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针对多发性硬化症患者的 SARS-CoV-2 灭活疫苗和 mRNA 疫苗的安全性和体液免疫应答率。

Safety and humoral response rate of inactivated and mRNA vaccines against SARS-CoV-2 in patients with Multiple Sclerosis.

机构信息

Neurology, Pontificia Universidad Católica de Chile, Santiago, Chile; Neurology, Hospital Sótero del Río, Santiago, Chile.

Neurology, Pontificia Universidad Católica de Chile, Santiago, Chile; Neurology, Hospital Sótero del Río, Santiago, Chile.

出版信息

Mult Scler Relat Disord. 2022 Mar;59:103690. doi: 10.1016/j.msard.2022.103690. Epub 2022 Feb 13.

Abstract

BACKGROUND

Safety and effectiveness outcomes in Multiple Sclerosis (MS) patients receiving different disease-modifying therapies (DMT) and different types of vaccines against SARS-CoV-2 are limited. Growing evidence coming mainly from Israel, Europe and North America using mRNA and adenoviral vector vaccines has been published.

OBJECTIVES

To assess the safety and humoral response of inactivated virus and mRNA vaccines against SARS-CoV-2 in patients with MS.

METHODS

Ongoing, multicentric, prospective, observational study performed between February and September 2021. Humoral response (antibodies against spike-1 protein) was determined at least 4 weeks after the complete schedule of anti-SARS-CoV-2 vaccines. Categorical outcome (positive/negative) and total antibody titres were recorded. Adverse events supposedly attributable to vaccination (AESAV) were collected.

RESULTS

178 patients, 68% women, mean age 39.7 ± 11.2 years, 123 received inactivated (Coronavac-Sinovac), 51 mRNA (Pfizer-BioNtech), and 4 adenoviral vector vaccines (CanSino n = 2, Jonhson&Johnson-Jannsen n = 1, Oxford-AstraZeneca n = 1). Six patients had a history of COVID-19 before vaccination. Overall humoral response was observed in 66.9% (62.6% inactivated vs. 78.4% mRNA, p = 0.04). Positive anti-S1-antibodies were observed in 100% of patients with no DMT (n = 3), 100% with interferon/glatiramer-acetate (n = 11), 100% with teriflunomide/dimethyl-fumarate (n = 16), 100% with natalizumab (n = 10), 100% with alemtuzumab (n = 8), 90% with cladribine (n = 10), and 88% with fingolimod (n = 17), while 43% of patients receiving antiCD20 (n = 99) were positive (38% inactivated vaccine vs. 59% mRNA vaccine, p = 0.05). In the multivariate analysis including antiCD20 patients, the predictors for a positive humoral response were receiving the mRNA vaccine (OR 8.11 (1.79-36.8), p = 0.007) and a lower number of total infusions (OR 0.44 (0.27-0.74) p = 0.002. The most frequent AESAV was local pain (14%), with 4 (2.2%) patients experiencing mild-moderate relapses within 8 weeks of first vaccination compared to 11 relapses (6.2%) within the 8 weeks before vaccination (Chi-squared 3.41, p = 0.06).

DISCUSSION

A higher humoral response rate was observed using the mRNA compared to the inactivated vaccine, while patients using antiCD20 had a significantly lower response rate, and patients using antiCD20 and fingolimod had lower antibody titres. In this MS patient cohort, inactivated and mRNA vaccines against SARS-CoV-2 appear to be safe, with no increase in relapse rate. This information may help guidelines including booster shots and types of vaccines in selected populations.

摘要

背景

接受不同疾病修正疗法 (DMT) 和针对 SARS-CoV-2 的不同类型疫苗的多发性硬化症 (MS) 患者的安全性和有效性结果有限。主要来自以色列、欧洲和北美的越来越多的证据使用 mRNA 和腺病毒载体疫苗已经发表。

目的

评估接受 MS 患者的灭活病毒和 mRNA 疫苗对 SARS-CoV-2 的安全性和体液反应。

方法

正在进行的、多中心、前瞻性、观察性研究于 2021 年 2 月至 9 月进行。在完成针对 SARS-CoV-2 疫苗的完整计划后至少 4 周确定体液反应(针对刺突蛋白-1 的抗体)。记录分类结局(阳性/阴性)和总抗体滴度。收集推测与疫苗接种相关的不良事件 (AESAV)。

结果

178 名患者,68%为女性,平均年龄 39.7±11.2 岁,123 名患者接受了灭活(科兴)疫苗,51 名患者接受了 mRNA(辉瑞-生物科技)疫苗,4 名患者接受了腺病毒载体疫苗(康希诺 n=2,强生&约翰逊-Jannsen n=1,牛津-阿斯利康 n=1)。6 名患者在接种疫苗前有 COVID-19 病史。总体体液反应率为 66.9%(灭活疫苗为 62.6%,mRNA 疫苗为 78.4%,p=0.04)。无 DMT(n=3)、干扰素/格拉替雷-乙酸酯(n=11)、特立氟胺/二甲基富马酸盐(n=16)、那他珠单抗(n=10)、阿仑单抗(n=8)、氯苯丁酸(n=10)的患者中均观察到 100%的患者存在抗 S1 抗体),而接受抗 CD20 治疗的患者(n=99)中 43%为阳性(抗 CD20 治疗患者中灭活疫苗为 38%,mRNA 疫苗为 59%,p=0.05)。在包括抗 CD20 患者的多变量分析中,阳性体液反应的预测因素是接受 mRNA 疫苗(OR 8.11(1.79-36.8),p=0.007)和总输注次数较少(OR 0.44(0.27-0.74),p=0.002)。最常见的 AESAV 是局部疼痛(14%),与首次接种后 8 周内 4 名(2.2%)患者出现轻度-中度复发相比,在接种疫苗前 8 周内 11 名(6.2%)患者出现复发(卡方 3.41,p=0.06)。

讨论

与灭活疫苗相比,使用 mRNA 观察到更高的体液反应率,而使用抗 CD20 的患者反应率明显较低,使用抗 CD20 和 fingolimod 的患者抗体滴度较低。在这一 MS 患者队列中,针对 SARS-CoV-2 的灭活疫苗和 mRNA 疫苗似乎是安全的,复发率没有增加。这些信息可能有助于指导方针,包括选定人群的加强针和疫苗类型。

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