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Mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis
Standard treatment for active tuberculosis (TB) requires drug treatment with at least four drugs over six months. Shorter-duration therapy would mean less need for strict adherence, and reduced risk of bacterial resistance. A system pharmacology model of TB infection, and drug therapy was developed...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480878/ https://www.ncbi.nlm.nih.gov/pubmed/32810158 http://dx.doi.org/10.1371/journal.pcbi.1008107 |
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author | Fors, John Strydom, Natasha Fox, William S. Keizer, Ron J. Savic, Radojka M. |
author_facet | Fors, John Strydom, Natasha Fox, William S. Keizer, Ron J. Savic, Radojka M. |
author_sort | Fors, John |
collection | PubMed |
description | Standard treatment for active tuberculosis (TB) requires drug treatment with at least four drugs over six months. Shorter-duration therapy would mean less need for strict adherence, and reduced risk of bacterial resistance. A system pharmacology model of TB infection, and drug therapy was developed and used to simulate the outcome of different drug therapy scenarios. The model incorporated human immune response, granuloma lesions, multi-drug antimicrobial chemotherapy, and bacterial resistance. A dynamic population pharmacokinetic/pharmacodynamic (PK/PD) simulation model including rifampin, isoniazid, pyrazinamide, and ethambutol was developed and parameters aligned with previous experimental data. Population therapy outcomes for simulations were found to be generally consistent with summary results from previous clinical trials, for a range of drug dose and duration scenarios. An online tool developed from this model is released as open source software. The TB simulation tool could support analysis of new therapy options, novel drug types, and combinations, incorporating factors such as patient adherence behavior. |
format | Online Article Text |
id | pubmed-7480878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-74808782020-09-18 Mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis Fors, John Strydom, Natasha Fox, William S. Keizer, Ron J. Savic, Radojka M. PLoS Comput Biol Research Article Standard treatment for active tuberculosis (TB) requires drug treatment with at least four drugs over six months. Shorter-duration therapy would mean less need for strict adherence, and reduced risk of bacterial resistance. A system pharmacology model of TB infection, and drug therapy was developed and used to simulate the outcome of different drug therapy scenarios. The model incorporated human immune response, granuloma lesions, multi-drug antimicrobial chemotherapy, and bacterial resistance. A dynamic population pharmacokinetic/pharmacodynamic (PK/PD) simulation model including rifampin, isoniazid, pyrazinamide, and ethambutol was developed and parameters aligned with previous experimental data. Population therapy outcomes for simulations were found to be generally consistent with summary results from previous clinical trials, for a range of drug dose and duration scenarios. An online tool developed from this model is released as open source software. The TB simulation tool could support analysis of new therapy options, novel drug types, and combinations, incorporating factors such as patient adherence behavior. Public Library of Science 2020-08-18 /pmc/articles/PMC7480878/ /pubmed/32810158 http://dx.doi.org/10.1371/journal.pcbi.1008107 Text en © 2020 Fors et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Fors, John Strydom, Natasha Fox, William S. Keizer, Ron J. Savic, Radojka M. Mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis |
title | Mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis |
title_full | Mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis |
title_fullStr | Mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis |
title_full_unstemmed | Mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis |
title_short | Mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis |
title_sort | mathematical model and tool to explore shorter multi-drug therapy options for active pulmonary tuberculosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7480878/ https://www.ncbi.nlm.nih.gov/pubmed/32810158 http://dx.doi.org/10.1371/journal.pcbi.1008107 |
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