Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.

The identification of potential vaccine candidates against leptospirosis remains a challenge. However, one such candidate is OmpL37, a potentially surface-exposed antigen that has the highest elastin-binding ability described to date, suggesting that it plays an important role in host colonization....

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Main Authors: Thaís Larré Oliveira, André Alex Grassmann, Rodrigo Andrade Schuch, Amilton Clair Pinto Seixas Neto, Marcelo Mendonça, Daiane Drawanz Hartwig, Alan John Alexander McBride, Odir Antônio Dellagostin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4654524?pdf=render
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spelling doaj-420dc8e5b34d4ba186c360e8a8aa06ba2020-11-25T01:35:14ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-011011e014282110.1371/journal.pone.0142821Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.Thaís Larré OliveiraAndré Alex GrassmannRodrigo Andrade SchuchAmilton Clair Pinto Seixas NetoMarcelo MendonçaDaiane Drawanz HartwigAlan John Alexander McBrideOdir Antônio DellagostinThe identification of potential vaccine candidates against leptospirosis remains a challenge. However, one such candidate is OmpL37, a potentially surface-exposed antigen that has the highest elastin-binding ability described to date, suggesting that it plays an important role in host colonization. In order to evaluate OmpL37's ability to induce a protective immune response, prime-boost, DNA and subunit vaccine strategies were tested in the hamster model of lethal leptospirosis. The humoral immune response was evaluated using an indirect ELISA test, and the cytokine profile in whole blood was determined by quantitative real-time PCR. Unlike the DNA vaccine, the administration of recombinant OmpL37 induced a strong IgG antibody response. When individually administrated, both formulations stimulated a TNF-α mediated inflammatory response. However, none of the OmpL37 formulations or vaccination strategies induced protective immunity. Further studies are required towards the identification of new vaccine targets against leptospirosis.http://europepmc.org/articles/PMC4654524?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Thaís Larré Oliveira
André Alex Grassmann
Rodrigo Andrade Schuch
Amilton Clair Pinto Seixas Neto
Marcelo Mendonça
Daiane Drawanz Hartwig
Alan John Alexander McBride
Odir Antônio Dellagostin
spellingShingle Thaís Larré Oliveira
André Alex Grassmann
Rodrigo Andrade Schuch
Amilton Clair Pinto Seixas Neto
Marcelo Mendonça
Daiane Drawanz Hartwig
Alan John Alexander McBride
Odir Antônio Dellagostin
Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.
PLoS ONE
author_facet Thaís Larré Oliveira
André Alex Grassmann
Rodrigo Andrade Schuch
Amilton Clair Pinto Seixas Neto
Marcelo Mendonça
Daiane Drawanz Hartwig
Alan John Alexander McBride
Odir Antônio Dellagostin
author_sort Thaís Larré Oliveira
title Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.
title_short Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.
title_full Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.
title_fullStr Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.
title_full_unstemmed Evaluation of the Leptospira interrogans Outer Membrane Protein OmpL37 as a Vaccine Candidate.
title_sort evaluation of the leptospira interrogans outer membrane protein ompl37 as a vaccine candidate.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description The identification of potential vaccine candidates against leptospirosis remains a challenge. However, one such candidate is OmpL37, a potentially surface-exposed antigen that has the highest elastin-binding ability described to date, suggesting that it plays an important role in host colonization. In order to evaluate OmpL37's ability to induce a protective immune response, prime-boost, DNA and subunit vaccine strategies were tested in the hamster model of lethal leptospirosis. The humoral immune response was evaluated using an indirect ELISA test, and the cytokine profile in whole blood was determined by quantitative real-time PCR. Unlike the DNA vaccine, the administration of recombinant OmpL37 induced a strong IgG antibody response. When individually administrated, both formulations stimulated a TNF-α mediated inflammatory response. However, none of the OmpL37 formulations or vaccination strategies induced protective immunity. Further studies are required towards the identification of new vaccine targets against leptospirosis.
url http://europepmc.org/articles/PMC4654524?pdf=render
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