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

Benjamin Morton, Kayla Barnes, Cat Anscombe, Khuzwayo Jere, Prisca Matambo, Jonathan Mandolo, Raphael Kamng’ona, Comfort Brown, James Nyirenda, Tamara Phiri, Ndaziona P. Banda, Charlotte Van Der Veer, Kwazizira S. Mndolo, Kelvin Mponda, Jamie Rylance, Chimota Phiri, Jane Mallewa, Mulinda Nyirenda, Grace Katha, Paul KambiyaJames Jafali, Henry Mwandumba, Stephen Gordon, Jennifer Cornick, Kondwani Jambo, Jacob Phulusa, Mercy Mkandawire, Sylvester Kaimba, Herbert Thole, Sharon Nthala, Edna Nsomba, Lucy Keyala, Peter Mandala, Beatrice Chinoko, Vella Kaudzu, Simon Sichone, Ajisa Ahmadu, Oscar Kanjewa, Vita Nyasulu, End Chinyama, Allan Zuza, Brigitte Denis, Chimwemwe Mhango, Agness Lakudzala, James Chirombo, Clemens Masesa, Peter MacPherson, Pui-Ying Iroh Tam, Leonard Mvaya, Marc Henrion

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

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.

Original languageEnglish
Article number3554
Pages (from-to)3554
JournalNature Communications
Volume12
Issue number1
DOIs
Publication statusPublished - 11 Jun 2021

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