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接种 SARS-CoV-2 疫苗后的神经自身免疫性疾病:病例系列研究。

Neurological autoimmune diseases following vaccinations against SARS-CoV-2: a case series.

机构信息

Department of Neurology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.

Department of Neuroradiology, University Hospital Heidelberg, Heidelberg University, Heidelberg, Germany.

出版信息

Eur J Neurol. 2022 Feb;29(2):555-563. doi: 10.1111/ene.15147. Epub 2021 Oct 31.

Abstract

BACKGROUND AND PURPOSE

Population-based studies suggest that severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines may trigger immune-mediated thrombotic thrombocytopenia (VITT) raising concerns for other autoimmune responses. The aim was to characterize neurological autoimmunity after SARS-CoV-2 vaccinations.

METHODS

In this single-centre prospective case study patients with neurological autoimmunity in temporal association (≤6 weeks) with SARS-CoV-2 vaccinations and without other triggers are reported. Clinical, laboratory and imaging data were collected with a median follow-up of 49 days.

RESULTS

In the study period 232,603 inhabitants from the main catchment area of our hospital (Rhein-Neckar-Kreis, county) received SARS-CoV-2 vaccinations. Twenty-one cases (new onset n = 17, flares n = 4) diagnosed a median of 11 days (range 3-23) following SARS-CoV-2 vaccinations (BNT162b2 n = 12, ChAdOx1 n = 8, mRNA-1273 n = 1) were identified. Cases included VITT with cerebral venous sinus thrombosis (n = 3), central nervous system demyelinating diseases (n = 8), inflammatory peripheral neuropathies (n = 4), myositis (n = 3), myasthenia (n = 1), limbic encephalitis (n = 1) and giant cell arteritis (n = 1). Patients were predominantly female (ratio 3.2:1) and the median age at diagnosis was 50 years (range 22-86). Therapy included administration of steroids (n = 15), intravenous immunoglobulins in patients with Guillain-Barré syndrome or VITT (n = 4), plasma exchange in cases unresponsive to steroids (n = 3) and anticoagulation in VITT. Outcomes were favourable with partial and complete remissions achieved in 71% and 24%, respectively. Two patients received their second vaccination without further aggravation of autoimmune symptoms under low-dose immunosuppressants.

CONCLUSIONS

In this study various neurological autoimmune disorders encountered following SARS-CoV-2 vaccinations are characterized. Given the assumed low incidence and mostly favourable outcome of autoimmune responses, the benefits of vaccinations outweigh the comparatively small risks.

摘要

背景与目的

基于人群的研究表明,严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)疫苗可能引发免疫介导的血栓性血小板减少症(VITT),从而引发对其他自身免疫反应的担忧。本研究旨在描述 SARS-CoV-2 疫苗接种后的神经自身免疫情况。

方法

本研究为单中心前瞻性病例研究,报道了与 SARS-CoV-2 疫苗接种在时间上有明确关联(≤6 周)且无其他诱因的患者发生神经自身免疫性疾病的情况。收集了患者的临床、实验室和影像学数据,中位随访时间为 49 天。

结果

在研究期间,我院(莱茵-内卡县)主要收治区的 232603 名居民接种了 SARS-CoV-2 疫苗。接种 SARS-CoV-2 疫苗后中位数 11 天(范围 3-23 天)确诊 21 例(新发病例 n=17,复发 n=4),分别使用了 BNT162b2(n=12)、ChAdOx1(n=8)和 mRNA-1273(n=1)。这些病例包括伴有脑静脉窦血栓形成的 VITT(n=3)、中枢神经系统脱髓鞘疾病(n=8)、炎症性周围神经病(n=4)、肌炎(n=3)、重症肌无力(n=1)、边缘叶脑炎(n=1)和巨细胞动脉炎(n=1)。患者以女性为主(男女比为 3.2:1),中位发病年龄为 50 岁(范围 22-86 岁)。治疗方案包括使用类固醇(n=15)、静脉注射免疫球蛋白治疗吉兰-巴雷综合征或 VITT(n=4)、对类固醇无反应的病例采用血浆置换(n=3)以及 VITT 患者采用抗凝治疗。71%的患者取得部分缓解,24%的患者取得完全缓解,预后良好。2 例患者在低剂量免疫抑制剂治疗下接受第二次疫苗接种,自身免疫症状无加重。

结论

本研究对 SARS-CoV-2 疫苗接种后出现的各种神经自身免疫性疾病进行了特征描述。鉴于自身免疫反应的假定低发生率和大多良好的预后,疫苗接种的益处超过了相对较小的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4f5/8652629/7fb3cf821d15/ENE-29-555-g002.jpg

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