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dc.contributor.author | BOTELLA ASUNCION, PABLO | es_ES |
dc.contributor.author | Rivero-Buceta, Eva María | es_ES |
dc.contributor.author | VIDAURRE AGUT, CARLA | es_ES |
dc.contributor.author | Lama, Raquel | es_ES |
dc.contributor.author | Rey-Campos, Magalí | es_ES |
dc.contributor.author | Moreno, Alejandro | es_ES |
dc.contributor.author | Mendoza, Laura | es_ES |
dc.contributor.author | Mingo-Casas, Patricia | es_ES |
dc.contributor.author | Escribano-Romero, Estela | es_ES |
dc.contributor.author | Gutiérrez-Adán, Alfonso | es_ES |
dc.contributor.author | Saiz, Juan Carlos | es_ES |
dc.contributor.author | Smerdou, Cristian | es_ES |
dc.contributor.author | Gonzalez, Gloria | es_ES |
dc.contributor.author | Prósper, Felipe | es_ES |
dc.contributor.author | Argemí, Josepmaría | es_ES |
dc.contributor.author | San Miguel, Jesus | es_ES |
dc.contributor.author | Sánchez Cordón, Pedro J. | es_ES |
dc.contributor.author | Figueras, Antonio | es_ES |
dc.contributor.author | Quesada-Gómez, Jose Manuel | es_ES |
dc.contributor.author | Novoa, Beatriz | es_ES |
dc.contributor.author | Montoya, María | es_ES |
dc.contributor.author | Martín-Acebes, Miguel A. | es_ES |
dc.contributor.author | Pineda-Lucena, Antonio | es_ES |
dc.contributor.author | Benlloch Babiera, José María | es_ES |
dc.date.accessioned | 2024-07-24T18:03:04Z | |
dc.date.available | 2024-07-24T18:03:04Z | |
dc.date.issued | 2023-11 | es_ES |
dc.identifier.issn | 0753-3322 | es_ES |
dc.identifier.uri | http://hdl.handle.net/10251/206595 | |
dc.description.abstract | [EN] An archetypal anti-inflammatory compound against cytokine storm would inhibit it without suppressing the innate immune response. AG5, an anti-inflammatory compound, has been developed as synthetic derivative of andrographolide, which is highly absorbable and presents low toxicity. We found that the mechanism of action of AG5 is through the inhibition of caspase-1. Interestingly, we show with in vitro generated human monocyte derived dendritic cells that AG5 preserves innate immune response. AG5 minimizes inflammatory response in a mouse model of lipopolysaccharide (LPS)-induced lung injury and exhibits in vivo anti-inflammatory efficacy in the SARS-CoV-2-infected mouse model. AG5 opens up a new class of anti-inflammatories, since contrary to NSAIDs, AG5 is able to inhibit the cytokine storm, like dexamethasone, but, unlike corticosteroids, preserves adequately the innate immunity. This is critical at the early stages of any naïve infection, but particularly in SARS-CoV-2 infections. Furthermore, AG5 showed interesting antiviral activity against SARS-CoV-2 in humanized mice. | es_ES |
dc.description.sponsorship | This work has been supported by NextGenerationEU Recovery and Resilience Facility (RRF) through the PTI+ Global Health Platform of Spanish National Research Council, grants SGL2103023 (PBA), SGL2103053 (MMA) and SGL2103015 (MM); by Spanish National Research Council through the program Ayudas extraodinarias a proyectos de investigacion en el marco de las medidas urgentes extraodinarias para hacer frente al impacto economico ¿ y social del COVID19 , grants CSIC-COV19-093 (PBA) and CSIC-COV19-117 (MM); by Generalitat Valenciana through the program Ayudas urgentes para proyectos de investigacion, ¿ desarrollo tecnologico ¿ e innovacion ¿ (I+D+i) por la COVID-19 , grant GVA-COVID19/2021/059 (PBA); by the Conference of Rectors of the Spanish Universities, Spanish National Research Council and Banco Santander through the FONDO SUPERA COVID-19, grant CAPriCORn (JSM, JMB); by Severo Ochoa center of excellence program (grant CEX2021-001230-S) (PBA). | es_ES |
dc.language | Inglés | es_ES |
dc.publisher | Elsevier | es_ES |
dc.relation.ispartof | Biomedicine & Pharmacotherapy | es_ES |
dc.rights | Reconocimiento - No comercial - Sin obra derivada (by-nc-nd) | es_ES |
dc.subject | Cytokine storm | es_ES |
dc.subject | COVID-19 | es_ES |
dc.subject | Andrographolide | es_ES |
dc.subject | Dexamethasone | es_ES |
dc.subject | Innate immunity | es_ES |
dc.title | AG5 is a potent non-steroidal anti-inflammatory and immune regulator that preserves innate immunity | es_ES |
dc.type | Artículo | es_ES |
dc.identifier.doi | 10.1016/j.biopha.2023.115882 | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/Banco Santander//CAPriCORn/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/CSIC//SGL2103053/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/CSIC//SGL2103023/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/CSIC//SGL2103015/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/CSIC//CSIC-COV19-093/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/CSIC// CSIC-COV19-117/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/GVA// GVA-COVID19%2F2021%2F059/ | es_ES |
dc.relation.projectID | info:eu-repo/grantAgreement/MICINN//CEX2021-001230-S/ | es_ES |
dc.rights.accessRights | Abierto | es_ES |
dc.description.bibliographicCitation | Botella Asuncion, P.; Rivero-Buceta, EM.; Vidaurre Agut, C.; Lama, R.; Rey-Campos, M.; Moreno, A.; Mendoza, L.... (2023). AG5 is a potent non-steroidal anti-inflammatory and immune regulator that preserves innate immunity. Biomedicine & Pharmacotherapy. 169. https://doi.org/10.1016/j.biopha.2023.115882 | es_ES |
dc.description.accrualMethod | S | es_ES |
dc.relation.publisherversion | https://doi.org/10.1016/j.biopha.2023.115882 | es_ES |
dc.description.upvformatpinicio | 115882 | es_ES |
dc.type.version | info:eu-repo/semantics/publishedVersion | es_ES |
dc.description.volume | 169 | es_ES |
dc.relation.pasarela | S\510219 | es_ES |
dc.contributor.funder | Banco Santander | es_ES |
dc.contributor.funder | Generalitat Valenciana | es_ES |
dc.contributor.funder | Ministerio de Ciencia e Innovación | es_ES |
dc.contributor.funder | Consejo Superior de Investigaciones Científicas | es_ES |