Skip to main navigation Skip to search Skip to main content

Combating pan-coronavirus infection by indomethacin through simultaneously inhibiting viral replication and inflammatory response

  • College of Life Sciences, Northwest A&F University (Yangling)
  • Xuzhou Medical University
  • University of Tartu
  • Norwegian University of Science and Technology

Research output: Contribution to journalArticleAcademicpeer-review

30 Citations (Scopus)
73 Downloads (Pure)

Abstract

Severe infections with coronaviruses are often accompanied with hyperinflammation, requiring therapeutic strategies to simultaneously tackle the virus and inflammation. By screening a safe-in-human broad-spectrum antiviral agents library, we identified that indomethacin can inhibit pan-coronavirus infection in human cell and airway organoids models. Combining indomethacin with oral antiviral drugs authorized for treating COVID-19 results in synergistic anti-coronavirus activity. Coincidentally, screening a library of FDA-approved drugs identified indomethacin as the most potent potentiator of interferon response through increasing STAT1 phosphorylation. Combining indomethacin with interferon-alpha exerted synergistic antiviral effects against multiple coronaviruses. The anti-coronavirus activity of indomethacin is associated with activating interferon response. In a co-culture system of lung epithelial cells with macrophages, indomethacin inhibited both viral replication and inflammatory response. Collectively, indomethacin is a pan-coronavirus inhibitor that can simultaneously inhibit virus-triggered inflammatory response. The therapeutic potential of indomethacin can be further augmented by combining it with oral antiviral drugs or interferon-alpha.

Original languageEnglish
Article number107631
JournaliScience
Volume26
Issue number9
DOIs
Publication statusPublished - 15 Sept 2023

Bibliographical note

© 2023 The Author(s).

Fingerprint

Dive into the research topics of 'Combating pan-coronavirus infection by indomethacin through simultaneously inhibiting viral replication and inflammatory response'. Together they form a unique fingerprint.

Cite this