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TLR Agonists as Modulators of the Innate Immune Response and Their Potential as Agents Against Infectious Disease

Immunotherapies that can either activate or suppress innate immune responses are being investigated as treatments against infectious diseases and the pathology they can cause. The objective of these therapies is to elicit protective immune responses thereby limiting the harm inflicted by the pathoge...

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Detalles Bibliográficos
Autores principales: Mifsud, Edin J., Tan, Amabel C. L., Jackson, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939722/
https://www.ncbi.nlm.nih.gov/pubmed/24624130
http://dx.doi.org/10.3389/fimmu.2014.00079
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author Mifsud, Edin J.
Tan, Amabel C. L.
Jackson, David C.
author_facet Mifsud, Edin J.
Tan, Amabel C. L.
Jackson, David C.
author_sort Mifsud, Edin J.
collection PubMed
description Immunotherapies that can either activate or suppress innate immune responses are being investigated as treatments against infectious diseases and the pathology they can cause. The objective of these therapies is to elicit protective immune responses thereby limiting the harm inflicted by the pathogen. The Toll-like receptor (TLR) signaling pathway plays critical roles in numerous host immune defenses and has been identified as an immunotherapeutic target against the consequences of infectious challenge. This review focuses on some of the recent advances being made in the development of TLR-ligands as potential prophylactic and/or therapeutic agents.
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spelling pubmed-39397222014-03-12 TLR Agonists as Modulators of the Innate Immune Response and Their Potential as Agents Against Infectious Disease Mifsud, Edin J. Tan, Amabel C. L. Jackson, David C. Front Immunol Immunology Immunotherapies that can either activate or suppress innate immune responses are being investigated as treatments against infectious diseases and the pathology they can cause. The objective of these therapies is to elicit protective immune responses thereby limiting the harm inflicted by the pathogen. The Toll-like receptor (TLR) signaling pathway plays critical roles in numerous host immune defenses and has been identified as an immunotherapeutic target against the consequences of infectious challenge. This review focuses on some of the recent advances being made in the development of TLR-ligands as potential prophylactic and/or therapeutic agents. Frontiers Media S.A. 2014-03-03 /pmc/articles/PMC3939722/ /pubmed/24624130 http://dx.doi.org/10.3389/fimmu.2014.00079 Text en Copyright © 2014 Mifsud, Tan and Jackson. http://creativecommons.org/licenses/by/3.0/ 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
Mifsud, Edin J.
Tan, Amabel C. L.
Jackson, David C.
TLR Agonists as Modulators of the Innate Immune Response and Their Potential as Agents Against Infectious Disease
title TLR Agonists as Modulators of the Innate Immune Response and Their Potential as Agents Against Infectious Disease
title_full TLR Agonists as Modulators of the Innate Immune Response and Their Potential as Agents Against Infectious Disease
title_fullStr TLR Agonists as Modulators of the Innate Immune Response and Their Potential as Agents Against Infectious Disease
title_full_unstemmed TLR Agonists as Modulators of the Innate Immune Response and Their Potential as Agents Against Infectious Disease
title_short TLR Agonists as Modulators of the Innate Immune Response and Their Potential as Agents Against Infectious Disease
title_sort tlr agonists as modulators of the innate immune response and their potential as agents against infectious disease
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939722/
https://www.ncbi.nlm.nih.gov/pubmed/24624130
http://dx.doi.org/10.3389/fimmu.2014.00079
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