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Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity

While tuberculosis continues to afflict mankind, the immunological mechanisms underlying TB disease development are still incompletely understood. Advanced preclinical models for TB research include both rhesus and cynomolgus macaques (Macaca mulatta and Macaca fascicularis, respectively), with rhes...

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Autores principales: Dijkman, Karin, Vervenne, Richard A. W., Sombroek, Claudia C., Boot, Charelle, Hofman, Sam O., van Meijgaarden, Krista E., Ottenhoff, Tom H. M., Kocken, Clemens H. M., Haanstra, Krista G., Vierboom, Michel P. M., Verreck, Frank A. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838139/
https://www.ncbi.nlm.nih.gov/pubmed/31736945
http://dx.doi.org/10.3389/fimmu.2019.02479
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author Dijkman, Karin
Vervenne, Richard A. W.
Sombroek, Claudia C.
Boot, Charelle
Hofman, Sam O.
van Meijgaarden, Krista E.
Ottenhoff, Tom H. M.
Kocken, Clemens H. M.
Haanstra, Krista G.
Vierboom, Michel P. M.
Verreck, Frank A. W.
author_facet Dijkman, Karin
Vervenne, Richard A. W.
Sombroek, Claudia C.
Boot, Charelle
Hofman, Sam O.
van Meijgaarden, Krista E.
Ottenhoff, Tom H. M.
Kocken, Clemens H. M.
Haanstra, Krista G.
Vierboom, Michel P. M.
Verreck, Frank A. W.
author_sort Dijkman, Karin
collection PubMed
description While tuberculosis continues to afflict mankind, the immunological mechanisms underlying TB disease development are still incompletely understood. Advanced preclinical models for TB research include both rhesus and cynomolgus macaques (Macaca mulatta and Macaca fascicularis, respectively), with rhesus typically being more susceptible to acute progressive TB disease than cynomolgus macaques. To determine which immune mechanisms are responsible for this dissimilar disease development, we profiled a broad range of innate and adaptive responses, both local and peripheral, following experimental pulmonary Mycobacterium tuberculosis (Mtb) infection of both species. While T-cell and antibody responses appeared indistinguishable, we identified anti-inflammatory skewing of peripheral monocytes in rhesus and a more prominent local pro-inflammatory cytokine release profile in cynomolgus macaques associated with divergent TB disease outcome. Importantly, these differences were detectable both before and early after infection. This work shows that inflammatory and innate immune status prior to and at early stages after infection, critically affects outcome of TB infection.
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spelling pubmed-68381392019-11-15 Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity Dijkman, Karin Vervenne, Richard A. W. Sombroek, Claudia C. Boot, Charelle Hofman, Sam O. van Meijgaarden, Krista E. Ottenhoff, Tom H. M. Kocken, Clemens H. M. Haanstra, Krista G. Vierboom, Michel P. M. Verreck, Frank A. W. Front Immunol Immunology While tuberculosis continues to afflict mankind, the immunological mechanisms underlying TB disease development are still incompletely understood. Advanced preclinical models for TB research include both rhesus and cynomolgus macaques (Macaca mulatta and Macaca fascicularis, respectively), with rhesus typically being more susceptible to acute progressive TB disease than cynomolgus macaques. To determine which immune mechanisms are responsible for this dissimilar disease development, we profiled a broad range of innate and adaptive responses, both local and peripheral, following experimental pulmonary Mycobacterium tuberculosis (Mtb) infection of both species. While T-cell and antibody responses appeared indistinguishable, we identified anti-inflammatory skewing of peripheral monocytes in rhesus and a more prominent local pro-inflammatory cytokine release profile in cynomolgus macaques associated with divergent TB disease outcome. Importantly, these differences were detectable both before and early after infection. This work shows that inflammatory and innate immune status prior to and at early stages after infection, critically affects outcome of TB infection. Frontiers Media S.A. 2019-11-01 /pmc/articles/PMC6838139/ /pubmed/31736945 http://dx.doi.org/10.3389/fimmu.2019.02479 Text en Copyright © 2019 Dijkman, Vervenne, Sombroek, Boot, Hofman, van Meijgaarden, Ottenhoff, Kocken, Haanstra, Vierboom and Verreck. 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) and the copyright owner(s) 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
Dijkman, Karin
Vervenne, Richard A. W.
Sombroek, Claudia C.
Boot, Charelle
Hofman, Sam O.
van Meijgaarden, Krista E.
Ottenhoff, Tom H. M.
Kocken, Clemens H. M.
Haanstra, Krista G.
Vierboom, Michel P. M.
Verreck, Frank A. W.
Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity
title Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity
title_full Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity
title_fullStr Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity
title_full_unstemmed Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity
title_short Disparate Tuberculosis Disease Development in Macaque Species Is Associated With Innate Immunity
title_sort disparate tuberculosis disease development in macaque species is associated with innate immunity
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838139/
https://www.ncbi.nlm.nih.gov/pubmed/31736945
http://dx.doi.org/10.3389/fimmu.2019.02479
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