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Intranasal vaccination with killed Leishmania amazonensis promastigotes antigen (LaAg) associated with CAF01 adjuvant induces partial protection in BALB/c mice challenged with Leishmania (infantum) chagasi.

Published online by Cambridge University Press:  23 September 2015

JANINE MIRANDA LEAL
Affiliation:
Núcleo de Doenças Infecciosas/Núcleo de Biotecnologia, Universidade Federal do Espírito Santo – UFES, Vitória, Brazil
MARCELLE MOSQUINI
Affiliation:
Núcleo de Doenças Infecciosas/Núcleo de Biotecnologia, Universidade Federal do Espírito Santo – UFES, Vitória, Brazil
LUCIANA POLACO COVRE
Affiliation:
Núcleo de Doenças Infecciosas/Núcleo de Biotecnologia, Universidade Federal do Espírito Santo – UFES, Vitória, Brazil
NATALY PESCINALLI STAGMILLER
Affiliation:
Núcleo de Núcleo de Biotecnologia, Universidade Federal do Espírito Santo – UFES, Vitória, Brazil
RODRIGO RIBEIRO RODRIGUES
Affiliation:
Núcleo de Doenças Infecciosas/Núcleo de Biotecnologia, Universidade Federal do Espírito Santo – UFES, Vitória, Brazil
DENNIS CHRISTENSEN
Affiliation:
Department of Infectious Disease and Immunology, Statens Serum Institut, Copenhagen, Denmark
HERBERT LEONEL DE MATOS GUEDES
Affiliation:
Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
BARTIRA ROSSI-BERGMANN
Affiliation:
Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
DANIEL CLÁUDIO DE OLIVIERA GOMES*
Affiliation:
Núcleo de Doenças Infecciosas/Núcleo de Biotecnologia, Universidade Federal do Espírito Santo – UFES, Vitória, Brazil Núcleo de Núcleo de Biotecnologia, Universidade Federal do Espírito Santo – UFES, Vitória, Brazil
*
*Corresponding author. Laboratório de Imunobiologia, Núcleo de Doenças Infecciosas/Núcleo de Biotecnologia, Universidade Federal do Espirito Santo – UFES, Av. Marechal Campos, 1468 – Maruípe, Vitória – ES, Cep 29040-091, Brazil. E-mail: dgomes@ndi.ufes.br

Summary

The CAF01 adjuvant has previously been shown to be safe for human use and to be a potent adjuvant for several vaccine antigens. In the present work, we sought to optimize the Leishmania amazonensis antigens (LaAg) intranasal vaccine in an attempt to enhance the protective immune responses against Leishmania (infantum) chagasi by using the CAF01 association. LaAg/CAF01 vaccinated mice that were challenged 15 days after booster dose with L. (infantum) chagasi showed a significant reduction in their parasite burden in both the spleen and liver, which is associated with an increase in specific production of IFN-γ and nitrite, and a decrease in IL-4 production. In addition, LaAg/CAF01 intranasal delivery was able to increase lymphoproliferative immune responses after parasite antigen recall. These results suggest the feasibility of using the intranasal route for the delivery of crude antigens and of a human-compatible adjuvant against visceral leishmaniasis.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2015 

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References

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