<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pastor-Fernandez A</submitter><funding>China Shipbuilding Industry</funding><funding>Instituto de Salud Carlos III</funding><funding>Ministerio de Ciencia e Innovación</funding><pagination>e13771</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10014049</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(3)</volume><pubmed_abstract>The enormous societal impact of the ongoing COVID-19 pandemic has been particularly harsh for some social groups, such as the elderly. Recently, it has been suggested that senescent cells could play a central role in pathogenesis by exacerbating the pro-inflammatory immune response against SARS-CoV-2. Therefore, the selective clearance of senescent cells by senolytic drugs may be useful as a therapy to ameliorate the symptoms of COVID-19 in some cases. Using the established COVID-19 murine model K18-hACE2, we demonstrated that a combination of the senolytics dasatinib and quercetin (D/Q) significantly reduced SARS-CoV-2-related mortality, delayed its onset, and reduced the number of other clinical symptoms. The increase in senescent markers that we detected in the lungs in response to SARS</pubmed_abstract><journal>Aging cell</journal><pubmed_title>Treatment with the senolytics dasatinib/quercetin reduces SARS-CoV-2-related mortality in mice.</pubmed_title><pmcid>PMC10014049</pmcid><funding_grant_id>PID2020‐113888RB‐I00</funding_grant_id><funding_grant_id>SAF2017‐85766‐R</funding_grant_id><funding_grant_id>CSIC‐COV19‐014</funding_grant_id><funding_grant_id>COV20‐00755</funding_grant_id><funding_grant_id>PID2020‐114077RB‐I00</funding_grant_id><funding_grant_id>COV20‐00792</funding_grant_id><funding_grant_id>RYC‐2017‐22335</funding_grant_id><pubmed_authors>Del Moral-Salmoral J</pubmed_authors><pubmed_authors>Gonzalez-Aseguinolaza G</pubmed_authors><pubmed_authors>Smerdou C</pubmed_authors><pubmed_authors>Merino J</pubmed_authors><pubmed_authors>de Avila AI</pubmed_authors><pubmed_authors>Bertos AR</pubmed_authors><pubmed_authors>Girones N</pubmed_authors><pubmed_authors>Olague C</pubmed_authors><pubmed_authors>Fresno M</pubmed_authors><pubmed_authors>Sierra-Ramirez A</pubmed_authors><pubmed_authors>Fernandez-Marcos PJ</pubmed_authors><pubmed_authors>Rodriguez MA</pubmed_authors><pubmed_authors>Pastor-Fernandez A</pubmed_authors><pubmed_authors>von Kobbe C</pubmed_authors><pubmed_authors>Villares R</pubmed_authors><pubmed_authors>Bustos M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Treatment with the senolytics dasatinib/quercetin reduces SARS-CoV-2-related mortality in mice.</name><description>The enormous societal impact of the ongoing COVID-19 pandemic has been particularly harsh for some social groups, such as the elderly. Recently, it has been suggested that senescent cells could play a central role in pathogenesis by exacerbating the pro-inflammatory immune response against SARS-CoV-2. Therefore, the selective clearance of senescent cells by senolytic drugs may be useful as a therapy to ameliorate the symptoms of COVID-19 in some cases. Using the established COVID-19 murine model K18-hACE2, we demonstrated that a combination of the senolytics dasatinib and quercetin (D/Q) significantly reduced SARS-CoV-2-related mortality, delayed its onset, and reduced the number of other clinical symptoms. The increase in senescent markers that we detected in the lungs in response to SARS</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-06-28T03:04:51.025Z</modification><creation>2025-04-07T12:35:48.205Z</creation></dates><accession>S-EPMC10014049</accession><cross_references><pubmed>36704839</pubmed><doi>10.1111/acel.13771</doi></cross_references></HashMap>