Systems biological assessment of immunity to mild versus severe COVID-19 infection in humans

Science. 2020 Sep 4;369(6508):1210-1220. doi: 10.1126/science.abc6261. Epub 2020 Aug 11.

Abstract

Coronavirus disease 2019 (COVID-19) represents a global crisis, yet major knowledge gaps remain about human immunity to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). We analyzed immune responses in 76 COVID-19 patients and 69 healthy individuals from Hong Kong and Atlanta, Georgia, United States. In the peripheral blood mononuclear cells (PBMCs) of COVID-19 patients, we observed reduced expression of human leukocyte antigen class DR (HLA-DR) and proinflammatory cytokines by myeloid cells as well as impaired mammalian target of rapamycin (mTOR) signaling and interferon-α (IFN-α) production by plasmacytoid dendritic cells. By contrast, we detected enhanced plasma levels of inflammatory mediators-including EN-RAGE, TNFSF14, and oncostatin M-which correlated with disease severity and increased bacterial products in plasma. Single-cell transcriptomics revealed a lack of type I IFNs, reduced HLA-DR in the myeloid cells of patients with severe COVID-19, and transient expression of IFN-stimulated genes. This was consistent with bulk PBMC transcriptomics and transient, low IFN-α levels in plasma during infection. These results reveal mechanisms and potential therapeutic targets for COVID-19.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Betacoronavirus / immunology*
  • COVID-19
  • Coronavirus Infections / immunology*
  • Cytokines / blood
  • DNA, Bacterial / blood
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism
  • Female
  • Flow Cytometry
  • HLA-DR Antigens / analysis
  • Humans
  • Immunity
  • Immunity, Innate
  • Immunoglobulins / blood
  • Immunoglobulins / immunology
  • Inflammation Mediators / blood
  • Interferon Type I / metabolism
  • Leukocytes, Mononuclear / immunology
  • Leukocytes, Mononuclear / metabolism
  • Lipopolysaccharides / blood
  • Male
  • Myeloid Cells / immunology
  • Myeloid Cells / metabolism
  • Pandemics
  • Pneumonia, Viral / immunology*
  • SARS-CoV-2
  • Signal Transduction
  • Single-Cell Analysis
  • Systems Biology
  • TOR Serine-Threonine Kinases / metabolism
  • Transcription, Genetic
  • Transcriptome

Substances

  • Cytokines
  • DNA, Bacterial
  • HLA-DR Antigens
  • Immunoglobulins
  • Inflammation Mediators
  • Interferon Type I
  • Lipopolysaccharides
  • MTOR protein, human
  • TOR Serine-Threonine Kinases