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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.
  • Morton B; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi. ben.morton@lstmed.ac.uk.
  • Barnes KG; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK. ben.morton@lstmed.ac.uk.
  • Anscombe C; Liverpool University Hospitals NHS Foundation Trust, Liverpool, UK. ben.morton@lstmed.ac.uk.
  • Jere K; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Matambo P; Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
  • Mandolo J; Harvard School of Public Health, Boston, MA, USA.
  • Kamng'ona R; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Brown C; University of Glasgow MRC Centre for Virus Research, Glasgow, UK.
  • Nyirenda J; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Phiri T; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
  • Banda NP; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Van Der Veer C; Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
  • Mndolo KS; University of Malawi-College of Medicine, Blantyre, Malawi.
  • Mponda K; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Rylance J; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Phiri C; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Mallewa J; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Nyirenda M; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Katha G; Department of Medicine, Queen Elizabeth Central Hospital, Blantyre, Malawi.
  • Kambiya P; University of Malawi-College of Medicine, Blantyre, Malawi.
  • Jafali J; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Mwandumba HC; Institute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Liverpool, UK.
  • Gordon SB; Department of Medicine, Queen Elizabeth Central Hospital, Blantyre, Malawi.
  • Cornick J; Malawi-Liverpool-Wellcome Trust Clinical Research Programme, University of Malawi College of Medicine, Blantyre, Malawi.
  • Jambo KC; Department of Clinical Sciences, Liverpool School of Tropical Medicine, Liverpool, UK.
Nat Commun ; 12(1): 3554, 2021 06 11.
Article in English | MEDLINE | ID: covidwho-1265949
ABSTRACT
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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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Observational study / Prognostic study Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2021 Document Type: Article Affiliation country: S41467-021-23267-w

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Observational study / Prognostic study Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: Africa Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2021 Document Type: Article Affiliation country: S41467-021-23267-w