Publication:
Histamine and mast cell activator compound 48/80 are safe but inefficient systemic adjuvants for gilthead seabream vaccination

dc.contributor.authorGómez González N.E., Cabas I.
dc.contributor.authorMontero J., García Alcázar A
dc.contributor.authorMulero Méndez, Victoriano Francisco
dc.contributor.authorGarcía Ayala, Alfonsa
dc.contributor.departmentBiología Celular e Histología
dc.date.accessioned2021-02-13T19:20:56Z
dc.date.available2021-02-13T19:20:56Z
dc.date.issued2017-02-10
dc.description.abstractHistamine has a key role in the regulation of inflammatory and innate immune responses in vertebrates. Gilthead seabream (Sparus aurata L.), a marine hermaphrodite teleost of great commercial value, was the first fish species shown to possess histamine-containing mast cells (MCs) at mucosal tissues. MCs are highly abundant in the peritoneal exudate of gilthead seabream and compound 48/80 (Co 48/80), often used to promote MC activation and histamine release, is able to promote histamine release from gilthead seabream MCs in vitro and in vivo. The aim of the present study was to analyze the effect of histamine and Co 48/80 on the immune responses of gilthead seabream. For this purpose, histamine and Co 48/80 were intraperitoneally injected alone or combined with 109 heat-killed Vibrio anguillarum cells and their effects on head kidney and peritoneal exudate were analyzed. The results indicated that although histamine and Co 48/80 were both able to alter the percentage of peritoneal exudate and head kidney immune cell types, only Co 48/80 increased reactive oxygen species production by peritoneal leukocytes. In addition, histamine, but not Co 48/80, was able to slightly impair the humoral adaptive immune response, i.e. production of specific IgM to V. anguillarum. Notably, both histamine and Co 48/80 reduced the expression of the gene encoding histamine receptor H2 in peritoneal exudate leukocytes. These results show for the first time in fish that although systemic administration of histamine and Co 48/80 is safe, neither compound can be regarded as an efficient adjuvant for gilthead seabream vaccination.es
dc.formatapplication/pdfes
dc.format.extent20es
dc.identifier.citationDevelopmental and Comparative Immunology 72: 1-8, 2017
dc.identifier.doihttp:// dx.doi.org/10.1016/j.dd.2017.06.002
dc.identifier.issn0145-305X
dc.identifier.urihttp://hdl.handle.net/10201/103201
dc.languageenges
dc.publisherElsevieres
dc.relationÁmbito del proyecto (Europeo, nacional o regional): Nacional; regional Agencia/entidad financiadora: Ministerio de Economía y Competitividad; Fundación Séneca (Comunidad Autónoma de la Región de Murcia) Convocatoria: Programa Estatal de Investigación, Desarrollo e Innovación Orientada a los Retos de la Sociedad, Convocatoria 2014, Modalidad 1: «Proyectos de I+D+I; Programa de ayudas a las Unidades y Grupos de Excelencia Científica de la Región de Murcia Nombre del proyecto: Análisis de las vías de actuación de contaminantes de origen farmacéutico en la respuesta inmunitaria celular y en la espermatogénesis en peces; Improvement of the Mediterranean aquaculture production by biotechnological tools Código: AGL2014-53167-C3-1-R; 19883 /GERM/15es
dc.relation.isreplacedbyhttps://www.sciencedirect.com/science/article/pii/S0145305X16305079es
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectHistamine, Compound 48/80, Gilthead seabream, Vaccinationes
dc.subject.otherCDU::5 - Ciencias puras y naturaleses
dc.titleHistamine and mast cell activator compound 48/80 are safe but inefficient systemic adjuvants for gilthead seabream vaccinationes
dc.typeinfo:eu-repo/semantics/articlees
dspace.entity.typePublicationes
relation.isAuthorOfPublication369f9ade-8896-4d91-84c5-e3f94a526070
relation.isAuthorOfPublicationbe292a3e-c75a-428f-ab50-f5dff0b81234
relation.isAuthorOfPublication.latestForDiscovery369f9ade-8896-4d91-84c5-e3f94a526070
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