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dc.creatorNavinés-Ferrer, A. (Arnau)-
dc.creatorSerrano-Candelas, E. (Eva)-
dc.creatorLafuente, A. (A.)-
dc.creatorMuñoz-Cano, R. (Rosa)-
dc.creatorMartín, M. (Margarita)-
dc.creatorGastaminza, G. (Gabriel)-
dc.date.accessioned2023-03-13T09:16:26Z-
dc.date.available2023-03-13T09:16:26Z-
dc.date.issued2018-
dc.identifier.citationNavinés-Ferrer, A. (Arnau); Serrano-Candelas, E. (Eva); Lafuente, A. (A.); et al. "MRGPRX2-mediated mast cell response to drugs used in perioperative procedures and anaesthesia". Scientific reports. 8 (1), 2018, 11628es
dc.identifier.issn2045-2322-
dc.identifier.urihttps://hdl.handle.net/10171/65666-
dc.description.abstractThe study of anaphylactoid reactions during perioperative procedures and anaesthesia represents a diagnostic challenge for allergists, as many drugs are administered simultaneously, and approximately half of them trigger allergic reactions without a verifiable IgE-mediated mechanism. Recently, mast cell receptor MRGPRX2 has been identified as a cause of pseudo-allergic drug reactions. In this study, we analyse the ability of certain drugs used during perioperative procedures and anaesthesia to induce MRGPRX2-dependent degranulation in human mast cells and sera from patients who experienced an anaphylactoid reaction during the perioperative procedure. Using a β-hexosaminidase release assay, several drugs were seen to cause mast cell degranulation in vitro in comparison with unstimulated cells, but only morphine, vancomycin and cisatracurium specifically triggered this receptor, as assessed by the release of β-hexosaminidase in the control versus the MRGPRX2-silenced cells. The same outcome was seen when measuring degranulation based on the percentage of CD63 expression at identical doses. Unlike that of the healthy controls, the sera of patients who had experienced an anaphylactoid reaction induced mast-cell degranulation. The degranulation ability of these sera decreased when MRGPRX2 was silenced. In conclusion, MRGPRX2 is a candidate for consideration in non-IgE-mediated allergic reactions to some perioperative drugs, reinforcing its role in mast cell responses and their pathophysiology.es_ES
dc.description.sponsorshipThis work was supported by the following grants: PI1200332, issued by the Fondo de Investigaciones Sanitarias; SAF2015-68124-R, issued by MINECO-FEDER (UE); and a grant issued by the Instituto de Salud Carlos III (ISCIII), co-founded by the Fondo Europeo de Desarrollo Regional (FEDER) for the Thematic Networks and Cooperative Research Centers: ARADyAL (RD16/0006/0031 and RD16/0006/0007). AN-F was supported by a grant from Fundación Gangoiti Barrera. RM-C is a recipient of a Juan Rodes Fellowship (ISCIII).es_ES
dc.language.isoenges_ES
dc.publisherNature Researches_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/Proyectos de I+D+I dentro del Programa Estatal Retos de la Sociedad (2015)/SAF2015-68124-R/ES/REGULACION DE LA EXPRESION Y FUNCION DE KIT Y PDGFRALFA POR LA MOLECULA ADAPTADORA 3BP2. IMPLICACION EN LA DIFERENCIACION Y MIGRACION MASTOCITARIA Y EN PATOLOGIAes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectAnaphylactoid reactionses_ES
dc.subjectPerioperative procedureses_ES
dc.subjectAnaesthesiaes_ES
dc.subjectMast cell receptores_ES
dc.titleMRGPRX2-mediated mast cell response to drugs used in perioperative procedures and anaesthesiaes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.description.noteThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.es_ES
dc.identifier.doi10.1038/s41598-018-29965-8-
dadun.citation.number1es_ES
dadun.citation.publicationNameScientific reportses_ES
dadun.citation.startingPage11628es_ES
dadun.citation.volume8es_ES

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