医学
托珠单抗
CX3CL1型
类风湿性关节炎
阿达木单抗
内科学
去整合素
胃肠病学
痹症科
金属蛋白酶
免疫学
趋化因子
炎症
基质金属蛋白酶
趋化因子受体
作者
Takeo Isozaki,Shinichiro Nishimi,Airi Nishimi,Mayu Saito,Yusuke Miwa,Yoichi Toyoshima,Katsunori Inagaki,Tsuyoshi Kasama
标识
DOI:10.1080/14397595.2016.1256025
摘要
A disintegrin and metalloproteinase (ADAM)-10 is expressed in rheumatoid arthritis (RA). In this study, we focused on ADAM-10 as a predictive factor for the treatment with biologics in RA.The levels of ADAM-10 and fractalkine/CX3CL1 in RA and healthy controls serum were measured using enzyme-linked immunosorbent assays. Fifteen patients were treated with adalimumab (ADA), and 20 patients were treated with tocilizumab (TCZ).ADAM-10 positively correlated with fractalkine/CX3CL1 in the sera of RA patients and was presented at a significantly higher level compared to that in normal serum (487 ± 80 pg/ml and 85 ± 33 pg/ml, respectively, p < 0.05). ADAM-10 highly correlates with fractalkine/CX3CL1 in the sera of RA patients. The level of ADAM-10 decreased after the treatment with TCZ but not with ADA. In addition, we found that the level of ADAM-10 in TCZ responders was significantly higher than that of the TCZ nonresponders at 24 weeks (619 ± 134 pg/ml and 109 ± 25 pg/ml, respectively). Multiple regression analysis showed that ADAM-10 was only identified as independent predictive variable for the improvement of DAS28 (ESR) at 24 weeks.ADAM-10 may be a predictor of the effectiveness of TCZ in treating RA.
科研通智能强力驱动
Strongly Powered by AbleSci AI