Dysregulation of Pulmonary Responses in Severe COVID-19

Viruses. 2021 May 21;13(6):957. doi: 10.3390/v13060957.

Abstract

Patients with coronavirus disease 2019 (COVID-19) predominantly have a respiratory tract infection with various symptoms and high mortality is associated with respiratory failure second to severe disease. The risk factors leading to severe disease remain unclear. Here, we reanalyzed a published single-cell RNA-Seq (scRNA-Seq) dataset and found that bronchoalveolar lavage fluid (BALF) of patients with severe disease compared to those with mild disease contained decreased TH17-type cells, decreased IFNA1-expressing cells with lower expression of toll-like receptor 7 (TLR7) and TLR8, increased IgA-expressing B cells, and increased hyperactive epithelial cells (and/or macrophages) expressing matrix metalloproteinases (MMPs), hyaluronan synthase 2 (HAS2), and plasminogen activator inhibitor-1 (PAI-1), which may together contribute to the pulmonary pathology in severe COVID-19. We propose IFN-I (and TLR7/TLR8) and PAI-1 as potential biomarkers to predict the susceptibility to severe COVID-19.

Keywords: COVID-19; IgA; PAI-1; TH17; type I interferon.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • B-Lymphocytes / metabolism
  • B-Lymphocytes / pathology
  • Biomarkers / metabolism
  • Bronchoalveolar Lavage Fluid / immunology
  • COVID-19 / immunology
  • COVID-19 / metabolism
  • COVID-19 / pathology*
  • Databases, Genetic
  • Humans
  • Hyaluronan Synthases / metabolism
  • Immunoglobulin A / metabolism
  • Interferon-alpha / metabolism
  • Lung / immunology
  • Lung / metabolism
  • Lung / pathology*
  • Matrix Metalloproteinases / metabolism
  • Mucin-1 / metabolism
  • Plasminogen Activator Inhibitor 1 / metabolism
  • RNA-Seq
  • SARS-CoV-2
  • Th17 Cells / metabolism
  • Th17 Cells / pathology

Substances

  • Biomarkers
  • IFNA1 protein, human
  • Immunoglobulin A
  • Interferon-alpha
  • MUC1 protein, human
  • Mucin-1
  • Plasminogen Activator Inhibitor 1
  • SERPINE1 protein, human
  • HAS2 protein, human
  • Hyaluronan Synthases
  • Matrix Metalloproteinases