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Distinct clinical and immunological profiles of patients with evidence of SARS-CoV-2 infection in sub-Saharan Africa

Although the COVID-19 pandemic has left no country untouched there has been limited research to understand clinical and immunological responses in African populations. Here we characterise patients hospitalised with suspected (PCR-negative/IgG-positive) or confirmed (PCR-positive) COVID-19, and heal...

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Autores principales: Morton, Ben, Barnes, Kayla G., Anscombe, Catherine, Jere, Khuzwayo, Matambo, Prisca, Mandolo, Jonathan, Kamng’ona, Raphael, Brown, Comfort, Nyirenda, James, Phiri, Tamara, Banda, Ndaziona P., Van Der Veer, Charlotte, Mndolo, Kwazizira S., Mponda, Kelvin, Rylance, Jamie, Phiri, Chimota, Mallewa, Jane, Nyirenda, Mulinda, Katha, Grace, Kambiya, Paul, Jafali, James, Mwandumba, Henry C., Gordon, Stephen B., Cornick, Jennifer, Jambo, Kondwani C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196064/
https://www.ncbi.nlm.nih.gov/pubmed/34117221
http://dx.doi.org/10.1038/s41467-021-23267-w
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author Morton, Ben
Barnes, Kayla G.
Anscombe, Catherine
Jere, Khuzwayo
Matambo, Prisca
Mandolo, Jonathan
Kamng’ona, Raphael
Brown, Comfort
Nyirenda, James
Phiri, Tamara
Banda, Ndaziona P.
Van Der Veer, Charlotte
Mndolo, Kwazizira S.
Mponda, Kelvin
Rylance, Jamie
Phiri, Chimota
Mallewa, Jane
Nyirenda, Mulinda
Katha, Grace
Kambiya, Paul
Jafali, James
Mwandumba, Henry C.
Gordon, Stephen B.
Cornick, Jennifer
Jambo, Kondwani C.
author_facet Morton, Ben
Barnes, Kayla G.
Anscombe, Catherine
Jere, Khuzwayo
Matambo, Prisca
Mandolo, Jonathan
Kamng’ona, Raphael
Brown, Comfort
Nyirenda, James
Phiri, Tamara
Banda, Ndaziona P.
Van Der Veer, Charlotte
Mndolo, Kwazizira S.
Mponda, Kelvin
Rylance, Jamie
Phiri, Chimota
Mallewa, Jane
Nyirenda, Mulinda
Katha, Grace
Kambiya, Paul
Jafali, James
Mwandumba, Henry C.
Gordon, Stephen B.
Cornick, Jennifer
Jambo, Kondwani C.
author_sort Morton, Ben
collection PubMed
description Although the COVID-19 pandemic has left no country untouched there has been limited research to understand clinical and immunological responses in African populations. Here we characterise patients hospitalised with suspected (PCR-negative/IgG-positive) or confirmed (PCR-positive) COVID-19, and healthy community controls (PCR-negative/IgG-negative). PCR-positive COVID-19 participants were more likely to receive dexamethasone and a beta-lactam antibiotic, and survive to hospital discharge than PCR-negative/IgG-positive and PCR-negative/IgG-negative participants. PCR-negative/IgG-positive participants exhibited a nasal and systemic cytokine signature analogous to PCR-positive COVID-19 participants, predominated by chemokines and neutrophils and distinct from PCR-negative/IgG-negative participants. PCR-negative/IgG-positive participants had increased propensity for Staphylococcus aureus and Streptococcus pneumoniae colonisation. PCR-negative/IgG-positive individuals with high COVID-19 clinical suspicion had inflammatory profiles analogous to PCR-confirmed disease and potentially represent a target population for COVID-19 treatment strategies.
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spelling pubmed-81960642021-06-17 Distinct clinical and immunological profiles of patients with evidence of SARS-CoV-2 infection in sub-Saharan Africa Morton, Ben Barnes, Kayla G. Anscombe, Catherine Jere, Khuzwayo Matambo, Prisca Mandolo, Jonathan Kamng’ona, Raphael Brown, Comfort Nyirenda, James Phiri, Tamara Banda, Ndaziona P. Van Der Veer, Charlotte Mndolo, Kwazizira S. Mponda, Kelvin Rylance, Jamie Phiri, Chimota Mallewa, Jane Nyirenda, Mulinda Katha, Grace Kambiya, Paul Jafali, James Mwandumba, Henry C. Gordon, Stephen B. Cornick, Jennifer Jambo, Kondwani C. Nat Commun Article Although the COVID-19 pandemic has left no country untouched there has been limited research to understand clinical and immunological responses in African populations. Here we characterise patients hospitalised with suspected (PCR-negative/IgG-positive) or confirmed (PCR-positive) COVID-19, and healthy community controls (PCR-negative/IgG-negative). PCR-positive COVID-19 participants were more likely to receive dexamethasone and a beta-lactam antibiotic, and survive to hospital discharge than PCR-negative/IgG-positive and PCR-negative/IgG-negative participants. PCR-negative/IgG-positive participants exhibited a nasal and systemic cytokine signature analogous to PCR-positive COVID-19 participants, predominated by chemokines and neutrophils and distinct from PCR-negative/IgG-negative participants. PCR-negative/IgG-positive participants had increased propensity for Staphylococcus aureus and Streptococcus pneumoniae colonisation. PCR-negative/IgG-positive individuals with high COVID-19 clinical suspicion had inflammatory profiles analogous to PCR-confirmed disease and potentially represent a target population for COVID-19 treatment strategies. Nature Publishing Group UK 2021-06-11 /pmc/articles/PMC8196064/ /pubmed/34117221 http://dx.doi.org/10.1038/s41467-021-23267-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Morton, Ben
Barnes, Kayla G.
Anscombe, Catherine
Jere, Khuzwayo
Matambo, Prisca
Mandolo, Jonathan
Kamng’ona, Raphael
Brown, Comfort
Nyirenda, James
Phiri, Tamara
Banda, Ndaziona P.
Van Der Veer, Charlotte
Mndolo, Kwazizira S.
Mponda, Kelvin
Rylance, Jamie
Phiri, Chimota
Mallewa, Jane
Nyirenda, Mulinda
Katha, Grace
Kambiya, Paul
Jafali, James
Mwandumba, Henry C.
Gordon, Stephen B.
Cornick, Jennifer
Jambo, Kondwani C.
Distinct clinical and immunological profiles of patients with evidence of SARS-CoV-2 infection in sub-Saharan Africa
title Distinct clinical and immunological profiles of patients with evidence of SARS-CoV-2 infection in sub-Saharan Africa
title_full Distinct clinical and immunological profiles of patients with evidence of SARS-CoV-2 infection in sub-Saharan Africa
title_fullStr Distinct clinical and immunological profiles of patients with evidence of SARS-CoV-2 infection in sub-Saharan Africa
title_full_unstemmed Distinct clinical and immunological profiles of patients with evidence of SARS-CoV-2 infection in sub-Saharan Africa
title_short Distinct clinical and immunological profiles of patients with evidence of SARS-CoV-2 infection in sub-Saharan Africa
title_sort distinct clinical and immunological profiles of patients with evidence of sars-cov-2 infection in sub-saharan africa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196064/
https://www.ncbi.nlm.nih.gov/pubmed/34117221
http://dx.doi.org/10.1038/s41467-021-23267-w
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