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      Effectiveness of an immunocastration vaccine formulation to reduce the gonadal function in female and male mice by Th1/Th2 immune response.

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          Abstract

          Immunocastration 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 ± 0.22 and 4.08 ± 0.39) and antral follicles (1.17 ± 0.32 and 4.5 ± 0.38) 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.

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          Author and article information

          Journal
          Theriogenology
          Theriogenology
          Elsevier BV
          1879-3231
          0093-691X
          Oct 01 2016
          : 86
          : 6
          Affiliations
          [1 ] Laboratory of Veterinary Vaccines, Department of Animal Biology, Faculty of Veterinary and Animal Science, University of Chile, Santiago, Chile.
          [2 ] Laboratory of Ecosystems' Health, Veterinary Medicine School, Faculty of Ecology and Natural Resources, Universidad Andrés Bello, Santiago, Chile.
          [3 ] California Animal Health and Food Safety Laboratory, University of California, San Bernardino, California, USA.
          [4 ] Department of Preventive Medicine, Faculty of Veterinary and Animal Science, University of Chile, Santiago, Chile.
          [5 ] Department of Animal Production, Faculty of Veterinary and Animal Science, University of Chile, Santiago, Chile.
          [6 ] Immunology Department, ICBP and Faculty of Medical Science Victoria de Girón, University of Medical Science of Havana, Cuba.
          [7 ] Laboratory of Veterinary Vaccines, Department of Animal Biology, Faculty of Veterinary and Animal Science, University of Chile, Santiago, Chile. Electronic address: leosaenz@uchile.cl.
          Article
          S0093-691X(16)30219-9
          10.1016/j.theriogenology.2016.05.019
          27344434
          d2f095e1-0ea6-4955-8fe0-662ee617046c
          History

          Immunocastration,Vaccine,Chitosan,GnRH
          Immunocastration, Vaccine, Chitosan, GnRH

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