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How should we use convalescent plasma therapies for the management of COVID-19?

Convalescent plasma (CP) from blood donors with antibodies to severe acute respiratory syndrome coronavirus 2 may benefit patients with COVID-19 by providing immediate passive immunity via transfusion or by being used to manufacture hyperimmune immunoglobulin preparations. Optimal product characteri...

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Detalles Bibliográficos
Autores principales: Wood, Erica M., Estcourt, Lise J., McQuilten, Zoe K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992504/
https://www.ncbi.nlm.nih.gov/pubmed/33202419
http://dx.doi.org/10.1182/blood.2020008903
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author Wood, Erica M.
Estcourt, Lise J.
McQuilten, Zoe K.
author_facet Wood, Erica M.
Estcourt, Lise J.
McQuilten, Zoe K.
author_sort Wood, Erica M.
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description Convalescent plasma (CP) from blood donors with antibodies to severe acute respiratory syndrome coronavirus 2 may benefit patients with COVID-19 by providing immediate passive immunity via transfusion or by being used to manufacture hyperimmune immunoglobulin preparations. Optimal product characteristics (including neutralizing antibody titers), transfusion volume, and administration timing remain to be determined. Preliminary COVID-19 CP safety data are encouraging, but establishing the clinical efficacy of CP requires an ongoing international collaborative effort. Preliminary results from large, high-quality randomized trials have recently started to be reported.
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spelling pubmed-79925042021-03-26 How should we use convalescent plasma therapies for the management of COVID-19? Wood, Erica M. Estcourt, Lise J. McQuilten, Zoe K. Blood BLOOD Spotlight Convalescent plasma (CP) from blood donors with antibodies to severe acute respiratory syndrome coronavirus 2 may benefit patients with COVID-19 by providing immediate passive immunity via transfusion or by being used to manufacture hyperimmune immunoglobulin preparations. Optimal product characteristics (including neutralizing antibody titers), transfusion volume, and administration timing remain to be determined. Preliminary COVID-19 CP safety data are encouraging, but establishing the clinical efficacy of CP requires an ongoing international collaborative effort. Preliminary results from large, high-quality randomized trials have recently started to be reported. American Society of Hematology 2021-03-25 /pmc/articles/PMC7992504/ /pubmed/33202419 http://dx.doi.org/10.1182/blood.2020008903 Text en © 2021 by The American Society of Hematology
spellingShingle BLOOD Spotlight
Wood, Erica M.
Estcourt, Lise J.
McQuilten, Zoe K.
How should we use convalescent plasma therapies for the management of COVID-19?
title How should we use convalescent plasma therapies for the management of COVID-19?
title_full How should we use convalescent plasma therapies for the management of COVID-19?
title_fullStr How should we use convalescent plasma therapies for the management of COVID-19?
title_full_unstemmed How should we use convalescent plasma therapies for the management of COVID-19?
title_short How should we use convalescent plasma therapies for the management of COVID-19?
title_sort how should we use convalescent plasma therapies for the management of covid-19?
topic BLOOD Spotlight
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992504/
https://www.ncbi.nlm.nih.gov/pubmed/33202419
http://dx.doi.org/10.1182/blood.2020008903
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