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A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction?

Leptospirosis is the most widespread zoonosis in the world and a neglected tropical disease estimated to cause severe infection in more than one million people worldwide every year that can be combated by effective immunization. However, no significant progress has been made on the leptospirosis vac...

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Autores principales: Grassmann, André Alex, Souza, Jéssica Dias, McBride, Alan John Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343615/
https://www.ncbi.nlm.nih.gov/pubmed/28337203
http://dx.doi.org/10.3389/fimmu.2017.00256
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author Grassmann, André Alex
Souza, Jéssica Dias
McBride, Alan John Alexander
author_facet Grassmann, André Alex
Souza, Jéssica Dias
McBride, Alan John Alexander
author_sort Grassmann, André Alex
collection PubMed
description Leptospirosis is the most widespread zoonosis in the world and a neglected tropical disease estimated to cause severe infection in more than one million people worldwide every year that can be combated by effective immunization. However, no significant progress has been made on the leptospirosis vaccine since the advent of bacterins over 100 years. Although protective against lethal infection, particularly in animals, bacterin-induced immunity is considered short term, serovar restricted, and the vaccine can cause serious side effects. The urgent need for a new vaccine has motivated several research groups to evaluate the protective immune response induced by recombinant vaccines. Significant protection has been reported with several promising outer membrane proteins, including LipL32 and the leptospiral immunoglobulin-like proteins. However, efficacy was variable and failed to induce a cross-protective response or sterile immunity among vaccinated animals. As hundreds of draft genomes of all known Leptospira species are now available, this should aid novel target discovery through reverse vaccinology (RV) and pangenomic studies. The identification of surface-exposed vaccine candidates that are highly conserved among infectious Leptospira spp. is a requirement for the development of a cross-protective universal vaccine. However, the lack of immune correlates is a major drawback to the application of RV to Leptospira genomes. In addition, as the protective immune response against leptospirosis is not fully understood, the rational use of adjuvants tends to be a process of trial and error. In this perspective, we discuss current advances, the pitfalls, and possible solutions for the development of a universal leptospirosis vaccine.
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spelling pubmed-53436152017-03-23 A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction? Grassmann, André Alex Souza, Jéssica Dias McBride, Alan John Alexander Front Immunol Immunology Leptospirosis is the most widespread zoonosis in the world and a neglected tropical disease estimated to cause severe infection in more than one million people worldwide every year that can be combated by effective immunization. However, no significant progress has been made on the leptospirosis vaccine since the advent of bacterins over 100 years. Although protective against lethal infection, particularly in animals, bacterin-induced immunity is considered short term, serovar restricted, and the vaccine can cause serious side effects. The urgent need for a new vaccine has motivated several research groups to evaluate the protective immune response induced by recombinant vaccines. Significant protection has been reported with several promising outer membrane proteins, including LipL32 and the leptospiral immunoglobulin-like proteins. However, efficacy was variable and failed to induce a cross-protective response or sterile immunity among vaccinated animals. As hundreds of draft genomes of all known Leptospira species are now available, this should aid novel target discovery through reverse vaccinology (RV) and pangenomic studies. The identification of surface-exposed vaccine candidates that are highly conserved among infectious Leptospira spp. is a requirement for the development of a cross-protective universal vaccine. However, the lack of immune correlates is a major drawback to the application of RV to Leptospira genomes. In addition, as the protective immune response against leptospirosis is not fully understood, the rational use of adjuvants tends to be a process of trial and error. In this perspective, we discuss current advances, the pitfalls, and possible solutions for the development of a universal leptospirosis vaccine. Frontiers Media S.A. 2017-03-09 /pmc/articles/PMC5343615/ /pubmed/28337203 http://dx.doi.org/10.3389/fimmu.2017.00256 Text en Copyright © 2017 Grassmann, Souza and McBride. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Grassmann, André Alex
Souza, Jéssica Dias
McBride, Alan John Alexander
A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction?
title A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction?
title_full A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction?
title_fullStr A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction?
title_full_unstemmed A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction?
title_short A Universal Vaccine against Leptospirosis: Are We Going in the Right Direction?
title_sort universal vaccine against leptospirosis: are we going in the right direction?
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343615/
https://www.ncbi.nlm.nih.gov/pubmed/28337203
http://dx.doi.org/10.3389/fimmu.2017.00256
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