与 COVID-19 疫苗相关的中枢神经系统炎症性脱髓鞘疾病的临床研究

Diseases Pub Date : 2024-03-20 DOI:10.3390/diseases12030060
Mei-Yun Cheng, Hsuan-Chen Ho, Jung-Lung Hsu, Yi Wang, Linyi Chen, Siew-Na Lim, M. Liao, Long-Sun Ro
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摘要

为应对 SARS-CoV-2 大流行,人们开发了各种疫苗,疫苗的安全性已成为一个重要问题。最近有报道称,与 COVID-19 疫苗相关的中枢神经系统炎症性脱髓鞘疾病(CNS IDDs)也有发生。我们介绍了一例阿斯利康疫苗相关的髓鞘少突胶质细胞糖蛋白(MOG)抗体相关疾病,并对2020年1月至2022年10月期间发表的另外78例患者进行了文献回顾。患者被分为三种疫苗类型(病毒载体疫苗、mRNA疫苗和灭活疫苗)进行进一步分析。在79例COVID-19疫苗相关中枢神经系统IDD患者中,49例(62%)接种了病毒载体疫苗,20例(25.3%)接种了mRNA疫苗,10例(12.7%)接种了灭活疫苗。27例(34.2%)患者确诊存在自身抗体,其中15例(19%)患者存在抗MOG抗体,11例(13.9%)患者存在抗喹诺酮4(AQP4)抗体,1例(1.3%)患者同时存在两种抗体。值得注意的是,与 mRNA 和灭活疫苗相比,接种病毒载体疫苗后出现中枢神经系统 IDD 的男性患者更多。接种 mRNA 疫苗的患者年龄比接种其他类型疫苗的患者大。此外,mRNA 和灭活疫苗与抗 AQP4 抗体的相关性更高,而病毒载体疫苗的 MOG 阳性率更高。这项研究表明,COVID-19 疫苗相关的中枢神经系统 IDD 与性别、年龄和自身抗体之间可能存在关联,这取决于疫苗类型。蛋白质序列分析表明,S 蛋白与 AQP4/MOG 之间存在相似性。进一步的研究可能会阐明中枢神经系统 IDD 的机制,从而帮助选择特定类型的疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Research into Central Nervous System Inflammatory Demyelinating Diseases Related to COVID-19 Vaccines
Various vaccines have been developed in response to the SARS-CoV-2 pandemic, and the safety of vaccines has become an important issue. COVID-19 vaccine-related central nervous system inflammatory demyelinating diseases (CNS IDDs) have been reported recently. We present one case of AstraZeneca vaccine-related myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease and a literature review of another 78 patients published from January 2020 to October 2022. Patients were divided into three vaccine types (viral vector, mRNA, and inactivated vaccines) for further analyses. Among 79 patients with COVID-19 vaccine-related CNS IDDs, 49 (62%) cases received viral vector vaccines, 20 (25.3%) received mRNA vaccines, and 10 (12.7%) received inactivated vaccines. Twenty-seven cases (34.2%) were confirmed with autoantibodies, including fifteen patients (19%) with anti-MOG, eleven (13.9%) with anti-aquaporin 4 (AQP4), and one (1.3%) with both antibodies. Significantly, more males developed CNS IDDs post viral vector vaccines compared to mRNA and inactivated vaccines. Patients receiving mRNA vaccines were older than those receiving other types. Furthermore, mRNA and inactivated vaccines correlated more with anti-AQP4 antibodies, while viral vector vaccines showed higher MOG positivity. This research suggests potential associations between COVID-19 vaccine-related CNS IDDs and gender, age, and autoantibodies, contingent on vaccine types. Protein sequence analysis implies similarities between the S protein and AQP4/MOG. Further studies may elucidate the mechanisms of CNS IDDs, aiding vaccine selection for specific types.
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