Diacerein reduces inflammasome activation and SARS-CoV-2 virus replication: a proof-of-concept translational study
Helison R P Carmo, Alejandro Rossel Castillo, Isabella Bonilha, Erica I L Gomes, Joaquim Barreto, Filipe A Moura, Gustavo Gastão Davanzo, Lauar De Brito Monteiro, Stéfanie Primon Muraro, Gabriela Fabiano De Souza, Joseane Morari, Flávia Elisa Galdino, Natália S Brunetti, Guilherme Reis-De-Oliveira, Victor Corasolla Carregari, Wilson Nadruz, Daniel Martins-De-Souza, Alessandro S Farias, Licio A Velloso, José Luiz Proenca-Modena, Marcelo A Mori, Watson Loh, Deepak L Bhatt, Derek M Yellon, Sean M Davidson, Pedro G De Oliveira, Pedro M Moraes-Vieira, Andrei C Sposito
Frontiers in Pharmacology, doi:10.3389/fphar.2024.1402032
Background: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is linked to high mortality, primarily through an intense inflammatory response. Diacerein has emerged as a potential therapy for COVID-19 due to its potential impact in decreasing the inflammasome activation and coronavirus replication. This study aims to explore diacerein's influence in inhibiting both viral replication and the inflammatory response after SARS-CoV-2 infection.
Conflict of interest Amgen, AstraZeneca, Bayer, Beren, Boehringer Ingelheim, Boston Scientific, Bristol-Myers Squibb, Cardax, CellProthera, Cereno Scientific, Chiesi, CinCor, Cleerly, CSL Behring, Eisai, Ethicon, Faraday Pharmaceuticals, Ferring Pharmaceuticals, Forest Laboratories, Fractyl, Garmin, HLS Therapeutics, Idorsia, Ironwood, Ischemix, Janssen, Javelin, Lexicon, Lilly, Medtronic, Merck, Moderna, MyoKardia, NirvaMed, Novartis, Novo (FAPESP) . Dr. Pedro Gonç alves de Oliveira is responsible for R&D activities at TRB Pharma Indú stria Quí mica e Farmace utica Ltda, SP, Brazil. TRB Pharma is the owner of the product ARTRODAR ® a diacerein-based product for osteoarthritis treatment. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher's note All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2024.1402032/ full#supplementary-material
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"abstract": "<jats:sec><jats:title>Background</jats:title><jats:p>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is linked to high mortality, primarily through an intense inflammatory response. Diacerein has emerged as a potential therapy for COVID-19 due to its potential impact in decreasing the inflammasome activation and coronavirus replication. This study aims to explore diacerein’s influence in inhibiting both viral replication and the inflammatory response after SARS-CoV-2 infection.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Human peripheral blood mononuclear cells (PBMCs) were obtained from healthy volunteers and infected <jats:italic>in vitro</jats:italic> with SARS-CoV-2. Additionally, we carried out a pilot randomized, double-blind, placebo-controlled study with 14 participants allocated to diacerein (n = 7) or placebo (n = 7) therapies every 12 h for 10 days. The primary endpoint was change in plasma markers of inflammasome activation (NLRP3, caspase-1, and gasdermin-D).</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p><jats:italic>In vitro</jats:italic> protocols have shown that rhein, diacerein’s primary metabolite, decreased IL-1β secretion caused by SARS-CoV-2 infection in human PBMCs (<jats:italic>p</jats:italic> &lt; 0.05), and suppressed viral replication when administered either before or after the virus incubation (<jats:italic>p</jats:italic> &lt; 0.05). This later effect was, at least partially, attributed to its inhibitory effect on 3-chymotrypsin-like protease (SARS-CoV-2 3CL<jats:sup>pro</jats:sup>) and papain-like protease in the SARS-CoV-2 (SARS-CoV-2 PL<jats:sup>pro</jats:sup>) virus and in the phosphorylation of proteins related cytoskeleton network (<jats:italic>p</jats:italic> &lt; 0.05). Diacerein-treated COVID-19 patients presented a smaller area under the curve for NLRP3, caspase-1 and GSDM-D measured on days 2, 5, and 10 after hospitalization compared to those receiving a placebo (<jats:italic>p</jats:italic> &lt; 0.05).</jats:p></jats:sec><jats:sec><jats:title>Conclusion</jats:title><jats:p>The indicated mechanisms of action of diacerein/rhein can reduce viral replication and mitigate the inflammatory response related to SARS-CoV-2. These findings are preliminary and require confirmation in clinical trials.</jats:p></jats:sec>",
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