The suboptimal fibrinolytic response in COVID-19 is dictated by high PAI-1

J Thromb Haemost. 2022 Oct;20(10):2394-2406. doi: 10.1111/jth.15806. Epub 2022 Jul 21.

Abstract

Background: Severe COVID-19 disease is associated with thrombotic complications and extensive fibrin deposition. This study investigates whether the hemostatic complications in COVID-19 disease arise due to dysregulation of the fibrinolytic system.

Methods: This prospective study analyzed fibrinolytic profiles of 113 patients hospitalized with COVID-19 disease with 24 patients with non-COVID-19 respiratory infection and healthy controls. Antigens were quantified by Ella system or ELISA, clot lysis by turbidimetric assay, and plasminogen activator inhibitor-1 (PAI-1)/plasmin activity using chromogenic substrates. Clot structure was visualized by confocal microscopy.

Results: PAI-1 and its cofactor, vitronectin, are significantly elevated in patients with COVID-19 disease compared with those with non-COVID-19 respiratory infection and healthy control groups. Thrombin activatable fibrinolysis inhibitor and tissue plasminogen activator were elevated in patients with COVID-19 disease relative to healthy controls. PAI-1 and tissue plasminogen activator (tPA) were associated with more severe COVID-19 disease severity. Clots formed from COVID-19 plasma demonstrate an altered fibrin network, with attenuated fiber length and increased branching. Functional studies reveal that plasmin generation and clot lysis were markedly attenuated in COVID-19 disease, while PAI-1 activity was elevated. Clot lysis time significantly correlated with PAI-1 levels. Stratification of COVID-19 samples according to PAI-1 levels reveals significantly faster lysis when using the PAI-1 resistant (tPA) variant, tenecteplase, over alteplase lysis.

Conclusion: This study shows that the suboptimal fibrinolytic response in COVID-19 disease is directly attributable to elevated levels of PAI-1, which attenuate plasmin generation. These data highlight the important prognostic potential of PAI-1 and the possibility of using pre-existing drugs, such as tenecteplase, to treat COVID-19 disease and potentially other respiratory diseases.

Keywords: COVID-19; PAI-1; fibrin; fibrinolysis; vitronectin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • COVID-19 Drug Treatment*
  • Carboxypeptidase B2*
  • Chromogenic Compounds
  • Fibrin
  • Fibrinolysin / pharmacology
  • Fibrinolysis
  • Hemostatics* / pharmacology
  • Humans
  • Plasminogen Activator Inhibitor 1
  • Prospective Studies
  • Tenecteplase
  • Thrombosis* / drug therapy
  • Tissue Plasminogen Activator / pharmacology
  • Vitronectin

Substances

  • Chromogenic Compounds
  • Hemostatics
  • Plasminogen Activator Inhibitor 1
  • Vitronectin
  • Fibrin
  • Carboxypeptidase B2
  • Tissue Plasminogen Activator
  • Fibrinolysin
  • Tenecteplase