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Dysregulation of Protein S in COVID-19

Coronavirus Disease 2019 (COVID-19) has been widely associated with increased thrombotic risk, with many different proposed mechanisms. One such mechanism is acquired deficiency of protein S (PS), a plasma protein that regulates coagulation and inflammatory processes, including complement activation...

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Detalles Bibliográficos
Autores principales: Sim, Martha M.S., Wood, Jeremy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395234/
https://www.ncbi.nlm.nih.gov/pubmed/36494145
http://dx.doi.org/10.1016/j.beha.2022.101376
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author Sim, Martha M.S.
Wood, Jeremy P.
author_facet Sim, Martha M.S.
Wood, Jeremy P.
author_sort Sim, Martha M.S.
collection PubMed
description Coronavirus Disease 2019 (COVID-19) has been widely associated with increased thrombotic risk, with many different proposed mechanisms. One such mechanism is acquired deficiency of protein S (PS), a plasma protein that regulates coagulation and inflammatory processes, including complement activation and efferocytosis. Acquired PS deficiency is common in patients with severe viral infections and has been reported in multiple studies of COVID-19. This deficiency may be caused by consumption, degradation, or clearance of the protein, by decreased synthesis, or by binding of PS to other plasma proteins, which block its anticoagulant activity. Here, we review the functions of PS, the evidence of acquired PS deficiency in COVID-19 patients, the potential mechanisms of PS deficiency, and the evidence that those mechanisms may be occurring in COVID-19.
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spelling pubmed-93952342022-08-23 Dysregulation of Protein S in COVID-19 Sim, Martha M.S. Wood, Jeremy P. Best Pract Res Clin Haematol Article Coronavirus Disease 2019 (COVID-19) has been widely associated with increased thrombotic risk, with many different proposed mechanisms. One such mechanism is acquired deficiency of protein S (PS), a plasma protein that regulates coagulation and inflammatory processes, including complement activation and efferocytosis. Acquired PS deficiency is common in patients with severe viral infections and has been reported in multiple studies of COVID-19. This deficiency may be caused by consumption, degradation, or clearance of the protein, by decreased synthesis, or by binding of PS to other plasma proteins, which block its anticoagulant activity. Here, we review the functions of PS, the evidence of acquired PS deficiency in COVID-19 patients, the potential mechanisms of PS deficiency, and the evidence that those mechanisms may be occurring in COVID-19. Elsevier Ltd. 2022-09 2022-08-23 /pmc/articles/PMC9395234/ /pubmed/36494145 http://dx.doi.org/10.1016/j.beha.2022.101376 Text en © 2022 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Sim, Martha M.S.
Wood, Jeremy P.
Dysregulation of Protein S in COVID-19
title Dysregulation of Protein S in COVID-19
title_full Dysregulation of Protein S in COVID-19
title_fullStr Dysregulation of Protein S in COVID-19
title_full_unstemmed Dysregulation of Protein S in COVID-19
title_short Dysregulation of Protein S in COVID-19
title_sort dysregulation of protein s in covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395234/
https://www.ncbi.nlm.nih.gov/pubmed/36494145
http://dx.doi.org/10.1016/j.beha.2022.101376
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