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Lactoferrin: A Modulator for Immunity against Tuberculosis Related Granulomatous Pathology

There is great need for a therapeutic that would limit tuberculosis related pathology and thus curtail spread of disease between individuals by establishing a “firebreak” to slow transmission. A promising avenue to increase current therapeutic efficacy may be through incorporation of adjunct compone...

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Detalles Bibliográficos
Autor principal: Actor, Jeffrey K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691619/
https://www.ncbi.nlm.nih.gov/pubmed/26788020
http://dx.doi.org/10.1155/2015/409596
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author Actor, Jeffrey K.
author_facet Actor, Jeffrey K.
author_sort Actor, Jeffrey K.
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description There is great need for a therapeutic that would limit tuberculosis related pathology and thus curtail spread of disease between individuals by establishing a “firebreak” to slow transmission. A promising avenue to increase current therapeutic efficacy may be through incorporation of adjunct components that slow or stop development of aggressive destructive pulmonary pathology. Lactoferrin, an iron-binding glycoprotein found in mucosal secretions and granules of neutrophils, is just such a potential adjunct therapeutic agent. The focus of this review is to explore the utility of lactoferrin to serve as a therapeutic tool to investigate “disruption” of the mycobacterial granuloma. Proposed concepts for mechanisms underlying lactoferrin efficacy to control immunopathology are supported by data generated based on in vivo models using nonpathogenic trehalose 6,6′-dimycolate (TDM, cord factor).
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spelling pubmed-46916192016-01-19 Lactoferrin: A Modulator for Immunity against Tuberculosis Related Granulomatous Pathology Actor, Jeffrey K. Mediators Inflamm Review Article There is great need for a therapeutic that would limit tuberculosis related pathology and thus curtail spread of disease between individuals by establishing a “firebreak” to slow transmission. A promising avenue to increase current therapeutic efficacy may be through incorporation of adjunct components that slow or stop development of aggressive destructive pulmonary pathology. Lactoferrin, an iron-binding glycoprotein found in mucosal secretions and granules of neutrophils, is just such a potential adjunct therapeutic agent. The focus of this review is to explore the utility of lactoferrin to serve as a therapeutic tool to investigate “disruption” of the mycobacterial granuloma. Proposed concepts for mechanisms underlying lactoferrin efficacy to control immunopathology are supported by data generated based on in vivo models using nonpathogenic trehalose 6,6′-dimycolate (TDM, cord factor). Hindawi Publishing Corporation 2015 2015-12-14 /pmc/articles/PMC4691619/ /pubmed/26788020 http://dx.doi.org/10.1155/2015/409596 Text en Copyright © 2015 Jeffrey K. Actor. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Actor, Jeffrey K.
Lactoferrin: A Modulator for Immunity against Tuberculosis Related Granulomatous Pathology
title Lactoferrin: A Modulator for Immunity against Tuberculosis Related Granulomatous Pathology
title_full Lactoferrin: A Modulator for Immunity against Tuberculosis Related Granulomatous Pathology
title_fullStr Lactoferrin: A Modulator for Immunity against Tuberculosis Related Granulomatous Pathology
title_full_unstemmed Lactoferrin: A Modulator for Immunity against Tuberculosis Related Granulomatous Pathology
title_short Lactoferrin: A Modulator for Immunity against Tuberculosis Related Granulomatous Pathology
title_sort lactoferrin: a modulator for immunity against tuberculosis related granulomatous pathology
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4691619/
https://www.ncbi.nlm.nih.gov/pubmed/26788020
http://dx.doi.org/10.1155/2015/409596
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