Cheng Mei-Yun, Ho Hsuan-Chen, Hsu Jung-Lung, Wang Yi, Chen Linyi, Lim Siew-Na, Liao Ming-Feng, Ro Long-Sun
Section of Epilepsy, Department of Neurology, Chang Gung Memorial Hospital at Linkou Medical Center and Chang Gung University College of Medicine, Taoyuan 333, Taiwan.
Department of Medical Science, National Tsing Hua University, Hsinchu 300, Taiwan.
Diseases. 2024 Mar 20;12(3):60. doi: 10.3390/diseases12030060.
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.
针对新冠疫情已研发出多种疫苗,疫苗安全性成为重要问题。近期有新冠疫苗相关的中枢神经系统炎性脱髓鞘疾病(CNS IDDs)的报道。我们报告1例与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月发表的另外78例患者进行文献综述。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例与新冠疫苗相关的CNS IDDs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%)确诊有自身抗体,其中15例(19%)有抗MOG抗体,11例(13.9%)有抗水通道蛋白4(AQP4)抗体,1例(1.3%)两种抗体都有。值得注意的是,与mRNA疫苗和灭活疫苗相比,接种病毒载体疫苗后发生CNS IDDs的男性更多。接种mRNA疫苗的患者比接种其他类型疫苗的患者年龄更大。此外,mRNA疫苗和灭活疫苗与抗AQP4抗体的相关性更高,而病毒载体疫苗的MOG阳性率更高。本研究表明,新冠疫苗相关的CNS IDDs与性别、年龄和自身抗体之间可能存在关联,具体取决于疫苗类型。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CNS IDDs的机制,有助于特定类型疫苗的选择。