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

Ben MortonKayla G BarnesCatherine AnscombeKhuzwayo C JerePrisca MatamboJonathan MandoloRaphael Kamng'onaComfort BrownJames NyirendaTamara PhiriNdaziona P BandaCharlotte Van Der VeerKwazizira S MndoloKelvin MpondaJamie RylanceChimota PhiriJane MallewaMulinda NyirendaGrace KathaPaul KambiyaJames JafaliHenry C MwandumbaStephen B Gordonnull nullJennifer CornickKondwani C Jambo
Published in: Nature communications (2021)
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.
Keyphrases
  • coronavirus disease
  • sars cov
  • staphylococcus aureus
  • oxidative stress
  • ejection fraction
  • respiratory syndrome coronavirus
  • high dose
  • cystic fibrosis