Lin Sen, Gao Wei, Sun Jiachen, Gao Kai, Li Dan, Mei Xifan
Department of Orthopedics, Third Affiliated Hospital of Jinzhou Medical University, Jinzhou, PR China.
Key Laboratory of Medical Tissue Engineering, Jinzhou Medical University, Jinzhou, PR China.
Mater Today Bio. 2022 Jun 23;15:100331. doi: 10.1016/j.mtbio.2022.100331. eCollection 2022 Jun.
Rheumatoid arthritis (RA) is an autoimmune-mediated inflammatory disease that seriously threatens patients' life. Different stages of RA require different treatments, but the accurate classification of the RA remains challenging. Herein, we conducted an in-depth study of 73 RA patients to investigate RA development. CD 19, a biomarker of B cell dysfunction, was found to be strongly associated with the development of severe symptoms. On the other hand, CD19 was significantly reduced, when effective clinical treatment relieved the symptoms. Therefore, it is proposed that B cell-inducing factors are important for the development of RA to the advanced stage and can be used to assist in the accurate classification of RA development. Furthermore, we speculated that drugs that could properly modulate B cells might have efficacy in advanced-stage RA. From this perspective, R-dihydrolipoic acid (R-DHLA)-stabilized cerium-modified gold nanoclusters (AuNCs) (R-DHLA-AuNCs-Ce) (∼3.4 nm) were developed for comprehensive treatment of advanced-stage RA. According to our established rat models of collagen-induced arthritis (CIA), R-DHLA-AuNCs-Ce restored the comprehensive changes of cytokines to a normal state by regulating B cell activity within 24 h. Furthermore, the immune responses elicited by B cells were memory-suppressed after detachment from R-DHLA-AuNCs-Ce and the advanced symptoms of RA in CIA rats were successfully reversed to a healthy state. Compared to clinical drugs such as methotrexate (MTX) and etanercept, R-DHLA-AuNCs-Ce were found to more efficiently suppress B cell immunity mitigating advanced-stage RA.
类风湿性关节炎(RA)是一种由自身免疫介导的炎症性疾病,严重威胁患者生命。RA的不同阶段需要不同的治疗方法,但RA的准确分类仍然具有挑战性。在此,我们对73例RA患者进行了深入研究以调查RA的发展情况。发现B细胞功能障碍的生物标志物CD 19与严重症状的发展密切相关。另一方面,当有效的临床治疗缓解症状时,CD19显著降低。因此,有人提出B细胞诱导因子对RA发展到晚期很重要,可用于辅助RA发展的准确分类。此外,我们推测能够适当调节B细胞的药物可能对晚期RA有效。从这个角度出发,开发了R-二氢硫辛酸(R-DHLA)稳定的铈修饰金纳米团簇(AuNCs)(R-DHLA-AuNCs-Ce)(约3.4纳米)用于晚期RA的综合治疗。根据我们建立的胶原诱导性关节炎(CIA)大鼠模型,R-DHLA-AuNCs-Ce在24小时内通过调节B细胞活性将细胞因子的综合变化恢复到正常状态。此外,B细胞引发的免疫反应在与R-DHLA-AuNCs-Ce分离后被记忆抑制,CIA大鼠的RA晚期症状成功逆转至健康状态。与甲氨蝶呤(MTX)和依那西普等临床药物相比,发现R-DHLA-AuNCs-Ce能更有效地抑制B细胞免疫以减轻晚期RA。