Targeting peptidyl-arginine deiminase 4 suppresses SARS-CoV-2 replication and modulates the inflammatory response

SARS-CoV-2, the causative agent of COVID-19, remains a global concern due to gaps in understanding its pathogenesis. Peptidyl-arginine deiminases (PADs) are emerging as key regulators of viral replication and inflammation. PADs catalyze the conversion of arginine into citrulline, a modification linked to autoimmune diseases. Here, we show that PAD-mediated citrullination plays a crucial role in SARS-CoV-2 infection. Using human cell lines and in K18-hACE2 transgenic mice infected with different SARS-CoV-2 strains, we demonstrate that viral replication is associated with increased PAD4 expression. Mass spectrometry shows 170 distinct differentially citrullinated proteins in infected cells and tissues. Importantly, PAD4 inhibition significantly reduces viral replication and restores a citrullination profile comparable to that of uninfected mice. These findings suggest that SARS-CoV-2 exploits PAD-mediated citrullination to enhance replication and inflammation. Thus, targeting PAD4 may represent a viable strategy to curb viral spread and mitigate COVID-19-associated hyperinflammation.

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Publication Details

Journal
iScience
Published
2026-02-17
DOI
https://doi.org/10.1016/j.isci.2026.115038
Primary Topic
Peptidase Inhibition and Analysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Targeting peptidyl-arginine deiminase 4 suppresses SARS-CoV-2 replication and modulates the inflammatory response

Marco De Andrea, Serena Delbue, Valeria Caneparo, Selina Pasquero et al.
iScience
Peptidase Inhibition and Analysis
article

Targeting peptidyl-arginine deiminase 4 suppresses SARS-CoV-2 replication and modulates the inflammatory response

Marco De Andrea, Serena Delbue, Valeria Caneparo, Selina Pasquero, Francesco Favero, Lucia Signorini, Robert M. Green, Beatrice Genova, Ranieri Verin, Anna Dalla Pietà, Ilaria Frasson, Alessandro Penna, Anna Tosi, Francesca Gugliesi, Webb Camille, Salvatore Villani, Antonio Rosato, Erika Del Grosso, Sara N. Richter, Sofia Tomasoni, Paul R. Thompson
article en

Abstract

SARS-CoV-2, the causative agent of COVID-19, remains a global concern due to gaps in understanding its pathogenesis. Peptidyl-arginine deiminases (PADs) are emerging as key regulators of viral replication and inflammation. PADs catalyze the conversion of arginine into citrulline, a modification linked to autoimmune diseases. Here, we show that PAD-mediated citrullination plays a crucial role in SARS-CoV-2 infection. Using human cell lines and in K18-hACE2 transgenic mice infected with different SARS-CoV-2 strains, we demonstrate that viral replication is associated with increased PAD4 expression. Mass spectrometry shows 170 distinct differentially citrullinated proteins in infected cells and tissues. Importantly, PAD4 inhibition significantly reduces viral replication and restores a citrullination profile comparable to that of uninfected mice. These findings suggest that SARS-CoV-2 exploits PAD-mediated citrullination to enhance replication and inflammation. Thus, targeting PAD4 may represent a viable strategy to curb viral spread and mitigate COVID-19-associated hyperinflammation.

iScienceVol. 29(3)
Università degli Studi del Piemonte Orientale “Amedeo Avogadro” (IT), University of Padua (IT), University of Massachusetts Chan Medical School (US), University of Milan (IT), Istituto Oncologico Veneto (IT), Department of Medical Sciences (BY), Department of Public Health (US), Piedmont University (US)
European Commission, Ministero dell’Istruzione, dell’Università e della Ricerca, Fondazione Umberto Veronesi, Università degli Studi di Torino, National Institutes of Health, Rijksinstituut voor Volksgezondheid en Milieu
Zero hunger
Openalex Percentile: Top 51%
Peptidase Inhibition and Analysis
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