Schäfer Arne, Kovacs Magdolna S, Eder Anna, Nigg Axel, Feuchtenberger Martin
Diabetes Zentrum Mergentheim, Bad Mergentheim, Germany.
Medizinische Klinik und Poliklinik II, University Hospital Würzburg, Würzburg, Germany.
Rheumatol Adv Pract. 2023 Jul 26;7(2):rkad065. doi: 10.1093/rap/rkad065. eCollection 2023.
Several studies on the immunogenicity of vaccination against coronavirus disease 2019 (COVID-19) in patients with immune-mediated inflammatory diseases have evaluated the influence of DMARDs. The aim of the work presented here was to compare the humoral vaccine response after two vaccinations between patients with RA undergoing TNF inhibitor therapy and healthy controls.
We assessed the humoral immune response, as measured by titres of neutralizing antibodies against the S1 antigen of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), in patients with RA and anti-TNF treatment . controls without immunomodulatory medication. One hundred and seven fully vaccinated individuals were included at 6 ± 1 weeks after the second vaccination [BioNTech/Pfizer (72.9%), AstraZeneca (17.8%) and Moderna (9.3%)]. Immune responses in terms of antibody titres were compared between both subgroups with ( = 45) and without ( = 62) exposure to anti-TNF medication. The comparison was performed as a cross-sectional, single-centre study approach using non-parametric tests for central tendency.
Anti-TNF medication produced a significantly impaired humoral immune response to vaccination against COVID-19. The maximum immune response was detected in 77.4% of control patients, whereas this decreased to 62.2% in participants treated with TNF inhibitors ( = 0.045; effect size, = 0.194). Patients on combination treatment (anti-TNF medication and MTX, 17 of 45 subjects in the treatment group) did not differ significantly regarding humoral immune response compared with patients on monotherapy with TNF inhibitors only ( = 0.214).
TNF inhibitors significantly reduce the humoral response following dual vaccination against COVID-19 in patients with RA.
多项关于2019冠状病毒病(COVID-19)疫苗接种在免疫介导的炎症性疾病患者中的免疫原性研究评估了改善病情抗风湿药(DMARDs)的影响。本文介绍的这项研究的目的是比较接受肿瘤坏死因子(TNF)抑制剂治疗的类风湿关节炎(RA)患者和健康对照者在两次接种疫苗后的体液免疫反应。
我们评估了RA患者和接受抗TNF治疗的对照者(未使用免疫调节药物)针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)S1抗原的中和抗体滴度所测得的体液免疫反应。在第二次接种疫苗后6±1周纳入了107名完全接种疫苗的个体[辉瑞/BioNTech(72.9%)、阿斯利康(17.8%)和莫德纳(9.3%)]。比较了暴露于抗TNF药物(n = 45)和未暴露于抗TNF药物(n = 62)的两个亚组之间的抗体滴度免疫反应。采用非参数检验集中趋势的横断面单中心研究方法进行比较。
抗TNF药物显著损害了针对COVID-19疫苗接种的体液免疫反应。77.4%的对照患者检测到最大免疫反应,而在接受TNF抑制剂治疗的参与者中这一比例降至62.2%(P = 0.045;效应量,r = 0.194)。联合治疗患者(抗TNF药物和甲氨蝶呤,治疗组45名受试者中的17名)与仅接受TNF抑制剂单药治疗的患者相比,体液免疫反应无显著差异(P = 0.214)。
TNF抑制剂显著降低了RA患者针对COVID-19的两次疫苗接种后的体液免疫反应。