Evaluation of different heterologous prime-boost immunization strategies against Babesia bovis using viral vectored and protein-adjuvant vaccines based on a chimeric multi-antigen

Protection against the intraerythrocytic bovine parasite Babesia bovis requires both humoral and cellular immune responses. Therefore, tailored combinations of immunogens targeted at both arms of the immune system are strategies of choice to pursue sterilizing immunity. In this study, different hete...

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Main Authors: Jaramillo Ortiz, Jose Manuel, Molinari, Maria Paula, Gravisaco, Marí­a José, Paoletta, Martina, Montenegro, Valeria Noely, Wilkowsky, Silvina Elizabeth
Format: Artículo
Language:Inglés
Published: 2017
Subjects:
Online Access:http://hdl.handle.net/20.500.12123/1150
http://www.sciencedirect.com/science/article/pii/S0264410X16303796?via%3Dihub
https://link.springer.com/article/10.1007%2Fs00299-016-2026-7
https://doi.org/10.1016/j.vaccine.2016.05.053
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author Jaramillo Ortiz, Jose Manuel
Molinari, Maria Paula
Gravisaco, Marí­a José
Paoletta, Martina
Montenegro, Valeria Noely
Wilkowsky, Silvina Elizabeth
author_browse Gravisaco, Marí­a José
Jaramillo Ortiz, Jose Manuel
Molinari, Maria Paula
Montenegro, Valeria Noely
Paoletta, Martina
Wilkowsky, Silvina Elizabeth
author_facet Jaramillo Ortiz, Jose Manuel
Molinari, Maria Paula
Gravisaco, Marí­a José
Paoletta, Martina
Montenegro, Valeria Noely
Wilkowsky, Silvina Elizabeth
author_sort Jaramillo Ortiz, Jose Manuel
collection INTA Digital
description Protection against the intraerythrocytic bovine parasite Babesia bovis requires both humoral and cellular immune responses. Therefore, tailored combinations of immunogens targeted at both arms of the immune system are strategies of choice to pursue sterilizing immunity. In this study, different heterologous prime-boost vaccination schemes were evaluated in mice to compare the immunogenicity induced by a recombinant adenovirus, a modified vaccinia Ankara vector or a subunit vaccine all expressing a chimeric multi-antigen. This multi-antigen includes the immunodominant B and T cell epitopes of three B. bovis proteins: Merozoite Surface Antigen - 2c (MSA-2c), Rhoptry Associated Protein - 1 (RAP-1) and Heat Shock Protein 20 (HSP20). Both priming with the adenovirus or recombinant multi-antigen and boosting with the modified vaccinia Ankara vector achieved a high degree of activation of TNFα and IFNγ-secreting CD4(+) and CD8(+) specific T cells 60days after the first immunization. High titers of specific IgG antibodies were also detected at the same time point and lasted up to day 120 of the first immunization. Only the adenovirus - MVA combination triggered a marked isotype skew for the IgG2a antibody subclass meanwhile for the other immune traits analyzed here, both vaccination schemes showed similar performances. The immunological characterization in the murine model of these rationally designed immunogens led us to propose that adenoviruses as well as the bacterially expressed multi-antigen are highly reliable primer candidates to be considered in future experiments in cattle to test protection against bovine babesiosis
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spelling INTA11502019-03-22T13:38:30Z Evaluation of different heterologous prime-boost immunization strategies against Babesia bovis using viral vectored and protein-adjuvant vaccines based on a chimeric multi-antigen Jaramillo Ortiz, Jose Manuel Molinari, Maria Paula Gravisaco, Marí­a José Paoletta, Martina Montenegro, Valeria Noely Wilkowsky, Silvina Elizabeth Enfermedades de los Animales Babesia Bovis Vacuna Inmunización Animal Diseases Vaccines Immunization Protection against the intraerythrocytic bovine parasite Babesia bovis requires both humoral and cellular immune responses. Therefore, tailored combinations of immunogens targeted at both arms of the immune system are strategies of choice to pursue sterilizing immunity. In this study, different heterologous prime-boost vaccination schemes were evaluated in mice to compare the immunogenicity induced by a recombinant adenovirus, a modified vaccinia Ankara vector