Functional, biochemical and 3D studies of Mycobacterium tuberculosis protein peptides for an effective anti-tuberculosis vaccine

Tuberculosis (TB) is an air-born, transmissible disease, having an estimated 9.4 million new TB cases worldwide in 2009. Eventual control of this disease by developing a safe and efficient new vaccine able to detain its spread will have an enormous impact on public health policy. Selecting potential...

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Autores:
Tipo de recurso:
Fecha de publicación:
2014
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/23782
Acceso en línea:
https://doi.org/10.3109/1040841X.2013.763221
https://repository.urosario.edu.co/handle/10336/23782
Palabra clave:
Bacterial antigen
Bacterial protein
Bcg vaccine
Rv 0180 c protein
Rv 0227 c protein
Rv 0679 c protein
Rv 1490 protein
Rv 1510 c protein
Rv 1980 c protein
Rv 2004 c protein
Rv 2301 protein
Rv 2536 protein
Rv 2560 protein
Rv 2707 protein
Rv 2969c protein
Rv 3166 c protein
Rv 3481 c protein
Rv 3629 c protein
Rv 3630 protein
Rv 3804 c protein
Rv 3910 protein
Synthetic peptide
Unclassified drug
Bioinformatics
Immune response
Molecular biology
Mycobacterium tuberculosis
Nonhuman
Priority journal
Protein analysis
Protein binding
Protein function
Proteomics
Review
Three dimensional imaging
Bacterial adhesion
Bacterial proteins
Cell line
Epithelial cells
Humans
Macrophages
Mycobacterium tuberculosis
Tuberculosis vaccines
Mycobacterium tuberculosis surface protein
Receptor-ligand interaction
Subunit-vaccine
Synthetic-peptides
bacterial
Antigens
Rights
License
Abierto (Texto Completo)
Description
Summary:Tuberculosis (TB) is an air-born, transmissible disease, having an estimated 9.4 million new TB cases worldwide in 2009. Eventual control of this disease by developing a safe and efficient new vaccine able to detain its spread will have an enormous impact on public health policy. Selecting potential antigens to be included in a multi-epitope, minimal subunit-based, chemically-synthesized vaccine containing the minimum sequences needed for blocking mycobacterial interaction with host cells is a complex task due to the multiple mechanisms involved in M. tuberculosis infection and the mycobacterium's immune evasion mechanisms. Our methodology, described here takes into account a highly robust, specific, sensitive and functional approach to the search for potential epitopes to be included in an anti-TB vaccine; it has been based on identifying short mycobacterial protein fragments using synthetic peptides having high affinity interaction with alveolar epithelial cells (A549) and monocyte-derived macrophages (U937) which are able to block the microorganism's entry to target cells in in vitro assays. This manuscript presents a review of the results obtained with some of the MTB H37Rv proteins studied to date, aimed at using these high activity binding peptides (HABPs) as platforms to be included in a minimal subunit-based, multiepitope, chemically-synthesized, antituberculosis vaccine. © 2014 Informa Healthcare USA, Inc. All rights reserved: reproduction in whole or part not permitted.