Glutathione S-transferases of 28kDa as major vaccine candidates against schistosomiasis

For the development of vaccine strategies to generate efficient protection against chronic infections such as parasitic diseases, and more precisely schistosomiasis, controlling pathology could be more relevant than controlling the infection itself. Such strategies, motivated by the need for a cost-effective complement to existing control measures, should focus on parasite molecules involved in fecundity, because in metazoan parasite infections pathology is usually linked to the output of viable eggs. In numerous animal models, vaccination with glutathione S-transferases of 28kDa has been shown to generate an immune response strongly limiting the worm fecundity, in addition to the reduction of the parasite burden. Recent data on acquired immunity directed to 28GST in infected human populations, and new development to draw adapted vaccine formulations, are presented.

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Main Authors: Riveau,Gilles, Poulain-Godefroy,Odile, Dupré,Loïc, Remoué,Franck, Mielcarek,Nathalie, Locht,Camille, Capron,André
Format: Digital revista
Language:English
Published: Instituto Oswaldo Cruz, Ministério da Saúde 1998
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761998000700012
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spelling oai:scielo:S0074-027619980007000122000-07-14Glutathione S-transferases of 28kDa as major vaccine candidates against schistosomiasisRiveau,GillesPoulain-Godefroy,OdileDupré,LoïcRemoué,FranckMielcarek,NathalieLocht,CamilleCapron,André schistosomiasis 28GST vaccine immune response live vectors nucleic acid vaccine For the development of vaccine strategies to generate efficient protection against chronic infections such as parasitic diseases, and more precisely schistosomiasis, controlling pathology could be more relevant than controlling the infection itself. Such strategies, motivated by the need for a cost-effective complement to existing control measures, should focus on parasite molecules involved in fecundity, because in metazoan parasite infections pathology is usually linked to the output of viable eggs. In numerous animal models, vaccination with glutathione S-transferases of 28kDa has been shown to generate an immune response strongly limiting the worm fecundity, in addition to the reduction of the parasite burden. Recent data on acquired immunity directed to 28GST in infected human populations, and new development to draw adapted vaccine formulations, are presented.info:eu-repo/semantics/openAccessInstituto Oswaldo Cruz, Ministério da SaúdeMemórias do Instituto Oswaldo Cruz v.93 suppl.1 19981998-01-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761998000700012en10.1590/S0074-02761998000700012
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libraryname SciELO
language English
format Digital
author Riveau,Gilles
Poulain-Godefroy,Odile
Dupré,Loïc
Remoué,Franck
Mielcarek,Nathalie
Locht,Camille
Capron,André
spellingShingle Riveau,Gilles
Poulain-Godefroy,Odile
Dupré,Loïc
Remoué,Franck
Mielcarek,Nathalie
Locht,Camille
Capron,André
Glutathione S-transferases of 28kDa as major vaccine candidates against schistosomiasis
author_facet Riveau,Gilles
Poulain-Godefroy,Odile
Dupré,Loïc
Remoué,Franck
Mielcarek,Nathalie
Locht,Camille
Capron,André
author_sort Riveau,Gilles
title Glutathione S-transferases of 28kDa as major vaccine candidates against schistosomiasis
title_short Glutathione S-transferases of 28kDa as major vaccine candidates against schistosomiasis
title_full Glutathione S-transferases of 28kDa as major vaccine candidates against schistosomiasis
title_fullStr Glutathione S-transferases of 28kDa as major vaccine candidates against schistosomiasis
title_full_unstemmed Glutathione S-transferases of 28kDa as major vaccine candidates against schistosomiasis
title_sort glutathione s-transferases of 28kda as major vaccine candidates against schistosomiasis
description For the development of vaccine strategies to generate efficient protection against chronic infections such as parasitic diseases, and more precisely schistosomiasis, controlling pathology could be more relevant than controlling the infection itself. Such strategies, motivated by the need for a cost-effective complement to existing control measures, should focus on parasite molecules involved in fecundity, because in metazoan parasite infections pathology is usually linked to the output of viable eggs. In numerous animal models, vaccination with glutathione S-transferases of 28kDa has been shown to generate an immune response strongly limiting the worm fecundity, in addition to the reduction of the parasite burden. Recent data on acquired immunity directed to 28GST in infected human populations, and new development to draw adapted vaccine formulations, are presented.
publisher Instituto Oswaldo Cruz, Ministério da Saúde
publishDate 1998
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02761998000700012
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