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Considering how biological sex impacts immune responses and COVID-19 outcomes

A male bias in mortality has emerged in the COVID-19 pandemic, which is consistent with the pathogenesis of other viral infections. Biological sex differences may manifest themselves in susceptibility to infection, early pathogenesis, innate viral control, adaptive immune responses or the balance of...

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Autores principales: Scully, Eileen P., Haverfield, Jenna, Ursin, Rebecca L., Tannenbaum, Cara, Klein, Sabra L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288618/
https://www.ncbi.nlm.nih.gov/pubmed/32528136
http://dx.doi.org/10.1038/s41577-020-0348-8
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author Scully, Eileen P.
Haverfield, Jenna
Ursin, Rebecca L.
Tannenbaum, Cara
Klein, Sabra L.
author_facet Scully, Eileen P.
Haverfield, Jenna
Ursin, Rebecca L.
Tannenbaum, Cara
Klein, Sabra L.
author_sort Scully, Eileen P.
collection PubMed
description A male bias in mortality has emerged in the COVID-19 pandemic, which is consistent with the pathogenesis of other viral infections. Biological sex differences may manifest themselves in susceptibility to infection, early pathogenesis, innate viral control, adaptive immune responses or the balance of inflammation and tissue repair in the resolution of infection. We discuss available sex-disaggregated epidemiological data from the COVID-19 pandemic, introduce sex-differential features of immunity and highlight potential sex differences underlying COVID-19 severity. We propose that sex differences in immunopathogenesis will inform mechanisms of COVID-19, identify points for therapeutic intervention and improve vaccine design and increase vaccine efficacy.
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spelling pubmed-72886182020-06-11 Considering how biological sex impacts immune responses and COVID-19 outcomes Scully, Eileen P. Haverfield, Jenna Ursin, Rebecca L. Tannenbaum, Cara Klein, Sabra L. Nat Rev Immunol Perspective A male bias in mortality has emerged in the COVID-19 pandemic, which is consistent with the pathogenesis of other viral infections. Biological sex differences may manifest themselves in susceptibility to infection, early pathogenesis, innate viral control, adaptive immune responses or the balance of inflammation and tissue repair in the resolution of infection. We discuss available sex-disaggregated epidemiological data from the COVID-19 pandemic, introduce sex-differential features of immunity and highlight potential sex differences underlying COVID-19 severity. We propose that sex differences in immunopathogenesis will inform mechanisms of COVID-19, identify points for therapeutic intervention and improve vaccine design and increase vaccine efficacy. Nature Publishing Group UK 2020-06-11 2020 /pmc/articles/PMC7288618/ /pubmed/32528136 http://dx.doi.org/10.1038/s41577-020-0348-8 Text en © Springer Nature Limited 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Perspective
Scully, Eileen P.
Haverfield, Jenna
Ursin, Rebecca L.
Tannenbaum, Cara
Klein, Sabra L.
Considering how biological sex impacts immune responses and COVID-19 outcomes
title Considering how biological sex impacts immune responses and COVID-19 outcomes
title_full Considering how biological sex impacts immune responses and COVID-19 outcomes
title_fullStr Considering how biological sex impacts immune responses and COVID-19 outcomes
title_full_unstemmed Considering how biological sex impacts immune responses and COVID-19 outcomes
title_short Considering how biological sex impacts immune responses and COVID-19 outcomes
title_sort considering how biological sex impacts immune responses and covid-19 outcomes
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288618/
https://www.ncbi.nlm.nih.gov/pubmed/32528136
http://dx.doi.org/10.1038/s41577-020-0348-8
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