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Nat Commun ; 12(1): 3554, 2021 06 11.
Article in English | MEDLINE | ID: mdl-34117221

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.


Subject(s)
COVID-19/immunology , Adult , Africa South of the Sahara/epidemiology , Anti-Bacterial Agents/administration & dosage , Antibodies/blood , COVID-19/blood , COVID-19/epidemiology , Coinfection/immunology , Cytokines/blood , Dexamethasone/administration & dosage , Female , Humans , Immunoglobulin G/blood , Immunoglobulin M/blood , Male , Middle Aged , Pandemics , SARS-CoV-2/isolation & purification , COVID-19 Drug Treatment
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