Immunology of Infectious Diseases Research Center, Research Institute of Basic Medical Sciences, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Department of Clinical Biochemistry, School of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.
Inflammopharmacology. 2023 Dec;31(6):3021-3028. doi: 10.1007/s10787-023-01289-8. Epub 2023 Jul 15.
The therapeutic profile of the patients with rheumatoid arthritis (RA) commonly consists of immunosuppressive and anti-inflammatory compounds. Here in this research, we assessed the potential effect of drug treatment in the RA patients in increasing the risk of coronavirus disease 2019 (COVID-19) infection.
In this retrospective cross-sectional study, 200 subjects with RA were recruited. The treatment profile of the subjects for the past 6 months was collected. The COVID-19 diagnosis was implemented based on the standard molecular tests and clinical examinations. Serum concentration of cytokines was measured using enzyme-linked immunosorbent assay (ELISA).
It was detected that there was an increased risk of COVID-19 in RA subjects receiving Etanercept (OR = 3.51, 95% CI 1.19-10.30, P = 0.022). Concentrations of Interleukin (IL)-1β, Interferon (IFN)-γ, Tumor necrosis factor (TNF)-α, IL-6, IL-17A, and IL-23 were significantly higher in the RA patients with COVID-19 relative to RA cases without COVID-19. In RA/COVID-19 cases receiving Etanercept, serum levels of TNF-α, IL-1β, and IL-6 were significantly lower than RA/COVID-19 subjects without Etanercept therapy.
It seems that Etanercept therapy in RA cases might increase proneness of the COVID-19 risk in these cases. The mechanism of this increased risk may stem from suppressing a protective immunity state in the RA cases.
类风湿关节炎(RA)患者的治疗方案通常包括免疫抑制剂和抗炎化合物。在这项研究中,我们评估了药物治疗对 RA 患者感染 2019 冠状病毒病(COVID-19)风险的潜在影响。
在这项回顾性横断面研究中,招募了 200 名 RA 患者。收集了患者过去 6 个月的治疗方案。COVID-19 的诊断是基于标准的分子测试和临床检查。使用酶联免疫吸附试验(ELISA)测量细胞因子的血清浓度。
发现接受依那西普(Etanercept)治疗的 RA 患者 COVID-19 感染风险增加(OR=3.51,95%CI 1.19-10.30,P=0.022)。与未感染 COVID-19 的 RA 患者相比,感染 COVID-19 的 RA 患者的白细胞介素(IL)-1β、干扰素(IFN)-γ、肿瘤坏死因子(TNF)-α、IL-6、IL-17A 和 IL-23 浓度明显升高。在接受依那西普治疗的 RA/COVID-19 患者中,TNF-α、IL-1β 和 IL-6 的血清水平明显低于未接受依那西普治疗的 RA/COVID-19 患者。
依那西普治疗似乎会增加 RA 患者感染 COVID-19 的风险。这种风险增加的机制可能源于抑制 RA 患者的保护性免疫状态。