甲氨蝶呤类风湿性关节炎患者BNT162b2 mRNA COVID-19疫苗接种后抗刺突抗体滴度的时间过程

Satoshi Shinohara, Yasuhiro Hirose
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引用次数: 0

摘要

甲氨蝶呤是类风湿性关节炎的锚定药物,它会阻碍mRNA COVID-19疫苗的免疫原性。因此,类风湿关节炎患者接受甲氨蝶呤的最佳疫苗策略是至关重要的。我们监测了7名医护人员和1名接受甲氨蝶呤治疗的类风湿性关节炎患者接种BNT162b2 mRNA COVID-19疫苗后的抗刺突抗体滴度。医护人员抗刺突抗体滴度在初次接种后立即显著升高后继续降低,而类风湿关节炎患者抗刺突抗体滴度在初次接种后立即显著降低后升高。所有参与者的滴度在加强后1个月显著增加。随着时间的推移,这些变化可能表明,在甲氨蝶呤治疗的类风湿性关节炎患者中,短寿命浆细胞的产生被强烈抑制;相比之下,长寿命浆细胞和记忆B细胞的产生是完整的。对于甲氨蝶呤治疗的类风湿性关节炎患者,重要的是要完成初级和加强系列疫苗接种,以确保对COVID-19有足够的免疫力。
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Time Course of Antispike Antibody Titer after Administration of BNT162b2 mRNA COVID-19 Vaccine in a Patient with Rheumatoid Arthritis on Methotrexate.

Methotrexate, an anchor drug for rheumatoid arthritis, hinders the immunogenicity of mRNA COVID-19 vaccines. Therefore, an optimal vaccine strategy for patients with rheumatoid arthritis receiving methotrexate is vital. We monitored antispike antibody titers after BNT162b2 mRNA COVID-19 vaccination in seven healthcare workers and one methotrexate-treated rheumatoid arthritis patient. The antispike antibody titers of healthcare workers significantly increased immediately after primary vaccination and then continued to decrease, whereas those of the rheumatoid arthritis patient were significantly lower immediately after primary vaccination and then increased. The titers in all participants dramatically increased 1-month postbooster. These changes over time may suggest that in the methotrexate-treated rheumatoid arthritis patient, the generation of short-lived plasma cells was strongly suppressed; in contrast, the generation of long-lived plasma cells and memory B cells was intact. For methotrexate-treated rheumatoid arthritis patients, it is important to complete the primary and booster vaccination series to ensure sufficient immunity against COVID-19.

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审稿时长
12 weeks
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