Minghua Lyu , Pengtao Jiang , Bin Li , Zhifang Hu , Na Guo
{"title":"CD305 participates in abnormal activation of memory CD4+ T cells in patients with RA and attenuates collagen-induced arthritis","authors":"Minghua Lyu , Pengtao Jiang , Bin Li , Zhifang Hu , Na Guo","doi":"10.1016/j.molimm.2024.07.010","DOIUrl":null,"url":null,"abstract":"<div><p>Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease that mainly affects the joints. Studies have shown that memory CD4<sup>+</sup> T cells play an important role in the pathogenesis of RA. This study investigated the expression and function of CD305 on human memory CD4<sup>+</sup> T cells and the effects of CD305 activating antibody on collagen-induced arthritis. The results showed that CD305 expression was significantly decreased on circulating memory CD4<sup>+</sup> T cells from patients with RA and its mean fluorescence intensity (MFI) was negatively correlated with DAS28. Moreover, CD305 inhibited the activation of memory CD4<sup>+</sup> T cells by down-regulating CD69 and CD25 and the production of IFN-γ, IL-4, and IL-17A induced by anti-CD3/CD28 antibodies. In addition, activation of CD305 inhibited the severity of disease in collagen-induced arthritis. In summary, CD305 reduction may mediate the excessive activation of memory CD4<sup>+</sup> T cells and participate in the development of RA. It can be used as a predictive marker of disease activity and has potential medicinal value in the treatment of RA.</p></div>","PeriodicalId":3,"journal":{"name":"ACS Applied Electronic Materials","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Electronic Materials","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0161589024001378","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0
Abstract
Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease that mainly affects the joints. Studies have shown that memory CD4+ T cells play an important role in the pathogenesis of RA. This study investigated the expression and function of CD305 on human memory CD4+ T cells and the effects of CD305 activating antibody on collagen-induced arthritis. The results showed that CD305 expression was significantly decreased on circulating memory CD4+ T cells from patients with RA and its mean fluorescence intensity (MFI) was negatively correlated with DAS28. Moreover, CD305 inhibited the activation of memory CD4+ T cells by down-regulating CD69 and CD25 and the production of IFN-γ, IL-4, and IL-17A induced by anti-CD3/CD28 antibodies. In addition, activation of CD305 inhibited the severity of disease in collagen-induced arthritis. In summary, CD305 reduction may mediate the excessive activation of memory CD4+ T cells and participate in the development of RA. It can be used as a predictive marker of disease activity and has potential medicinal value in the treatment of RA.
类风湿性关节炎(RA)是一种主要影响关节的慢性全身性自身免疫性疾病。研究表明,记忆 CD4+ T 细胞在 RA 的发病机制中起着重要作用。本研究探讨了 CD305 在人类记忆 CD4+ T 细胞上的表达和功能,以及 CD305 激活抗体对胶原诱导的关节炎的影响。结果显示,CD305在RA患者循环记忆CD4+ T细胞上的表达明显下降,其平均荧光强度(MFI)与DAS28呈负相关。此外,CD305通过下调CD69和CD25以及抗CD3/CD28抗体诱导的IFN-γ、IL-4和IL-17A的产生,抑制了记忆CD4+ T细胞的活化。此外,激活 CD305 还能抑制胶原诱导的关节炎的病情严重程度。总之,CD305 的减少可能会介导记忆 CD4+ T 细胞的过度活化,并参与 RA 的发病。它可作为疾病活动性的预测标志物,在治疗 RA 方面具有潜在的药用价值。