or a subunit vaccine all expressing a chimeric multi-antigen. This multi-antigen includes the immunodominant B and T cell epitopes of three B. bovis proteins: Merozoite Surface Antigen - 2c (MSA-2c), Rhoptry Associated Protein - 1 (RAP-1) and Heat Shock Protein 20 (HSP20). Both priming with the adenovirus or recombinant multi-antigen and boosting with the modified vaccinia Ankara vector achieved a high degree of activation of TNFα and IFNγ-secreting CD4(+) and CD8(+) specific T cells 60days after the first immunization. High titers of specific IgG antibodies were also detected at the same time point and lasted up to day 120 of the first immunization. Only the adenovirus - MVA combination triggered a marked isotype skew for the IgG2a antibody subclass meanwhile for the other immune traits analyzed here, both vaccination schemes showed similar performances. The immunological characterization in the murine model of these rationally designed immunogens led us to propose that adenoviruses as well as the bacterially expressed multi-antigen are highly reliable primer candidates to be considered in future experiments in cattle to test protection against bovine babesiosis Inst. de Biotecnología Fil: Jaramillo Ortiz, Jose Manuel. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina Fil: Molinari, Maria Paula. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina Fil: Gravisaco, Marí­a José. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina Fil: Paoletta, Martina. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina Fil: Montenegro, Valeria Noely. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina Fil: Wilkowsky, Silvina Elizabeth. Instituto Nacional de Tecnología Agropecuaria (INTA). Instituto de Biotecnología; Argentina 2017-09-06T14:29:09Z 2017-09-06T14:29:09Z 2016 info:ar-repo/semantics/artículo info:eu-repo/semantics/article info:eu-repo/semantics/acceptedVersion http://hdl.handle.net/20.500.12123/1150 http://www.sciencedirect.com/science/article/pii/S0264410X16303796?via%3Dihub https://link.springer.com/article/10.1007%2Fs00299-016-2026-7 0264-410X https://doi.org/10.1016/j.vaccine.2016.05.053 eng info:eu-repo/semantics/restrictedAccess application/pdf Vaccine 34 (33) : 3913-3919. (July 2016)
spellingShingle Enfermedades de los Animales
Babesia Bovis
Vacuna
Inmunización
Animal Diseases
Vaccines
Immunization
Jaramillo Ortiz, Jose Manuel
Molinari, Maria Paula
Gravisaco, Marí­a José
Paoletta, Martina
Montenegro, Valeria Noely
Wilkowsky, Silvina Elizabeth
Evaluation of different heterologous prime-boost immunization strategies against Babesia bovis using viral vectored and protein-adjuvant vaccines based on a chimeric multi-antigen
title Evaluation of different heterologous prime-boost immunization strategies against Babesia bovis using viral vectored and protein-adjuvant vaccines based on a chimeric multi-antigen
title_full Evaluation of different heterologous prime-boost immunization strategies against Babesia bovis using viral vectored and protein-adjuvant vaccines based on a chimeric multi-antigen
title_fullStr Evaluation of different heterologous prime-boost immunization strategies against Babesia bovis using viral vectored and protein-adjuvant vaccines based on a chimeric multi-antigen
title_full_unstemmed Evaluation of different heterologous prime-boost immunization strategies against Babesia bovis using viral vectored and protein-adjuvant vaccines based on a chimeric multi-antigen
title_short Evaluation of different heterologous prime-boost immunization strategies against Babesia bovis using viral vectored and protein-adjuvant vaccines based on a chimeric multi-antigen
title_sort evaluation of different heterologous prime boost immunization strategies against babesia bovis using viral vectored and protein adjuvant vaccines based on a chimeric multi antigen
topic Enfermedades de los Animales
Babesia Bovis
Vacuna
Inmunización
Animal Diseases
Vaccines
Immunization
url http://hdl.handle.net/20.500.12123/1150
http://www.sciencedirect.com/science/article/pii/S0264410X16303796?via%3Dihub
https://link.springer.com/article/10.1007%2Fs00299-016-2026-7
https://doi.org/10.1016/j.vaccine.2016.05.053
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