Rodriguez Pedro C, Torres-Moya Roberto, Reyes Gil, Molinero Claudino, Prada Dinorah, Lopez Ana M, Hernandez Isabel M, Hernandez Maria V, Martinez Jose P, Hernandez Xochel, Casaco Angel, Ramos Mayra, Avila Yisel, Barrese Yinet, Montero Enrique, Hernandez Patricia
Clinical Research Division, Center of Molecular Immunology, Havana, Cuba.
National Service for Rheumatology, Havana, Cuba.
Results Immunol. 2012 Nov 21;2:204-11. doi: 10.1016/j.rinim.2012.11.001. eCollection 2012.
T cells are involved in the pathogenesis of rheumatoid arthritis (RA). CD6 is a co-stimulatory molecule, predominantly expressed on lymphocytes, that has been linked to autoreactive responses. The purpose of this study was to evaluate the safety, immunogenicity and preliminary efficacy of itolizumab, a humanized anti-CD6 monoclonal antibody, in patients with active rheumatoid arthritis. Fifteen patients were enrolled in a phase I, open-label, dose-finding study. Five cohorts of patients received a weekly antibody monotherapy with a dose-range from 0.1 to 0.8 mg/kg. Itolizumab showed a good safety profile, with no severe or serious adverse events reported so far. No signs or symptoms associated with immunosuppression were observed in the study. Objective clinical responses were achieved in more than 80% of patients after treatment completion, and these responses tend to be sustained afterwards. This clinical study constitutes the first evidence of the safety and positive clinical effect of a monotherapy using an anti-CD6 antibody in patients with rheumatoid arthritis.
T细胞参与类风湿关节炎(RA)的发病机制。CD6是一种共刺激分子,主要表达于淋巴细胞,与自身反应性应答有关。本研究的目的是评估人源化抗CD6单克隆抗体艾托珠单抗在活动性类风湿关节炎患者中的安全性、免疫原性和初步疗效。15名患者参加了一项I期开放标签剂量探索研究。五组患者接受每周一次的抗体单药治疗,剂量范围为0.1至0.8mg/kg。艾托珠单抗显示出良好的安全性,迄今为止未报告严重或重大不良事件。研究中未观察到与免疫抑制相关的体征或症状。超过80%的患者在治疗完成后实现了客观临床反应,且这些反应在之后往往得以持续。这项临床研究构成了使用抗CD6抗体单药治疗类风湿关节炎患者安全性和积极临床效果的首个证据。