Abstract

Bernardes et al. explore COVID-19 disease trajectories by performing longitudinal multi-omics analyses in peripheral blood samples from hospitalized patients. The analyses identify increased numbers of plasmablasts, interferon-activated megakaryocytes, and erythroid cells as hallmarks of severe disease and define molecular signatures linked to a fatal COVID-19 disease outcome.

Original languageEnglish
Pages (from-to)1296-1314.e9
JournalImmunity
Volume53
Issue number6
DOIs
StatePublished - 15 Dec 2020

Keywords

  • COVID-19
  • RNA-seq
  • acute respiratory distress
  • blood
  • disease trajectory
  • immune response
  • infectious disease
  • methylation
  • scRNA-seq
  • virus

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