","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Mucosal-associated invariant T (MAIT) cells, a type of T lymphocytes with innate-like characteristics, are crucial in bridging innate and adaptive immunity. When activated, MAIT cells release various inflammatory molecules and swiftly respond to antigens. Notably, numerous studies highlight the significant impact of MAIT cells on tumors and various immune disorders by influencing the immune microenvironment. Oral lichen planus (OLP) is an immune-mediated inflammatory condition mainly involving T lymphocytes. Previous research primarily focused on T cells alone, neglecting the broader immune environment. However, there is a current growing recognition of the complex interactions among multiple immune cells and inflammatory factors in patients with OLP. This immune microenvironment comprises T lymphocytes, fibroblasts, keratinocytes, dendritic cells, macrophages, inflammation-related cytokines, and chemokines, orchestrating intricate interactions that contribute to OLP initiation and persistence. Therefore, this review consolidates current research on the interplay between MAIT cells and other immune cells within the OLP microenvironment. We also delve into potential mechanisms through which MAIT cells regulate inflammation in patients with OLP, aiming to further explore the role of MAIT cells in these patients.
mucal -associated invariant T (MAIT)细胞是一种具有先天样特征的T淋巴细胞,在桥接先天免疫和适应性免疫中起着至关重要的作用。当被激活时,MAIT细胞释放各种炎症分子并迅速对抗原作出反应。值得注意的是,许多研究强调了MAIT细胞通过影响免疫微环境对肿瘤和各种免疫疾病的重要影响。口腔扁平苔藓(OLP)是一种免疫介导的炎症,主要涉及T淋巴细胞。以前的研究主要集中在单独的T细胞上,而忽略了更广泛的免疫环境。然而,目前越来越多的人认识到OLP患者中多种免疫细胞和炎症因子之间的复杂相互作用。这种免疫微环境包括T淋巴细胞、成纤维细胞、角质形成细胞、树突状细胞、巨噬细胞、炎症相关细胞因子和趋化因子,它们协调复杂的相互作用,促进OLP的发生和持续。因此,本综述整合了目前关于MAIT细胞与OLP微环境中其他免疫细胞之间相互作用的研究。我们还深入研究了MAIT细胞在OLP患者中调节炎症的潜在机制,旨在进一步探讨MAIT细胞在这些患者中的作用。
期刊介绍:
Inflammation Research (IR) publishes peer-reviewed papers on all aspects of inflammation and related fields including histopathology, immunological mechanisms, gene expression, mediators, experimental models, clinical investigations and the effect of drugs. Related fields are broadly defined and include for instance, allergy and asthma, shock, pain, joint damage, skin disease as well as clinical trials of relevant drugs.