Evidence map›Paper›PMID 36704839›Full record

ArticleAging cell2023

Treatment with the senolytics dasatinib/quercetin reduces SARS-CoV-2-related mortality in mice.

Andrés Pastor-Fernández, Antonio R Bertos, Arantzazu Sierra-Ramírez, Javier Del Moral-Salmoral, Javier Merino, Ana I de Ávila, Cristina Olagüe, Ricardo Villares, Gloria González-Aseguinolaza, María Ángeles Rodríguez and 6 more

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In one paragraph

Article in Aging cell, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Andrés Pastor-FernándezMetabolic Syndrome Group-BIOPROMET, Madrid Institute for Advanced Studies-IMDEA Food, CEI UAM+CSIC, Madrid, Spain.ORCID 0000-0002-8060-073X
Antonio R BertosDepartment of Internal Medicine and Surgical Animal, Faculty of Veterinary/VISAVET Centre, Complutense University of Madrid, Madrid, Spain.
Arantzazu Sierra-RamírezMetabolic Syndrome Group-BIOPROMET, Madrid Institute for Advanced Studies-IMDEA Food, CEI UAM+CSIC, Madrid, Spain.
Javier Del Moral-SalmoralDepartamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Javier MerinoDepartamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Ana I de ÁvilaCentro de Biología Molecular Severo Ochoa (CSIC-UAM), Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Cristina OlagüeDivision of Gene Therapy and Regulation of Gene Expression, CIMA Universidad de Navarra, Pamplona, Spain.
Ricardo VillaresCentro Nacional de Biotecnología (CNB-CSIC), Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.
Gloria González-AseguinolazaDivision of Gene Therapy and Regulation of Gene Expression, CIMA Universidad de Navarra, Pamplona, Spain.
María Ángeles RodríguezInstitute of Biomedicine of Seville (IBiS), Spanish National Research Council (CSIC), University of Seville, Virgen del Rocio University Hospital, Seville, Spain.
Manuel FresnoDepartamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Nuria GironésDepartamento de Biología Molecular, Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Matilde BustosInstitute of Biomedicine of Seville (IBiS), Spanish National Research Council (CSIC), University of Seville, Virgen del Rocio University Hospital, Seville, Spain.
Cristian SmerdouDivision of Gene Therapy and Regulation of Gene Expression, CIMA Universidad de Navarra, Pamplona, Spain.
Pablo Jose Fernandez-MarcosMetabolic Syndrome Group-BIOPROMET, Madrid Institute for Advanced Studies-IMDEA Food, CEI UAM+CSIC, Madrid, Spain.ORCID 0000-0003-3515-4125
Cayetano von KobbeCentro de Biología Molecular Severo Ochoa (CSIC-UAM), Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain.ORCID 0000-0003-3895-3790

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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-CoV-2 may be related to the post-COVID-19 sequelae described to date. These results place senescent cells as central targets for the treatment of COVID-19, and make D/Q a new and promising therapeutic tool.

Indexed as

COVID-19QuercetinAnimalsCellular SenescenceDasatinibHumansMicePandemicsSARS-CoV-2SenotherapeuticsDasatinibQuercetinSenotherapeuticscellular senescenceCOVID-19SARS-CoV-2senolyticssurvival

Identifiers

PMID36704839
PMCPMC10014049

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read61
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.