<it>Leishmania infantum HSP70-II</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluation

<p>Abstract</p> <p>Background</p> <p>Visceral leishmaniasis is the most severe form of leishmaniasis and no effective vaccine exists. The use of live attenuated vaccines is emerging as a promising vaccination strategy.</p> <p>Results</p> <p>In th...

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Main Authors: Fresno Manuel, Soto Manuel, Folgueira Cristina, Carrión Javier, Requena Jose M
Format: Article
Language:English
Published: BMC 2011-07-01
Series:Parasites & Vectors
Online Access:http://www.parasitesandvectors.com/content/4/1/150
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spelling doaj-0be9c2fb3b6945b9b775ba9bc9a1f29f2020-11-25T00:37:40ZengBMCParasites & Vectors1756-33052011-07-014115010.1186/1756-3305-4-150<it>Leishmania infantum HSP70-II</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluationFresno ManuelSoto ManuelFolgueira CristinaCarrión JavierRequena Jose M<p>Abstract</p> <p>Background</p> <p>Visceral leishmaniasis is the most severe form of leishmaniasis and no effective vaccine exists. The use of live attenuated vaccines is emerging as a promising vaccination strategy.</p> <p>Results</p> <p>In this study, we tested the ability of a <it>Leishmania infantum </it>deletion mutant, lacking both <it>HSP70-II </it>alleles (ΔHSP70-II), to provide protection against <it>Leishmania </it>infection in the <it>L. major</it>-BALB/c infection model. Administration of the mutant line by either intraperitoneal, intravenous or subcutaneous route invariably leads to the production of high levels of NO and the development in mice of type 1 immune responses, as determined by analysis of anti-<it>Leishmania </it>IgG subclasses. In addition, we have shown that ΔHSP70-II would be a safe live vaccine as immunodeficient SCID mice, and hamsters (<it>Mesocricetus auratus</it>), infected with mutant parasites did not develop any sign of pathology.</p> <p>Conclusions</p> <p>The results suggest that the ΔHSP70-II mutant is a promising and safe vaccine, but further studies in more appropriate animal models (hamsters and dogs) are needed to appraise whether this attenuate mutant would be useful as vaccine against visceral leishmaniasis.</p> http://www.parasitesandvectors.com/content/4/1/150
collection DOAJ
language English
format Article
sources DOAJ
author Fresno Manuel
Soto Manuel
Folgueira Cristina
Carrión Javier
Requena Jose M
spellingShingle Fresno Manuel
Soto Manuel
Folgueira Cristina
Carrión Javier
Requena Jose M
<it>Leishmania infantum HSP70-II</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluation
Parasites & Vectors
author_facet Fresno Manuel
Soto Manuel
Folgueira Cristina
Carrión Javier
Requena Jose M
author_sort Fresno Manuel
title <it>Leishmania infantum HSP70-II</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluation
title_short <it>Leishmania infantum HSP70-II</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluation
title_full <it>Leishmania infantum HSP70-II</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluation
title_fullStr <it>Leishmania infantum HSP70-II</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluation
title_full_unstemmed <it>Leishmania infantum HSP70-II</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluation
title_sort <it>leishmania infantum hsp70-ii</it> null mutant as candidate vaccine against leishmaniasis: a preliminary evaluation
publisher BMC
series Parasites & Vectors
issn 1756-3305
publishDate 2011-07-01
description <p>Abstract</p> <p>Background</p> <p>Visceral leishmaniasis is the most severe form of leishmaniasis and no effective vaccine exists. The use of live attenuated vaccines is emerging as a promising vaccination strategy.</p> <p>Results</p> <p>In this study, we tested the ability of a <it>Leishmania infantum </it>deletion mutant, lacking both <it>HSP70-II </it>alleles (ΔHSP70-II), to provide protection against <it>Leishmania </it>infection in the <it>L. major</it>-BALB/c infection model. Administration of the mutant line by either intraperitoneal, intravenous or subcutaneous route invariably leads to the production of high levels of NO and the development in mice of type 1 immune responses, as determined by analysis of anti-<it>Leishmania </it>IgG subclasses. In addition, we have shown that ΔHSP70-II would be a safe live vaccine as immunodeficient SCID mice, and hamsters (<it>Mesocricetus auratus</it>), infected with mutant parasites did not develop any sign of pathology.</p> <p>Conclusions</p> <p>The results suggest that the ΔHSP70-II mutant is a promising and safe vaccine, but further studies in more appropriate animal models (hamsters and dogs) are needed to appraise whether this attenuate mutant would be useful as vaccine against visceral leishmaniasis.</p>
url http://www.parasitesandvectors.com/content/4/1/150
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