Yasuda Shinsuke
Department of Rheumatology, Endocrinology and Nephrology Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Japan.
Clin Calcium. 2018;28(5):668-676.
CTLA4 abolishes interaction between CD28 on T cells and B7 molecules on antigen presenting cells. CTLA4-Ig, abatacept(ABT)was developed as a drug with multipotent inhibitor against activated T/B cells, monocytes, dendritic cells, macrophages and osteoclast progenitors expressing B7 molecules. In phase Ⅲ RCTs, clinical effects of ABT have been established in MTX-naive, MTX-IR and TNF inhibitor-IR patients with RA. Moreover, in head-to head comparison with representative TNF inhibitors, ABT exerted compatible clinical effect. In clinical practice, ABT is recognized as a biological DMARD with good safety profile. Reduction or withdrawal of ABT is also proposed in patients who achieved remission under treatment with ABT+MTX. In conclusion, ABT can be included in the treatment strategy of RA with wide clinical variance.
CTLA4可消除T细胞上的CD28与抗原呈递细胞上的B7分子之间的相互作用。CTLA4-Ig阿巴西普(ABT)被开发为一种对表达B7分子的活化T/B细胞、单核细胞、树突状细胞、巨噬细胞和破骨细胞祖细胞具有多效抑制作用的药物。在Ⅲ期随机对照试验中,ABT在未使用甲氨蝶呤(MTX)、MTX反应不佳和肿瘤坏死因子(TNF)抑制剂反应不佳的类风湿关节炎(RA)患者中已确立了临床疗效。此外,在与代表性TNF抑制剂的头对头比较中,ABT发挥了相当的临床效果。在临床实践中,ABT被认为是一种安全性良好的生物性改善病情抗风湿药(DMARD)。对于在ABT+MTX治疗下实现缓解的患者,也建议减少或停用ABT。总之,ABT可纳入具有广泛临床差异的RA治疗策略中。