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Improving treatment outcome assessment in a mouse tuberculosis model

Preclinical treatment outcome evaluation of tuberculosis (TB) occurs primarily in mice. Current designs compare relapse rates of different regimens at selected time points, but lack information about the correlation between treatment length and treatment outcome, which is required to efficiently est...

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Autores principales: Mourik, Bas C., Svensson, Robin J., de Knegt, Gerjo J., Bax, Hannelore I., Verbon, Annelies, Simonsson, Ulrika S. H., de Steenwinkel, Jurriaan E. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890284/
https://www.ncbi.nlm.nih.gov/pubmed/29632372
http://dx.doi.org/10.1038/s41598-018-24067-x
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author Mourik, Bas C.
Svensson, Robin J.
de Knegt, Gerjo J.
Bax, Hannelore I.
Verbon, Annelies
Simonsson, Ulrika S. H.
de Steenwinkel, Jurriaan E. M.
author_facet Mourik, Bas C.
Svensson, Robin J.
de Knegt, Gerjo J.
Bax, Hannelore I.
Verbon, Annelies
Simonsson, Ulrika S. H.
de Steenwinkel, Jurriaan E. M.
author_sort Mourik, Bas C.
collection PubMed
description Preclinical treatment outcome evaluation of tuberculosis (TB) occurs primarily in mice. Current designs compare relapse rates of different regimens at selected time points, but lack information about the correlation between treatment length and treatment outcome, which is required to efficiently estimate a regimens’ treatment-shortening potential. Therefore we developed a new approach. BALB/c mice were infected with a Mycobacterium tuberculosis Beijing genotype strain and were treated with rifapentine-pyrazinamide-isoniazid-ethambutol (R(p)ZHE), rifampicin-pyrazinamide-moxifloxacin-ethambutol (RZME) or rifampicin-pyrazinamide-moxifloxacin-isoniazid (RZMH). Treatment outcome was assessed in n = 3 mice after 9 different treatment lengths between 2–6 months. Next, we created a mathematical model that best fitted the observational data and used this for inter-regimen comparison. The observed data were best described by a sigmoidal E(max) model in favor over linear or conventional E(max) models. Estimating regimen-specific parameters showed significantly higher curative potentials for RZME and R(p)ZHE compared to RZMH. In conclusion, we provide a new design for treatment outcome evaluation in a mouse TB model, which (i) provides accurate tools for assessment of the relationship between treatment length and predicted cure, (ii) allows for efficient comparison between regimens and (iii) adheres to the reduction and refinement principles of laboratory animal use.
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spelling pubmed-58902842018-04-13 Improving treatment outcome assessment in a mouse tuberculosis model Mourik, Bas C. Svensson, Robin J. de Knegt, Gerjo J. Bax, Hannelore I. Verbon, Annelies Simonsson, Ulrika S. H. de Steenwinkel, Jurriaan E. M. Sci Rep Article Preclinical treatment outcome evaluation of tuberculosis (TB) occurs primarily in mice. Current designs compare relapse rates of different regimens at selected time points, but lack information about the correlation between treatment length and treatment outcome, which is required to efficiently estimate a regimens’ treatment-shortening potential. Therefore we developed a new approach. BALB/c mice were infected with a Mycobacterium tuberculosis Beijing genotype strain and were treated with rifapentine-pyrazinamide-isoniazid-ethambutol (R(p)ZHE), rifampicin-pyrazinamide-moxifloxacin-ethambutol (RZME) or rifampicin-pyrazinamide-moxifloxacin-isoniazid (RZMH). Treatment outcome was assessed in n = 3 mice after 9 different treatment lengths between 2–6 months. Next, we created a mathematical model that best fitted the observational data and used this for inter-regimen comparison. The observed data were best described by a sigmoidal E(max) model in favor over linear or conventional E(max) models. Estimating regimen-specific parameters showed significantly higher curative potentials for RZME and R(p)ZHE compared to RZMH. In conclusion, we provide a new design for treatment outcome evaluation in a mouse TB model, which (i) provides accurate tools for assessment of the relationship between treatment length and predicted cure, (ii) allows for efficient comparison between regimens and (iii) adheres to the reduction and refinement principles of laboratory animal use. Nature Publishing Group UK 2018-04-09 /pmc/articles/PMC5890284/ /pubmed/29632372 http://dx.doi.org/10.1038/s41598-018-24067-x Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mourik, Bas C.
Svensson, Robin J.
de Knegt, Gerjo J.
Bax, Hannelore I.
Verbon, Annelies
Simonsson, Ulrika S. H.
de Steenwinkel, Jurriaan E. M.
Improving treatment outcome assessment in a mouse tuberculosis model
title Improving treatment outcome assessment in a mouse tuberculosis model
title_full Improving treatment outcome assessment in a mouse tuberculosis model
title_fullStr Improving treatment outcome assessment in a mouse tuberculosis model
title_full_unstemmed Improving treatment outcome assessment in a mouse tuberculosis model
title_short Improving treatment outcome assessment in a mouse tuberculosis model
title_sort improving treatment outcome assessment in a mouse tuberculosis model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5890284/
https://www.ncbi.nlm.nih.gov/pubmed/29632372
http://dx.doi.org/10.1038/s41598-018-24067-x
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