Publication:
Hyperinflammation and Fibrosis in Severe COVID-19 Patients: Galectin-3, a Target Molecule to Consider.

dc.contributor.authorGarcia-Revilla, Juan
dc.contributor.authorDeierborg, Tomas
dc.contributor.authorVenero, Jose Luis
dc.contributor.authorBoza-Serrano, Antonio
dc.date.accessioned2023-02-09T09:41:40Z
dc.date.available2023-02-09T09:41:40Z
dc.date.issued2020-08-18
dc.description.abstractCOVID-19 disease have become so far the most important sanitary crisis in the XXI century. In light of the events, any clinical resource should be considered to alleviate this crisis. Severe COVID-19 cases present a so-called cytokine storm as the most life-threatening symptom accompanied by lung fibrosis. Galectin-3 has been widely described as regulator of both processes. Hereby, we present compelling evidences on the potential role of galectin-3 in COVID-19 in the regulation of the inflammatory response, fibrosis and infection progression. Moreover, we provide a strong rationale of the utility of measuring plasma galectin-3 as a prognosis biomarker for COVID-19 patients and propose that inhibition of galectin-3 represents a feasible and promising new therapeutical approach.
dc.identifier.doi10.3389/fimmu.2020.02069
dc.identifier.essn1664-3224
dc.identifier.pmcPMC7461806
dc.identifier.pmid32973815
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461806/pdf
dc.identifier.unpaywallURLhttps://www.frontiersin.org/articles/10.3389/fimmu.2020.02069/pdf
dc.identifier.urihttp://hdl.handle.net/10668/16312
dc.journal.titleFrontiers in immunology
dc.journal.titleabbreviationFront Immunol
dc.language.isoen
dc.organizationInstituto de Biomedicina de Sevilla-IBIS
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number2069
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectCOVID-19
dc.subjectbiomarker
dc.subjectcytokine storm
dc.subjectfibrosis
dc.subjectgalectin-3
dc.subject.meshAngiotensin-Converting Enzyme 2
dc.subject.meshAnimals
dc.subject.meshBetacoronavirus
dc.subject.meshBiomarkers
dc.subject.meshBlood Proteins
dc.subject.meshCOVID-19
dc.subject.meshCoronavirus Infections
dc.subject.meshCytokines
dc.subject.meshDisease Progression
dc.subject.meshGalectin 3
dc.subject.meshGalectins
dc.subject.meshHost-Pathogen Interactions
dc.subject.meshHumans
dc.subject.meshInflammation
dc.subject.meshMolecular Targeted Therapy
dc.subject.meshPandemics
dc.subject.meshPeptidyl-Dipeptidase A
dc.subject.meshPneumonia, Viral
dc.subject.meshPrognosis
dc.subject.meshPulmonary Fibrosis
dc.subject.meshSARS-CoV-2
dc.subject.meshSeverity of Illness Index
dc.subject.meshSpike Glycoprotein, Coronavirus
dc.titleHyperinflammation and Fibrosis in Severe COVID-19 Patients: Galectin-3, a Target Molecule to Consider.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number11
dspace.entity.typePublication

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