Guillain–Barré Syndrome in COVID-19—The Potential Role of NCAM-1 and Immunotherapy

SPG biomed Pub Date : 2021-09-15 DOI:10.3390/biomed1010006
K. Laudanski, A. Yakhkind, Mariana Restrepo, Lindsay Draham, A. E. Lang
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引用次数: 4

Abstract

Coronavirus disease 2019 (COVID-19) interacts with the nervous system directly and indirectly by affecting the activation of the immune system. Guillain–Barré syndrome (GBS) is triggered by an inappropriate immune system activation that overlaps with the neurotoxic mechanism of an invading pathogen. Here, we discuss the complexity of an abnormal immune system response leading to the generation of autoimmunity in the setting of acute viral infection. A 67-year-old male patient with COVID-19 developed a sensory motor acute polyneuropathy with respiratory failure. Several serum inflammatory and neurodegeneration markers were collected during hospital days 1, 3, 8, and 67 and compared to healthy individuals. Neural cell adhesion molecule 1 (NCAM-1) and neurofilament light chain (NfL) values were highly variable when compared to healthy individuals, but not to the reference COVID-19 group. We focused our attention on NCAM-1 as a possible target for antibodies directed at COVID-19 in silico.
covid -19中的格林-巴利综合征- NCAM-1和免疫治疗的潜在作用
2019冠状病毒病(COVID-19)通过影响免疫系统的激活直接或间接地与神经系统相互作用。吉兰-巴罗综合征(GBS)是由不适当的免疫系统激活引发的,与入侵病原体的神经毒性机制重叠。在这里,我们讨论了在急性病毒感染的情况下导致自身免疫产生的异常免疫系统反应的复杂性。一名67岁男性COVID-19患者出现感觉运动急性多神经病变并呼吸衰竭。在住院第1、3、8和67天收集几种血清炎症和神经变性标志物,并与健康个体进行比较。与健康个体相比,神经细胞粘附分子1 (NCAM-1)和神经丝轻链(NfL)值变化很大,但与参考COVID-19组相比则没有变化。我们将注意力集中在NCAM-1上,作为针对COVID-19的芯片抗体的可能靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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