Ballout Ahmad A, Babaie Anna, Kolesnik Michael, Li Jian Yi, Hameed Natasha, Waldman Glenn, Chaudhry Frasat, Saba Sami, Harel Asaff, Najjar Souhel
Department of Neurology, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, United States.
Pathology, Northwell Health, Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY, United States.
Front Neurol. 2022 Feb 24;13:796882. doi: 10.3389/fneur.2022.796882. eCollection 2022.
Since 2020, over 250 million doses of mRNA-based SARS-CoV-2 vaccines have been administered in the United States and hundreds of millions worldwide between the Pfizer-BioNTech and Moderna SARS-CoV-2 vaccines. To date, there have been rare reports associating mRNA-based SARS-CoV-2 vaccines with episodes of inflammatory and autoimmune CNS disorders. We report a case series of five patients with new-onset neurological disorders of inflammatory or immunological origin temporally associated with these vaccines.
A case-series of five patients within a single 23-hospital health system who developed new-onset CNS inflammatory disease within 2 weeks of receiving a dose of an mRNA-based SARS-CoV-2 vaccine.
Five cases of post-vaccination CNS disorders of immune origin (fatal ADEM; = 1, new-onset NMOSD; = 2, new-clinical onset MS-like syndrome but with preexisting clinically silent mild demyelination; = 1, meningoencephalitis; = 1) observed within 2 weeks of inoculation with either the first or second dose of mRNA-based SARS-CoV-2 vaccines (Moderna = 3, Pfizer = 2).
To our knowledge, these are among the emerging cases of CNS adverse events of immunological or inflammatory origin. These findings should be interpreted with great caution as they neither prove a mechanistic link nor imply a potential long-term increased risk in post-vaccination CNS autoimmunity. Larger prospective studies assessing the potential association between mRNA-based vaccination and the development of neurological adverse events of suspected immune origin, particularly among those with underlying CNS or systemic autoimmune disorders, are needed. The use of mRNA-based SARS-CoV-2 vaccines should continue to be strongly encouraged given their high efficacy in overcoming this pandemic.
自2020年以来,美国已接种超过2.5亿剂基于mRNA的新冠病毒疫苗,辉瑞-生物科技公司和莫德纳公司的新冠病毒疫苗在全球接种了数亿剂。迄今为止,仅有罕见报告将基于mRNA的新冠病毒疫苗与炎症性和自身免疫性中枢神经系统疾病发作相关联。我们报告了一系列五例患者,他们出现了与这些疫苗在时间上相关的、新发性的炎症或免疫性起源的神经系统疾病。
在一个由23家医院组成的医疗系统中,对五例在接种一剂基于mRNA的新冠病毒疫苗后2周内出现新发中枢神经系统炎症性疾病的患者进行病例系列研究。
在接种第一剂或第二剂基于mRNA的新冠病毒疫苗(莫德纳疫苗 = 3例,辉瑞疫苗 = 2例)后2周内,观察到五例免疫起源的疫苗接种后中枢神经系统疾病(致死性急性播散性脑脊髓炎;1例,新发视神经脊髓炎谱系障碍;2例,新临床发作的类似多发性硬化综合征但先前存在临床无症状的轻度脱髓鞘;1例,脑膜脑炎;1例)。
据我们所知,这些是免疫或炎症起源的中枢神经系统不良事件的新出现病例。这些发现应极为谨慎地解读,因为它们既未证明存在机制联系,也未暗示疫苗接种后中枢神经系统自身免疫存在潜在的长期风险增加。需要开展更大规模的前瞻性研究,以评估基于mRNA的疫苗接种与疑似免疫起源的神经系统不良事件发生之间的潜在关联,特别是在那些患有潜在中枢神经系统或全身性自身免疫性疾病的人群中。鉴于基于mRNA的新冠病毒疫苗在战胜这一疫情方面具有高效性,应继续大力鼓励使用此类疫苗。