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Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model
Cell biology differs between traditional cell culture and 3-dimensional (3-D) systems, and is modulated by the extracellular matrix. Experimentation in 3-D presents challenges, especially with virulent pathogens. Mycobacterium tuberculosis (Mtb) kills more humans than any other infection and is char...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238961/ https://www.ncbi.nlm.nih.gov/pubmed/28063256 http://dx.doi.org/10.7554/eLife.21283 |
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author | Tezera, Liku B Bielecka, Magdalena K Chancellor, Andrew Reichmann, Michaela T Shammari, Basim Al Brace, Patience Batty, Alex Tocheva, Annie Jogai, Sanjay Marshall, Ben G Tebruegge, Marc Jayasinghe, Suwan N Mansour, Salah Elkington, Paul T |
author_facet | Tezera, Liku B Bielecka, Magdalena K Chancellor, Andrew Reichmann, Michaela T Shammari, Basim Al Brace, Patience Batty, Alex Tocheva, Annie Jogai, Sanjay Marshall, Ben G Tebruegge, Marc Jayasinghe, Suwan N Mansour, Salah Elkington, Paul T |
author_sort | Tezera, Liku B |
collection | PubMed |
description | Cell biology differs between traditional cell culture and 3-dimensional (3-D) systems, and is modulated by the extracellular matrix. Experimentation in 3-D presents challenges, especially with virulent pathogens. Mycobacterium tuberculosis (Mtb) kills more humans than any other infection and is characterised by a spatially organised immune response and extracellular matrix remodelling. We developed a 3-D system incorporating virulent mycobacteria, primary human blood mononuclear cells and collagen–alginate matrix to dissect the host-pathogen interaction. Infection in 3-D led to greater cellular survival and permitted longitudinal analysis over 21 days. Key features of human tuberculosis develop, and extracellular matrix integrity favours the host over the pathogen. We optimised multiparameter readouts to study emerging therapeutic interventions: cytokine supplementation, host-directed therapy and immunoaugmentation. Each intervention modulates the host-pathogen interaction, but has both beneficial and harmful effects. This methodology has wide applicability to investigate infectious, inflammatory and neoplastic diseases and develop novel drug regimes and vaccination approaches. DOI: http://dx.doi.org/10.7554/eLife.21283.001 |
format | Online Article Text |
id | pubmed-5238961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52389612017-01-18 Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model Tezera, Liku B Bielecka, Magdalena K Chancellor, Andrew Reichmann, Michaela T Shammari, Basim Al Brace, Patience Batty, Alex Tocheva, Annie Jogai, Sanjay Marshall, Ben G Tebruegge, Marc Jayasinghe, Suwan N Mansour, Salah Elkington, Paul T eLife Immunology Cell biology differs between traditional cell culture and 3-dimensional (3-D) systems, and is modulated by the extracellular matrix. Experimentation in 3-D presents challenges, especially with virulent pathogens. Mycobacterium tuberculosis (Mtb) kills more humans than any other infection and is characterised by a spatially organised immune response and extracellular matrix remodelling. We developed a 3-D system incorporating virulent mycobacteria, primary human blood mononuclear cells and collagen–alginate matrix to dissect the host-pathogen interaction. Infection in 3-D led to greater cellular survival and permitted longitudinal analysis over 21 days. Key features of human tuberculosis develop, and extracellular matrix integrity favours the host over the pathogen. We optimised multiparameter readouts to study emerging therapeutic interventions: cytokine supplementation, host-directed therapy and immunoaugmentation. Each intervention modulates the host-pathogen interaction, but has both beneficial and harmful effects. This methodology has wide applicability to investigate infectious, inflammatory and neoplastic diseases and develop novel drug regimes and vaccination approaches. DOI: http://dx.doi.org/10.7554/eLife.21283.001 eLife Sciences Publications, Ltd 2017-01-07 /pmc/articles/PMC5238961/ /pubmed/28063256 http://dx.doi.org/10.7554/eLife.21283 Text en © 2017, Tezera et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Immunology Tezera, Liku B Bielecka, Magdalena K Chancellor, Andrew Reichmann, Michaela T Shammari, Basim Al Brace, Patience Batty, Alex Tocheva, Annie Jogai, Sanjay Marshall, Ben G Tebruegge, Marc Jayasinghe, Suwan N Mansour, Salah Elkington, Paul T Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model |
title | Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model |
title_full | Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model |
title_fullStr | Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model |
title_full_unstemmed | Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model |
title_short | Dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model |
title_sort | dissection of the host-pathogen interaction in human tuberculosis using a bioengineered 3-dimensional model |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5238961/ https://www.ncbi.nlm.nih.gov/pubmed/28063256 http://dx.doi.org/10.7554/eLife.21283 |
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