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Molecular mimicry of NMDA receptors may contribute to neuropsychiatric symptoms in severe COVID-19 cases

Approximately 30% of individuals with severe SARS-CoV-2 infections also develop neurological and psychiatric complaints. In rare cases, the occurrence of autoimmune encephalitis has been reported after SARS-CoV-2 infection. In this systematic review, we have identified eight SARS-CoV-2-associated ca...

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Autores principales: Vasilevska, Veronika, Guest, Paul C., Bernstein, Hans-Gert, Schroeter, Matthias L., Geis, Christian, Steiner, Johann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551937/
https://www.ncbi.nlm.nih.gov/pubmed/34711233
http://dx.doi.org/10.1186/s12974-021-02293-x
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author Vasilevska, Veronika
Guest, Paul C.
Bernstein, Hans-Gert
Schroeter, Matthias L.
Geis, Christian
Steiner, Johann
author_facet Vasilevska, Veronika
Guest, Paul C.
Bernstein, Hans-Gert
Schroeter, Matthias L.
Geis, Christian
Steiner, Johann
author_sort Vasilevska, Veronika
collection PubMed
description Approximately 30% of individuals with severe SARS-CoV-2 infections also develop neurological and psychiatric complaints. In rare cases, the occurrence of autoimmune encephalitis has been reported after SARS-CoV-2 infection. In this systematic review, we have identified eight SARS-CoV-2-associated cases of anti-NMDA receptor encephalitis. All had cerebrospinal fluid antibodies against the NMDA receptor and a recent onset of working memory deficits, altered mental status, or psychiatric symptoms, such as confusion, agitation, auditory hallucination, catatonia and speech dysfunction. All patients received high-dose steroid and immunoglobulin therapeutics and conditions improved in each case. These findings suggest that clinical attention should be paid to warning signs of autoimmune encephalitis in severe COVID-19 cases. If characteristic features of autoimmune encephalitis are present, autoantibody diagnostics should be performed and confirmed cases should be treated with immunotherapy to minimize neurological impairments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-021-02293-x.
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spelling pubmed-85519372021-10-28 Molecular mimicry of NMDA receptors may contribute to neuropsychiatric symptoms in severe COVID-19 cases Vasilevska, Veronika Guest, Paul C. Bernstein, Hans-Gert Schroeter, Matthias L. Geis, Christian Steiner, Johann J Neuroinflammation Review Approximately 30% of individuals with severe SARS-CoV-2 infections also develop neurological and psychiatric complaints. In rare cases, the occurrence of autoimmune encephalitis has been reported after SARS-CoV-2 infection. In this systematic review, we have identified eight SARS-CoV-2-associated cases of anti-NMDA receptor encephalitis. All had cerebrospinal fluid antibodies against the NMDA receptor and a recent onset of working memory deficits, altered mental status, or psychiatric symptoms, such as confusion, agitation, auditory hallucination, catatonia and speech dysfunction. All patients received high-dose steroid and immunoglobulin therapeutics and conditions improved in each case. These findings suggest that clinical attention should be paid to warning signs of autoimmune encephalitis in severe COVID-19 cases. If characteristic features of autoimmune encephalitis are present, autoantibody diagnostics should be performed and confirmed cases should be treated with immunotherapy to minimize neurological impairments. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-021-02293-x. BioMed Central 2021-10-28 /pmc/articles/PMC8551937/ /pubmed/34711233 http://dx.doi.org/10.1186/s12974-021-02293-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Vasilevska, Veronika
Guest, Paul C.
Bernstein, Hans-Gert
Schroeter, Matthias L.
Geis, Christian
Steiner, Johann
Molecular mimicry of NMDA receptors may contribute to neuropsychiatric symptoms in severe COVID-19 cases
title Molecular mimicry of NMDA receptors may contribute to neuropsychiatric symptoms in severe COVID-19 cases
title_full Molecular mimicry of NMDA receptors may contribute to neuropsychiatric symptoms in severe COVID-19 cases
title_fullStr Molecular mimicry of NMDA receptors may contribute to neuropsychiatric symptoms in severe COVID-19 cases
title_full_unstemmed Molecular mimicry of NMDA receptors may contribute to neuropsychiatric symptoms in severe COVID-19 cases
title_short Molecular mimicry of NMDA receptors may contribute to neuropsychiatric symptoms in severe COVID-19 cases
title_sort molecular mimicry of nmda receptors may contribute to neuropsychiatric symptoms in severe covid-19 cases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551937/
https://www.ncbi.nlm.nih.gov/pubmed/34711233
http://dx.doi.org/10.1186/s12974-021-02293-x
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