Title
Immunogenicity and protective efficacy of a new Leishmania hypothetical protein applied as a DNA vaccine or in a recombinant form against Leishmania infantum infection
Date Issued
01 February 2019
Access level
metadata only access
Resource Type
journal article
Author(s)
Ribeiro P.A.F.
Dias D.S.
Lage D.P.
Martins V.T.
Costa L.E.
Santos T.T.O.
Ramos F.F.
Tavares G.S.V.
Mendonça D.V.C.
Ludolf F.
Gomes D.A.
Rodrigues M.A.
Silva E.S.
Galdino A.S.
Duarte M.C.
Roatt B.M.
Menezes-Souza D.
Teixeira A.L.
Coelho E.A.F.
Publisher(s)
Elsevier Ltd
Abstract
Vaccination is one the most important strategies for the prevention of visceral leishmaniasis (VL). In the current study, a new Leishmania hypothetical protein, LiHyP, which was previously showed as antigenic in an immunoproteomic search in canine VL, was evaluated regarding its immunogenicity and protective efficacy against Leishmania infantum infection. The effects of the immunization using LiHyP were evaluated when administered as a DNA plasmid (DNA LiHyP) or recombinant protein (rLiHyP) associated with saponin. The immunity elicited by both vaccination regimens reduced the parasitism in liver, spleen, bone marrow and draining lymph nodes, being associated with high levels of IFN-γ IL-12, GM-CSF, and specific IgG2a antibody, besides low production of IL-4, IL-10, and protein and parasite-specific IgG1 antibodies. CD4 + T cells contributed more significantly to IFN-γ production in the rLiHyP/saponin group, while CD8 + T cells were more important in the production of this cytokine in the DNA LiHyP group. In addition, increased IFN-γ secretion, along with low levels of IL-10, were found when PBMCs from treated VL subject and healthy individuals were stimulated with the recombinant protein. In conclusion, when administered either as a DNA plasmid or recombinant protein, LiHyP can direct the immune response towards a Th1 immune profile, protecting animals against L. infantum infection; therefore, it can be seen as a promising immunogen against human VL.
Start page
108
End page
118
Volume
106
Language
English
OCDE Knowledge area
Inmunología Tecnología para la identificación y funcionamiento del ADN, proteínas y enzimas y como influencian la enfermedad) Enfermedades infecciosas
Scopus EID
2-s2.0-85059186392
PubMed ID
Source
Molecular Immunology
ISSN of the container
01615890
Sponsor(s)
This work was supported by grants from FAPEMIG ( CBB-APQ-00819-12 and CBB-APQ-01778-2014 ) and CNPq ( APQ-482976/2012-8 , APQ-488237/2013-0 , and APQ-467640/2014-9 ). MACF is a grant recipient of FAPEMIG/CAPES. EAFC, DMS and ALT are grants recipient of CNPq. The authors would like thank the CAPI (Image Acquisition and Processing Center), from ICB, UFMG; where microscopic data showed in this work were obtained.
Sources of information: Directorio de Producción Científica Scopus