Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783312844643631104 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5890284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mourikbasc improvingtreatmentoutcomeassessmentinamousetuberculosismodel AT svenssonrobinj improvingtreatmentoutcomeassessmentinamousetuberculosismodel AT deknegtgerjoj improvingtreatmentoutcomeassessmentinamousetuberculosismodel AT baxhannelorei improvingtreatmentoutcomeassessmentinamousetuberculosismodel AT verbonannelies improvingtreatmentoutcomeassessmentinamousetuberculosismodel AT simonssonulrikash improvingtreatmentoutcomeassessmentinamousetuberculosismodel AT desteenwinkeljurriaanem improvingtreatmentoutcomeassessmentinamousetuberculosismodel |