Please use this identifier to cite or link to this item: http://www.repositorio.ufop.br/handle/123456789/7274
Title: Immunogenicity in dogs of three recombinant antigens (TSA, LeiF and LmSTI1) potential vaccine for canine visceral leishmaniasis.
Authors: Fujiwara, Ricardo Toshio
Vale, André Macedo
Silva, João Carlos França da
Costa, Roberto Teodoro da
Quetz, Josiane da Silva
Martins Filho, Olindo Assis
Reis, Alexandre Barbosa
Oliveira, Rodrigo Corrêa de
Coelho, George Luiz Lins Machado
Bueno, Lilian Lacerda
Bethony, Jeffrey Michael
Frank, Glen
Nascimento, Evaldo do
Genaro, Odair
Mayrink, Wilson
Reed, Steven G.
Campos Neto, Antonio
Keywords: Leishmania chagasi
Vaccine
Issue Date: 2005
Citation: FUHIWARA, R. T. et al. Immunogenicity in dogs of three recombinant antigens (TSA, LeiF and LmSTI1) potential vaccine for canine visceral leishmaniasis. Veterinary Research, v. 36, p.827-838, 2005. Disponível em: <http://www.vetres.org/articles/vetres/abs/2005/05/v4085/v4085.html>. Acesso em: 10 out. 2016.
Abstract: Control of canine visceral leishmaniasis (VL) remains a difficult and serious problem mostly because there is no reliable and effective vaccine available to prevent this disease. A mixture of three recombinant leishmanial antigens (TSA, LeIF and LmSTI1) encoded by three genes highly conserved in the Leishmania genus have been shown to induce excellent protection against infection in both murine and simian models of cutaneous leishmaniasis. A human clinical trial with these antigens is currently underway. Because of the high degree of conservation, these antigens might be useful vaccine candidates for VL as well. In the present study, using the dog model of the visceral disease, we evaluated the immunogenicity of these three antigens formulated with two different adjuvants, MPL-SE® and AdjuPrime®. The results were compared with a whole parasite vaccine formulated with BCG as the adjuvant. In order to investigate if sensitization with the recombinant antigens would result in recognition of the corresponding native parasite antigens upon infection, the animals were exposed for four weeks after the termination of the immunization protocol with the recombinant antigens to a low number of L. chagasi promastigotes, an etiological agent of VL. Immune response was evaluated by quantitative ELISA in the animal sera before and after exposure to the viable parasites. Both antigen specific IgG1 and IgG2 antibody levels were measured. Immunization of dogs with the recombinant antigens formulated in either MPL-SE® or AdjuPrime® resulted in high antibody levels particularly to LmSTI1. In addition, this immunization although to low levels, resulted in the development of antibody response to the whole parasite lysate. Importantly, experimental exposure with low numbers of culture forms of L. chagasi promastigotes caused a clear boost in the immune response to both the recombinant antigens and the corresponding native molecules. The boost response was predominantly of the IgG2 isotype in animals primed with the recombinant antigens plus MPL-SE®. In contrast, animals primed with the recombinant antigens formulated in AdjuPrime® as well as animals vaccinated with crude antigen preparation responded with mixed IgG1/IgG2 isotypes. These results point to the possible use of this antigen cocktail formulated with the adjuvant MPL-SE® in efficacy field trials against canine VL.
URI: http://www.repositorio.ufop.br/handle/123456789/7274
metadata.dc.identifier.uri2: http://www.vetres.org/articles/vetres/abs/2005/05/v4085/v4085.html
ISSN: 12979716
Appears in Collections:DEFAR - Artigos publicados em periódicos

Files in This Item:
File Description SizeFormat 
ARTIGO_ImmunogenicityDogsThree.pdf345,83 kBAdobe PDFView/Open    Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.