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dc.contributor.authorLeal, Yeny
dc.contributor.authorVelazquez, Janet
dc.contributor.authorHernandez, Liz
dc.contributor.authorSwain, Jaya Kumari
dc.contributor.authorRodríguez, Alianet Rodríguez
dc.contributor.authorMartínez, Rebeca
dc.contributor.authorGarcía, Claudia
dc.contributor.authorRamos, Yassel
dc.contributor.authorEstrada, Mario Pablo
dc.contributor.authorCarpio, Yamila
dc.date.accessioned2020-01-30T13:54:25Z
dc.date.available2020-01-30T13:54:25Z
dc.date.issued2019-06-11
dc.description.abstractThe development of vaccines employing conserved protein antigens, for instance ribosomal protein P0, has as disadvantage the high degree of identity between pathogen and host proteins due to possible induction of tolerance or auto antibodies in the host organism. To overcome this drawback, peptide-based vaccines have been designed with a proved high efficacy. The use of defined peptides as antigens has the problem that they are generally poor immunogenic unless coupled to a carrier protein. Several studies have established the potential for promiscuous T cell epitopes incorporated into chimeric peptides to enhance the immunogenicity in mammals. On the contrary, studies about the role of these epitopes on teleost immune system are scarce. Therefore, the main objective of our present study was to evaluate the potential of promiscuous T cell epitopes to boost specific IgM immune response in teleost fish against a peptide antigen. With this aim, we used a peptide of 35 amino acids from the ribosomal P0 protein of <i>Lepeophtheirus salmonis</i>, an important parasite in salmon aquaculture. We fused this peptide to the C-terminal of T cell epitopes from tetanus toxin and measles virus and produced the chimeric protein in <i>Escherichia coli</i>. Following vaccination, IgM antibody production was monitored in different immunization schemes in Tilapia, African catfish and Atlantic salmon. The results demonstrated for first time that the addition of T cell epitopes at the N-terminal of a target peptide increased IgM specific response in different teleost species, revealing the potential of this approach to develop peptide-based vaccines for aquaculture. The results are also of great importance in the context of vaccine development against sea lice using ribosomal protein P0 as antigen taking into account the key role of P0 in protein synthesis and other essential physiological processes.en_US
dc.identifier.citationLeal, Velazquez, Hernandez, Swain K, Rodríguez, Martínez, García, Ramos, Estrada, Carpio. Promiscuous T cell epitopes boosts specific IgM immune response against a P0 peptide antigen from sea lice in different teleost species. Fish and Shellfish Immunology. 2019;92:322-330en_US
dc.identifier.cristinIDFRIDAID 1712057
dc.identifier.doi10.1016/j.fsi.2019.06.018
dc.identifier.issn1050-4648
dc.identifier.issn1095-9947
dc.identifier.urihttps://hdl.handle.net/10037/17281
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.relation.journalFish and Shellfish Immunology
dc.relation.projectIDFiskeri- og havbruksnæringens forskningsfinansiering: 901461en_US
dc.relation.projectIDNofima AS: 12211en_US
dc.rights.accessRightsopenAccessen_US
dc.rights.holder© 2019 Elsevier Ltd. All rights reserved.en_US
dc.subjectVDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710en_US
dc.subjectVDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710en_US
dc.titlePromiscuous T cell epitopes boosts specific IgM immune response against a P0 peptide antigen from sea lice in different teleost speciesen_US
dc.type.versionsubmittedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US


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