Mohammed M. Kamil, M. Jabarah, Nizar A.l. Jasim
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引用次数: 0

摘要

背景:强直性脊柱炎是一种罕见的遗传性疾病。其治疗包括改变生活方式和使用药物,如生物制剂英夫利昔单抗或其生物类似物CT-P13英夫利单抗。尽管这些药物具有治疗作用,但仍会产生许多严重的不良反应,如免疫原性。目的:本研究的目的是调查生物类似物CT-P13英夫利昔单抗或原始英夫利单抗在伊拉克强直性脊柱炎患者中的免疫原性是否受到任何患者人口统计学特征的影响。方法:2021年12月至2022年3月,在巴格达教学医院/医疗城风湿病科进行了一项回顾性开放标签研究。在本研究中,44名患者正在服用英夫利昔单抗,另有50名患者在招募前服用CT-P13,剂量均为5mg/kg,持续3个月。疾病活性通过ASDAS-CRP评分进行评估,抗体和C反应蛋白通过酶联免疫吸附测定技术进行检测。使用社会科学20.0版的SPSS统计软件包进行统计分析。显著性水平为P0.05)。除了吸烟和疾病活性与抗CT-P13抗体的产生显著相关外,生物仿制药CT-P13英夫利昔单抗的数据相似(P<0.05),可能受到强直性脊柱炎患者的人口统计学特征或疾病活动的影响。
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Immunogenicity of the biosimilar CT-P13 infliximab or the original infliximab in Iraqi patients with Ankylosing spondylitis does not correlate with their demographic characteristics
Background: Ankylosing spondylitis is a rare disease affecting people with hereditary factors. Its treatment includes life style modification and use of drugs such as the biologic agent infliximab or its biosimilar, CT-P13 infliximab. Despite their therapeutic usefulness, these agents are associated with a number of serious adverse effects such as immunogenicity. Objectives: The aim of current study was to investigate if immunogenicity of the biosimilar CT-P13 infliximab or the original infliximab, in Iraqi patients with Ankylosing spondylitis, is affected by any of the patients’ demographic characteristics. Methods: A retrospective open-label study was conducted from December 2021 to March 2022 at the Rheumatology Unit, Baghdad Teaching Hospital/Medical City, Baghdad. Forty-four patients were taking Infliximab, and another 50 patients were taking CT-P13, both at a dose of 5mg/kg for 3 months prior to recruitment in current study. Disease activity was assessed by ASDAS-CRP score while antibodies and C-reactive protein were tested by Enzyme-Linked Immunosorbent Assay technique. Statistical analyses were performed using SPSS statistical package for Social Sciences version 20.0. The level of significance was considered at P<0.05. Results: There was non-significant correlation between anti-infliximab antibodies and demographic data of patients (P>0.05). Similar data were reported regarding the biosimilar CT-P13 infliximab except for smoking and disease activity which exhibited significant correlation with development of anti-CT-P13 antibodies (P<0.05). Conclusion: Immunogenicity of the biosimilar CT-P13 infliximab, but not that of the original Infliximab, may be influenced by demographic characteristics or disease activity in patients with ankylosing spondylitis.
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