David Reyes-Leiva, Joaquín López-Contreras, Esther Moga, Francesc Pla-Juncà, Elionor Lynton-Pons, Ricardo Rojas-Garcia, Janina Turon-Sans, Luis Querol, Montse Olive, Rodrigo Álvarez-Velasco, Marta Caballero-Ávila, Álvaro Carbayo, Ana Vesperinas-Castro, Pere Domingo, Isabel Illa, Eduard Gallardo, Elena Cortés-Vicente
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引用次数: 12
Abstract
Background and objectives: Evidence regarding the safety and efficacy of messenger RNA (mRNA) vaccines in patients with myasthenia gravis (MG) after immunosuppressive therapies is scarce. Our aim is to determine whether the mRNA-1273 vaccine is safe and able to induce humoral and cellular responses in patients with MG.
Methods: We performed an observational, longitudinal, prospective study including 100 patients with MG of a referral center for MG in our country, conducted from April 2021 to November 2021 during the vaccination campaign. The mRNA-1273 vaccine was scheduled for all participants. Blood samples were collected before vaccination and 3 months after a second dose. Clinical changes in MG were measured using the MG activities of daily life score at baseline and 1 week after the first and second doses. A surveillance of all symptoms of coronavirus disease 2019 (COVID-19) was conducted throughout the study. Humoral and cellular immune responses after vaccination were assessed using a spike-antibody ELISA and interferon gamma release assay in plasma. The primary outcomes were clinically significant changes in MG symptoms after vaccination, adverse events (AEs), and seroconversion and T-cell immune response rates.
Results: Ninety-nine patients completed the full vaccination schedule, and 98 had 2 blood samples taken. A statistically significant worsening of symptoms was identified after the first and second doses of the mRNA-1273 vaccine, but this was not clinically relevant. Mild AEs occurred in 14 patients after the first dose and in 21 patients after the second dose. Eighty-seven patients developed a humoral response and 72 patients showed a T-cell response after vaccination. A combined therapy with prednisone and other immunosuppressive drugs correlated with a lower seroconversion ratio (OR = 5.97, 95% CI 1.46-24.09, p = 0.015) and a lower T-cell response ratio (OR = 2.83, 95% CI 1.13-7.13, p = 0.024).
Discussion: Our findings indicate that the mRNA vaccination against COVID-19 is safe in patients with MG and show no negative impact on the disease course. Patients achieved high humoral and cellular immune response levels.
Classification of evidence: This study provides Class IV evidence that patients with MG receiving the mRNA-1273 vaccine did not show clinical worsening after vaccination and that most of the patients achieved high cellular or immune response levels.
背景和目的:关于信使RNA (mRNA)疫苗在免疫抑制治疗后重症肌无力(MG)患者中的安全性和有效性的证据很少。我们的目的是确定mRNA-1273疫苗是否安全,是否能够在MG患者中诱导体液和细胞反应。方法:我们进行了一项观察性、纵向、前瞻性研究,包括2021年4月至2021年11月期间在我国一家MG转诊中心进行的100例MG患者。mRNA-1273疫苗计划为所有参与者接种。在接种疫苗前和第二次接种后3个月采集血样。在基线和第一次和第二次给药后1周,使用MG日常生活活动评分来测量MG的临床变化。在整个研究过程中对2019冠状病毒病(COVID-19)的所有症状进行了监测。接种疫苗后的体液和细胞免疫反应采用尖峰抗体ELISA和血浆干扰素γ释放试验进行评估。主要结局是疫苗接种后MG症状、不良事件(ae)、血清转化和t细胞免疫应答率的临床显著变化。结果:99例患者完成了完整的疫苗接种计划,98例患者采集了2份血液样本。在第一次和第二次接种mRNA-1273疫苗后,发现了统计学上显著的症状恶化,但这与临床无关。14例患者在第一次给药后发生轻度不良反应,21例患者在第二次给药后发生轻度不良反应。接种疫苗后,87名患者出现体液应答,72名患者出现t细胞应答。强尼松联合其他免疫抑制药物治疗与较低的血清转换率(OR = 5.97, 95% CI 1.46-24.09, p = 0.015)和较低的t细胞应答率(OR = 2.83, 95% CI 1.13-7.13, p = 0.024)相关。讨论:我们的研究结果表明,针对COVID-19的mRNA疫苗接种在MG患者中是安全的,并且对病程没有负面影响。患者达到了较高的体液和细胞免疫应答水平。证据分类:本研究提供IV类证据,表明接受mRNA-1273疫苗的MG患者在接种后没有出现临床恶化,并且大多数患者达到了较高的细胞或免疫应答水平。