SARS-CoV-2 induces human plasmacytoid predendritic cell diversification via UNC93B and IRAK4

J Exp Med. 2021 Apr 5;218(4):e20201387. doi: 10.1084/jem.20201387.

Abstract

Several studies have analyzed antiviral immune pathways in late-stage severe COVID-19. However, the initial steps of SARS-CoV-2 antiviral immunity are poorly understood. Here we have isolated primary SARS-CoV-2 viral strains and studied their interaction with human plasmacytoid predendritic cells (pDCs), a key player in antiviral immunity. We show that pDCs are not productively infected by SARS-CoV-2. However, they efficiently diversified into activated P1-, P2-, and P3-pDC effector subsets in response to viral stimulation. They expressed CD80, CD86, CCR7, and OX40 ligand at levels similar to influenza virus-induced activation. They rapidly produced high levels of interferon-α, interferon-λ1, IL-6, IP-10, and IL-8. All major aspects of SARS-CoV-2-induced pDC activation were inhibited by hydroxychloroquine. Mechanistically, SARS-CoV-2-induced pDC activation critically depended on IRAK4 and UNC93B1, as established using pDC from genetically deficient patients. Overall, our data indicate that human pDC are efficiently activated by SARS-CoV-2 particles and may thus contribute to type I IFN-dependent immunity against SARS-CoV-2 infection.

Publication types

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

MeSH terms

  • Biomarkers
  • COVID-19 / immunology*
  • COVID-19 / metabolism*
  • COVID-19 / virology
  • COVID-19 Drug Treatment
  • Cell Plasticity / immunology*
  • Cytokines / metabolism
  • Dendritic Cells / immunology*
  • Dendritic Cells / metabolism*
  • Dendritic Cells / virology
  • Host-Pathogen Interactions / immunology
  • Humans
  • Hydroxychloroquine / pharmacology
  • Hydroxychloroquine / therapeutic use
  • Immunomodulation
  • Immunophenotyping
  • Inflammation Mediators / metabolism
  • Interferon Lambda
  • Interferon Type I / metabolism
  • Interferons / metabolism
  • Interleukin-1 Receptor-Associated Kinases / metabolism*
  • Membrane Transport Proteins / metabolism*
  • SARS-CoV-2 / immunology*

Substances

  • Biomarkers
  • Cytokines
  • Inflammation Mediators
  • Interferon Type I
  • Membrane Transport Proteins
  • UNC93B1 protein, human
  • Hydroxychloroquine
  • Interferons
  • IRAK4 protein, human
  • Interleukin-1 Receptor-Associated Kinases
  • Interferon Lambda