Anno Shohei, Inui Kentaro, Tada Masahiro, Sugioka Yuko, Okano Tadashi, Mamoto Kenji, Koike Tatsuya
Departments of Orthopaedic Surgery, Yodogawa Christian Hospital, Osaka, Japan.
Departments of Orthopaedic Surgery, Osaka Metropolitan University Medical School, Osaka, Japan.
J Rheum Dis. 2025 Jul 1;32(3):182-189. doi: 10.4078/jrd.2024.0130. Epub 2025 Feb 3.
Previous studies reported that abatacept (ABT) decreased autoantibodies in early rheumatoid arthritis (RA) patients. We investigated the impact of ABT, and other biological disease-modifying anti-rheumatic drugs (bDMARDs) on autoantibody levels in established RA patients.
This prospective observational study included 50 RA patients treated with ABT and 115 RA patients treated with non-ABT bDMARDs. Serum levels of anticitrullinated peptide antibodies (ACPA), immunoglobulin (Ig) M-rheumatoid factor (IgM-RF), IgG-RF, and anti-agalactosyl IgG antibody (anti-Gal (0) IgG) were measured at baseline and after 48 weeks of treatment.
After propensity score matching, 25 patients with ABT and 25 patients with non-ABT were finally analyzed. Disease activity score in 28 joints using C-reactive protein significantly decreased in both ABT group (4.5 to 3.3, p<0.01) and non-ABT group (4.4 to 2.5, p<0.01) after 48 weeks treatment. In ABT group, median titers at baseline and 48 weeks were 62.7 and 57.8 U/mL for ACPA (p=0.22), 35.0 and 39.0 IU/mL for IgM-RF (p=0.21), 0.5 and 0.5 IU/mL for IgG-RF (p=0.19), and 50.4 and 53.5 AU/mL for anti-Gal (0) IgG (p=0.22), respectively. Changes of all autoantibody titer were not significant in ABT group. Non-ABT group showed significant decreases in ACPA (baseline 143.0 to 57.8 U/mL at week 48, p=0.03), IgM-RF (50.0 to 37.0 IU/mL, p<0.01), and anti-Gal (0) IgG (93.2 to 61.8 AU/mL, p<0.01) except IgG-RF (0.6 to 0.5 IU/mL, p=0.22).
Autoantibody-lowering effect of ABT was not strong in established RA patients in our study.
既往研究报道阿巴西普(ABT)可降低早期类风湿关节炎(RA)患者的自身抗体水平。我们研究了ABT及其他生物性改善病情抗风湿药(bDMARDs)对确诊RA患者自身抗体水平的影响。
这项前瞻性观察性研究纳入了50例接受ABT治疗的RA患者和115例接受非ABT bDMARDs治疗的RA患者。在基线及治疗48周后检测血清抗瓜氨酸化肽抗体(ACPA)、免疫球蛋白(Ig)M类风湿因子(IgM-RF)、IgG类风湿因子(IgG-RF)及抗半乳糖基IgG抗体(抗-Gal(0)IgG)水平。
经过倾向评分匹配后,最终分析了25例接受ABT治疗的患者和25例接受非ABT治疗的患者。治疗48周后,ABT组(4.5至3.3,p<0.01)和非ABT组(4.4至2.5,p<0.01)使用C反应蛋白的28关节疾病活动评分均显著降低。在ABT组中,ACPA基线和48周时的中位滴度分别为62.7和57.8 U/mL(p=0.22),IgM-RF为35.0和(39.0)IU/mL(p=0.21),IgG-RF为0.5和0.5 IU/mL(p=0.19),抗-Gal(0)IgG为50.4和53.5 AU/mL(p=0.22)。ABT组所有自身抗体滴度变化均不显著。非ABT组ACPA(基线143.0至48周时的57.8 U/mL,p=0.03)、IgM-RF(50.0至37.0 IU/mL,p<0.01)及抗-Gal(0)IgG(93.2至61.8 AU/mL,p<0.01)显著降低,IgG-RF除外(0.6至0.5 IU/mL,p=0.22)。
在我们的研究中,ABT对确诊RA患者的自身抗体降低作用不强。