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Evaluation of Live Recombinant Nonpathogenic Leishmania Tarentolae Expressing Cysteine Proteinase and A2 Genes As a Candidate Vaccine Against Experimental Canine Visceral Leishmaniasis Publisher Pubmed



Shahbazi M1, 2 ; Zahedifard F1 ; Taheri T1 ; Taslimi Y1 ; Jamshidi S3 ; Shirian S4 ; Mahdavi N3 ; Hassankhani M3 ; Daneshbod Y4 ; Zarkeshesfahani SH2 ; Papadopoulou B5 ; Rafati S1
Authors
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Authors Affiliations
  1. 1. Department of Immunotherapy and Leishmania Vaccine Research, Pasteur Institute of Iran, 69 Pasteur Ave., Tehran, 13164, Iran
  2. 2. Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  3. 3. Department of Internal Medicine, Faculty of Veterinary Medicine, University of Tehran, Tehran, Iran
  4. 4. Department of Molecular and Cytopathology, Daneshbod Pathology Laboratory, Shiraz, Iran
  5. 5. Department of Microbiology, Infectious Disease and Immunology, Research Center in Infectious Diseases, CHU de Quebec Research Center, Laval University, Quebec, QC, Canada

Source: PLoS ONE Published:2015


Abstract

Canine Visceral Leishmaniasis (CVL) is a major veterinary and public health problem caused by Leishmania infantum (L. infantum) in many endemic countries. It is a severe chronic disease with generalized parasite spread to the reticuloendothelial system, such as spleen, liver and bone marrow and is often fatal when left untreated. Control of VL in dogs would dramatically decrease infection pressure of L. infantum for humans, since dogs are the main domestic reservoir. In the past decade, various subunits and DNA antigens have been identified as potential vaccine candidates in experimental animal models, but none has been approved for human use so far. In this study, we vaccinated outbreed dogs with a prime-boost regimen based on recombinant L. tarentolae expressing the L. donovani A2 antigen along with cysteine proteinase genes (CPA and CPB without its unusual C-terminal extension (CPB-CTE) and evaluated its immunogenicity and protective immunity against L. infantum infectious challenge. We showed that vaccinated animals produced significantly higher levels of IgG2, but not IgG1, and also IFN-γ and TNF-α, but low IL-10 levels, before and after challenge as compared to control animals. Protection in dogs was also correlated with a strong DTH response and low parasite burden in the vaccinated group. Altogether, immunization with recombinant L. tarentolae A2-CPA-CPB-CTE was proven to be immunogenic and induced partial protection in dogs, hence representing a promising live vaccine candidate against CVL. © 2015 Shahbazi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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