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老年类风湿关节炎患者同时接受甲氨蝶呤治疗会降低对 SARS-CoV-2 mRNA 疫苗的第三剂(加强针)体液免疫反应。

Reduced humoral response to a third dose (booster) of SARS-CoV-2 mRNA vaccines by concomitant methotrexate therapy in elderly patients with rheumatoid arthritis.

机构信息

Department I of Internal Medicine, University of Cologne, Koln, Germany.

Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf, Cologne, Germany.

出版信息

RMD Open. 2022 Oct;8(2). doi: 10.1136/rmdopen-2022-002632.

Abstract

BACKGROUND

Several health authorities recommend a third (booster) vaccination to protect patients with rheumatic and musculoskeletal diseases from severe COVID-19. Methotrexate has been shown to reduce the efficacy of the first and second dose of SARS-CoV-2 mRNA vaccines. So far, it remains unknown how concomitant methotrexate affects the efficacy of a COVID-19 booster vaccination.

METHODS

We compared the humoral immune response to SARS-CoV-2 vaccination in 136 patients with rheumatoid arthritis (RA) treated with methotrexate and/or biological or targeted synthetic (b/tsDMARDs). IgG targeting the receptor binding domain (RBD) of SARS-CoV-2 spike protein was measured at a median of 52.5 (range 2-147) days after a third dose of the SARS-CoV-2 mRNA vaccines BNT162b2 or mRNA-1273.

RESULTS

Anti-RBD IgG was significantly reduced in elderly patients receiving concomitant treatment with methotrexate as compared with elderly patients receiving monotherapy with b/tsDMARDs or methotrexate (64.8 (20.8, 600.3) binding antibody units per mL (BAU/mL) vs 1106.0 (526.3, 4965.2) BAU/mL vs 1743.8 (734.5, 6779.6) BAU/mL, median (IQR), p<0.001, Kruskal-Wallis test). In younger patients (< 64.5 years), concomitant methotrexate had no significant impact on the humoral immune response.

CONCLUSIONS

Concomitant methotrexate increases the risk of an insufficient humoral immune response to SARS-CoV-2 vaccination in elderly patients with RA. Pausing methotrexate during the third vaccination period may be considered for this group of patients.

摘要

背景

一些卫生机构建议对风湿和肌肉骨骼疾病患者进行第三次(加强)疫苗接种,以预防严重的 COVID-19。甲氨蝶呤已被证明会降低 SARS-CoV-2 mRNA 疫苗第一和第二剂的效力。迄今为止,尚不清楚同时使用甲氨蝶呤如何影响 COVID-19 加强疫苗接种的效果。

方法

我们比较了 136 例接受甲氨蝶呤和/或生物或靶向合成(b/tsDMARDs)治疗的类风湿关节炎(RA)患者接种 SARS-CoV-2 疫苗后的体液免疫反应。在第三次接种 SARS-CoV-2 mRNA 疫苗 BNT162b2 或 mRNA-1273 后中位数为 52.5(范围 2-147)天,测量针对 SARS-CoV-2 刺突蛋白受体结合域(RBD)的 IgG。

结果

与接受 b/tsDMARDs 或甲氨蝶呤单药治疗的老年患者相比,同时接受甲氨蝶呤治疗的老年患者的抗-RBD IgG 显著降低(64.8(20.8,600.3)结合抗体单位/毫升(BAU/mL)比 1106.0(526.3,4965.2)BAU/mL 比 1743.8(734.5,6779.6)BAU/mL,中位数(IQR),p<0.001,Kruskal-Wallis 检验)。在较年轻的患者(<64.5 岁)中,同时使用甲氨蝶呤对体液免疫反应没有显著影响。

结论

同时使用甲氨蝶呤会增加老年 RA 患者对 SARS-CoV-2 疫苗接种产生低体液免疫反应的风险。对于这组患者,可能需要在第三剂疫苗接种期间暂停甲氨蝶呤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/495b/9556739/6caa1ccd4a9f/rmdopen-2022-002632f01.jpg

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