与 TNFi 抗药抗体产生有关的因素及其对轴向脊柱关节炎的影响:两年随访研究

IF 1.3 Q4 RHEUMATOLOGY European journal of rheumatology Pub Date : 2024-10-14 DOI:10.5152/eurjrheum.2024.24013
Elif Durak Ediboğlu, Muhammed Çınar, Didem Kozacı, Dilek Solmaz, Gökhan Sargın, Ömer Karadağ, Gülay Kınıklı, Umut Kalyoncu, Sedat Yılmaz, Taşkın Şentürk, Gökhan Kabadayı, Gökhan Keser, Gülen Hatemi, Kübra Kaya, Mustafa Özmen, Figen Yargucu, Yeşim Özgüler, Ayşe Cefle, Önay Gerçik, Bünyamin Kısacık, Servet Akar
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引用次数: 0

摘要

目的评估肿瘤坏死因子抑制剂(TNFi)治疗的抗药性抗体(ADAb)在两年内的发展情况,并寻找与轴性脊柱关节炎(axSpA)患者相关的因素:这项观察性研究纳入了未接受生物治疗的 axSpA 患者。在治疗的第 12、24、52 和 104 周,通过酶联免疫吸附试验 (ELISA) 检测血清药物水平和 ADAb。采用广义估计方程(GEE)研究了随时间变化的 ADAb 发展情况以及与 ADAb 相关的因素:共纳入180例开始接受TNFi治疗的axSpA患者(男性116例,平均(±SD)45.6(±11.9)岁)(依那西普(32.2%)、阿达木单抗(27.2%)、戈利木单抗(20.6%)、英夫利昔单抗(20%))。在依那西普治疗组中,只有1名患者在12周和24周时出现了ADAb。阿达木单抗组32.7%的患者和英夫利昔单抗组21.2%的患者在12周时出现了针对TNFi药物的抗药物抗体,而且阿达木单抗和英夫利昔单抗治疗患者的ADAb阳性比例在整个随访期间保持稳定。在戈利木单抗组中,有一名患者在12周时出现了针对戈利木单抗的ADAb,在整个随访过程中,ADAb阳性患者的比例有所增加。在纵向分析中,基线年龄、TNFi类型、纵向巴斯强直性脊柱炎疾病活动指数(BASDAI)和ASDAS-CRP评分、血清C-eeactive蛋白(CRP)水平、不良事件的出现和治疗中断与ADAb的出现有关:结论:在为期两年的随访中,axSpA患者出现针对TNFi治疗的ADAb与年龄较小、疾病活动度较高、出现不良反应以及较常中断治疗有关。
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Factors Associated with the Development of Anti-drug Antibodies to TNFi and the Consequences for Axial Spondyloarthritis: A Two-year Follow-up Study.

Objective: To evaluate the development of anti-drug antibodies (ADAb) against tumor necrosis factor inhibitors (TNFi) therapy during a 2-year period and search the factors linked to patients with axial spondyloarthritis (axSpA).

Methods: Biologic-naive patients with axSpA were included in this observational study. Serum drug levels and ADAb were measured at weeks 12, 24, 52, and 104 of treatment by enzyme-linked immunosorbent assay (ELISA). The development of ADAb and factors related to ADAb over time were investigated using generalized estimating equations (GEE).

Results: A total of 180 patients with axSpA (116 male, mean (±SD) 45.6 (±11.9) years) who started TNFi treatment (etanercept (32.2%), adalimumab (27.2%), golimumab (20.6%), infliximab (20%)) were included. In the etanercept treatment group, only 1 patient had ADAb at 12 weeks and 24 weeks. Anti-drug antibodies against TNFi drugs were present in the adalimumab group in 32.7% of patients and in the infliximab group in 21.2% of patients at 12 weeks, and the proportion of ADAb-positive patients were found to be stable throughout the follow-up for adalimumab- and infliximab-treated patients. In the golimumab group, one patient had ADAb against golimumab at 12 weeks and the proportion of ADAb-positive patients increased throughout follow-up. In longitudinal analysis, baseline age, TNFi type, longitudinal Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) and ASDAS-CRP scores, serum C-eeactive protein (CRP) levels, presence of adverse events and treatment discontinuation were associated with the presence of ADAb.

Conclusion: The development of ADAb against TNFi therapy is associated with younger age, high disease activity, the development of adverse events and more common treatment discontinuation in patients with axSpA during 2-year follow-up.

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