Hitchon Carol A, Bowdish Dawn M E, Boire Gilles, Fortin Paul R, Flamand Louis, Chandran Vinod, Dayam Roya M, Gingras Anne-Claude, Card Catherine M, Colmegna Inés, Larché Maggie J, Kaplan Gilaad G, Lukusa Luck, Lee Jennifer L F, Bernatsky Sasha
Department of Internal Medicine, Max Rady College of Medicine, Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
McMaster Immunology Research Centre, McMaster University, Hamilton, ON L8S 4L8, Canada.
Vaccines (Basel). 2024 Sep 17;12(9):1061. doi: 10.3390/vaccines12091061.
SARS-CoV-2 remains the third most common cause of death in North America. We studied the effects of methotrexate and tumor necrosis factor inhibitor (TNFi) on neutralization responses after COVID-19 vaccination in immune-mediated inflammatory disease (IMID). Prospective data and sera of adults with inflammatory bowel disease (IBD), rheumatoid arthritis (RA), spondyloarthritis (SpA), psoriatic arthritis (PsA), and systemic lupus (SLE) were collected at six academic centers in Alberta, Manitoba, Ontario, and Quebec between 2022 and 2023. Sera from two time points were evaluated for each subject. Neutralization studies were divided between five laboratories, and each lab's results were analyzed separately using multivariate generalized logit models (ordinal outcomes: absent, low, medium, and high neutralization). Odds ratios (ORs) for the effects of methotrexate and TNFi were adjusted for demographics, IMID, other biologics and immunosuppressives, prednisone, COVID-19 vaccinations (number/type), and infections in the 6 months prior to sampling. The adjusted ORs for methotrexate and TNFi were then pooled in random-effects meta-analyses (separately for the ancestral strains and the Omicron BA1 and BA5 strains). Of 479 individuals (958 samples), 292 (61%) were IBD, 141 (29.4%) were RA, and the remainder were PsA, SpA, and SLE. The mean age was 57 (62.2% female). For both the individual labs and the meta-analyses, the adjusted ORs suggested independent negative effects of TNFi and methotrexate on neutralization. The meta-analysis adjusted ORs for TNFi were 0.56 (95% confidence interval (CI) 0.39, 0.81) for the ancestral strain and 0.56 (95% CI 0.39, 0.81) for BA5. The meta-analysis adjusted OR for methotrexate was 0.39 (95% CI 0.19, 0.76) for BA1. SARS-CoV-2 neutralization in vaccinated IMID was diminished independently by TNFi and methotrexate. As SARS-CoV-2 circulation continues, ongoing vigilance regarding optimized vaccination is required.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)仍是北美第三大常见死因。我们研究了甲氨蝶呤和肿瘤坏死因子抑制剂(TNFi)对免疫介导的炎症性疾病(IMID)患者接种新冠病毒疫苗后中和反应的影响。2022年至2023年期间,在艾伯塔省、曼尼托巴省、安大略省和魁北克省的六个学术中心收集了患有炎症性肠病(IBD)、类风湿性关节炎(RA)、脊柱关节炎(SpA)、银屑病关节炎(PsA)和系统性红斑狼疮(SLE)的成年人的前瞻性数据和血清。对每个受试者两个时间点的血清进行评估。中和研究在五个实验室之间进行,每个实验室的结果分别使用多变量广义logit模型进行分析(有序结果:无、低、中和高中和)。甲氨蝶呤和TNFi作用的比值比(OR)针对人口统计学、IMID、其他生物制剂和免疫抑制剂、泼尼松、新冠病毒疫苗接种(数量/类型)以及采样前6个月内的感染情况进行了调整。然后,将甲氨蝶呤和TNFi的调整后OR合并到随机效应荟萃分析中(分别针对原始毒株以及奥密克戎BA1和BA5毒株)。在479名个体(958份样本)中,292名(61%)患有IBD,141名(29.4%)患有RA,其余为PsA、SpA和SLE。平均年龄为57岁(女性占62.2%)。对于各个实验室以及荟萃分析,调整后的OR表明TNFi和甲氨蝶呤对中和有独立的负面影响。TNFi的荟萃分析调整后OR对于原始毒株为0.56(95%置信区间(CI)0.39,0.81),对于BA5为0.56(95%CI 0.39,0.81)。甲氨蝶呤的荟萃分析调整后OR对于BA1为0.39(95%CI 0.19,0.76)。在接种疫苗的IMID患者中,TNFi和甲氨蝶呤独立降低了SARS-CoV-2中和作用。随着SARS-CoV-2继续传播,需要持续警惕优化疫苗接种。