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dc.contributor.authorSantos, Fernanda Nunes-
dc.contributor.authorBorja Cabrera, Gulnara Patricia-
dc.contributor.authorMyashiro, L. M.-
dc.contributor.authorGrechi, Juliana-
dc.contributor.authorReis, Alexandre Barbosa-
dc.contributor.authorMoreira, Márcio Antônio Batistela-
dc.contributor.authorMartins Filho, Olindo Assis-
dc.contributor.authorLuvizotto, Maria Cecília Rui-
dc.contributor.authorMenz, Ingrid-
dc.contributor.authorPessôa, L. M.-
dc.contributor.authorGonçalves, Pablo Rodrigues-
dc.contributor.authorPalatnik, Marcos-
dc.contributor.authorSouza, Clarisa Beatriz Palatnik de-
dc.date.accessioned2012-07-10T14:46:11Z-
dc.date.available2012-07-10T14:46:11Z-
dc.date.issued2007-
dc.identifier.citationSANTOS, F. N. et al. Immunotherapy against experimental canine visceral leishmaniasis with the saponin enriched-Leishmune ® vaccine. Vaccine, v. 25, n. 33, p. 6176-6190, ago. 2007. Disponível em: <https://www.sciencedirect.com/science/article/pii/S0264410X07006810>. Acesso em: 10 jul. 2012.pt_BR
dc.identifier.issn0264410X-
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/1042-
dc.description.abstractIn order to assess the immunotherapeutic potential on canine visceral leishmaniasis of the Leishmune ® vaccine, formulated with an increased adjuvant concentration (1 mg of saponin rather than 0.5 mg), 24 mongrel dogs were infected with Leishmania (L.) chagasi . The enriched-Leishmune ® vaccine was injected on month 6, 7 and 8 after infection, when animals were seropositive and symptomatic. The control group were injected with a saline solution. Leishmune ® -treated dogs showed significantly higher levels of anti-FML IgG antibodies (ANOVA; p < 0.0001), a higher and stable IgG2 and a decreasing IgG1 response, pointing to a TH1 T cell mediated response. The vaccine had the following effects: it led to more positive delayed type hypersensitivity reactions against Leishmania lysate in vaccinated dogs (75%) than in controls (50%), to a decreased average of CD4+ Leishmania -specific lymphocytes in saline controls (32.13%) that fell outside the 95% confidence interval of the vaccinees (41.62%, CI95% 43.93–49.80) and an increased average of the clinical scores from the saline controls (17.83) that falls outside the 95% confidence interval for the Leishmune ® immunotherapy-treated dogs (15.75, CI95% 13.97–17.53). All dogs that received the vaccine were clustered, and showed lower clinical scores and normal CD4+ counts, whereas 42% of the untreated dogs showed very diminished CD4+ and higher clinical score. The increase in clinical signs of the saline treated group was correlated with an increase in anti-FML antibodies (p < 0.0001), the parasitological evidence ( p = 0.038) and a decrease inLeishmania -specific CD4+ lymphocyte proportions (p = 0.035). These results confirm the immunotherapeutic potential of the enriched-Leishmune ® vaccine. The vaccine reduced the clinical symptoms and evidence of parasite, modulating the outcome of the infection and the dog’s potential infectiosity to phlebotomines. The enriched-Leishmune ® vaccine was subjected to a safety analysis and found to be well tolerated and safept_BR
dc.language.isoen_USpt_BR
dc.subjectImmunotherapypt_BR
dc.subjectLeishmunept_BR
dc.subjectVaccinept_BR
dc.subjectCanine visceral leishmaniasispt_BR
dc.titleImmunotherapy against experimental canine visceral leishmaniasis with the saponin enriched-Leishmune ® vaccine.pt_BR
dc.typeArtigo publicado em periodicopt_BR
dc.rights.licenseO periódico Vaccine concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 3291410128861.-
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