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Authordc.contributor.authorSiel Siel, Daniela 
Authordc.contributor.authorVidal Vilches, Sonia 
Authordc.contributor.authorSevilla Reyes, Rafael 
Authordc.contributor.authorParedes, Rodolfo 
Authordc.contributor.authorCarvallo, Francisco 
Authordc.contributor.authorLapierre Acevedo, Lisette 
Authordc.contributor.authorMaino Menéndez, Mario 
Authordc.contributor.authorPérez, Oliver 
Authordc.contributor.authorSáenz Iturriaga, Leonardo Enrique 
Admission datedc.date.accessioned2016-12-28T14:32:58Z
Available datedc.date.available2016-12-28T14:32:58Z
Publication datedc.date.issued2016
Cita de ítemdc.identifier.citationTheriogenology 86 (2016) 1589–1598es_ES
Identifierdc.identifier.other10.1016/j.theriogenology.2016.05.019
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/142161
Abstractdc.description.abstractImmunocastration has emerged as an alternative to surgical castration in different animal species. This study examined the effectiveness of a new vaccine formulation for immunocastration using the biopolymer chitosan as adjuvant. First, female and male mice (n = 4), in three subsequent experiments were vaccinated at Days 1 and 30 of the study, to determine the immune response profile and gonadal alterations due to immunization. The results demonstrated that the vaccine was able to elicit strong antibody responses against native GnRH hormone (P < 0.01), with a T helper (Th) 1/Th2 immune response profile. Along with this, a suppression of gonadal activity with a decrease of luteal bodies (1.08 +/- 022 and 4.08 +/- 0.39) and antral follicles (1.17 +/- 0.32 and 4.5 +/- 038) in the ovaries of immunized females and control, respectively, and a reduction of seminiferous tubules size (142.3 +/-5.58 mm and 198.0 +/- 6.11 mm) and germinal cellular layers (3.58 +/- 0.26 and 5.08 +/- 0.29) of immunized males and control animals, respectively, were observed (P < 0.01). Then, in a study of long-term immune response due to vaccination in female and male mice (n = 4) from two subsequent experiments, a suppression of gonadal function and an induction of a Th1/Th2 immune response was also observed, determined by both, immunoglobulin and cytokine profiles, which lasted until the end of the study (7 months; P < 0.01). The findings of this study have demonstrated that vaccination with a new immunocastration vaccine inducing a Th1/Th2 immune response against GnRH (P < 0.01) elicit a decrease of gonadal function in male and female mice (P < 0.01). Owing to long-term duration of the antibody levels generated, this vaccine formulation appears as a promising alternative for immunocastration of several animal species where long-lasting reproductive block is needed. (C) 2016 Elsevier Inc. All rights reservedes_ES
Patrocinadordc.description.sponsorshipInitiation Into Research Competition Program - National Research Funding Competition (FONDECYT) 11080015es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherElsevieres_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceTheriogenologyes_ES
Keywordsdc.subjectImmunocastrationes_ES
Keywordsdc.subjectGnRHes_ES
Keywordsdc.subjectVaccinees_ES
Keywordsdc.subjectChitosanes_ES
Títulodc.titleEffectiveness of an immunocastration vaccine formulation to reduce the gonadal function in female and male mice by Th1/Th2 immune responsees_ES
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile