Department of Physical Medicine & Rehabilitation, Larkin Community Hospital, South Miami, FL, USA.
St. Catherine's West Rehabilitation Hospital, Hialeah Gardens, FL, USA.
Am J Case Rep. 2022 Feb 14;23:e935275. doi: 10.12659/AJCR.935275.
BACKGROUND Since December 2020, multiple vaccines have mobilized mass immunization campaigns capable of mitigating the current SARS-COV-2 pandemic. Ad26.COV2.S (Johnson & Johnson/Janssen) is a recombinant, replication-incompetent vector vaccine encoding the SARS-CoV-2 spike (s) protein and is especially protective against severe-critical disease. It is a single-dose injection; adverse effects after vaccine administration are usually mild and self-limited, including pain at the injection site, headache, fatigue, muscle aches, and nausea. Severe adverse events involving hospitalization and death after Ad26.COV2.S rarely occur. However, not unlike previous viral vector vaccines, ongoing clinical trials may unveil rare complications of Ad26.COV2.S. Guillain-Barre Syndrome (GBS) is an autoimmune demyelinating polyneuropathy that can potentially manifest severe neurological symptoms after vaccination. CASE REPORT This report describes a case of classic GBS features that manifested 14 days after a single Ad26.COV2.S vaccine injection. The patient developed flaccid paralysis with treatment-related fluctuations. Our findings warrant further investigation into the potential relationship between SARS-CoV-2 vaccinations and the development of GBS. CONCLUSIONS A temporal association between the Ad26.COV2.S (Johnson & Johnson/Janssen) vaccine and the onset of GBS was demonstrated in this case report. A feasible underlying pathogenic mechanism involves the cross-reactivity of antibodies stimulated by adenovirus vaccine components and peripheral nerve glycoproteins. However, there is currently insufficient evidence to support a causal relationship between Ad26.COV2.S and the development of GBS. Further evidence gathered from clinician surveillance and clinical trials are needed to draw these conclusions.
自 2020 年 12 月以来,多种疫苗已开展大规模免疫接种活动,能够缓解当前的 SARS-CoV-2 大流行。Ad26.COV2.S(强生/杨森)是一种重组、复制缺陷型载体疫苗,编码 SARS-CoV-2 刺突(s)蛋白,对严重-危急疾病特别具有保护作用。它是一种单剂量注射剂;疫苗接种后的不良反应通常为轻度且自限性的,包括注射部位疼痛、头痛、疲劳、肌肉疼痛和恶心。Ad26.COV2.S 接种后涉及住院和死亡的严重不良事件很少发生。然而,与之前的病毒载体疫苗一样,正在进行的临床试验可能会揭示 Ad26.COV2.S 的罕见并发症。格林-巴利综合征(GBS)是一种自身免疫性脱髓鞘性多发性神经病,接种疫苗后可能会出现严重的神经系统症状。
本报告描述了一例在单次 Ad26.COV2.S 疫苗接种后 14 天出现典型 GBS 特征的病例。患者出现弛缓性瘫痪,与治疗相关波动。我们的发现证明需要进一步研究 SARS-CoV-2 疫苗接种与 GBS 发展之间的潜在关系。
本病例报告显示 Ad26.COV2.S(强生/杨森)疫苗与 GBS 的发病之间存在时间关联。一个可行的潜在发病机制涉及腺病毒疫苗成分和周围神经糖蛋白刺激的抗体的交叉反应。然而,目前尚无足够的证据支持 Ad26.COV2.S 与 GBS 发展之间存在因果关系。需要从临床医生监测和临床试验中收集更多证据来得出这些结论。