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Therapy for Mycobacterium kansasii Infection: Beyond 2018
The current standard of care therapy for pulmonary Mycobacterium kansasii infection is isoniazid (300 mg/day), rifampin (600 mg/day), and ethambutol (15 mg/kg/day) for 12 months after achieving sputum culture negativity. Rifampin is the key drug in this regimen. The contribution of isoniazid is uncl...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166578/ https://www.ncbi.nlm.nih.gov/pubmed/30319580 http://dx.doi.org/10.3389/fmicb.2018.02271 |
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author | DeStefano, Michelle S. Shoen, Carolyn M. Cynamon, Michael H. |
author_facet | DeStefano, Michelle S. Shoen, Carolyn M. Cynamon, Michael H. |
author_sort | DeStefano, Michelle S. |
collection | PubMed |
description | The current standard of care therapy for pulmonary Mycobacterium kansasii infection is isoniazid (300 mg/day), rifampin (600 mg/day), and ethambutol (15 mg/kg/day) for 12 months after achieving sputum culture negativity. Rifampin is the key drug in this regimen. The contribution of isoniazid is unclear since its in vitro MICs against M. kansasii are near the peak achievable serum levels and more than 100-fold greater than the MICs for Mycobacterium tuberculosis. Ethambutol likely decreases the emergence of rifampin resistant organisms. There are several new drug classes (e.g., quinolones, macrolides, nitroimidazoles, diarylquinolines, and clofazimine) that exhibit antimycobacterial activities against M. tuberculosis but have not yet been adequately studied against M. kansasii infections. The evaluation of in vitro activities of these agents as well as their study in new regimens in comparison to the standard of care regimen in mouse infection models should be undertaken. This knowledge will inform development of human clinical trials of new regimens in comparison to the current standard of care regimen. It is likely that shorter and more effective therapy is achievable with currently available drugs. |
format | Online Article Text |
id | pubmed-6166578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61665782018-10-12 Therapy for Mycobacterium kansasii Infection: Beyond 2018 DeStefano, Michelle S. Shoen, Carolyn M. Cynamon, Michael H. Front Microbiol Microbiology The current standard of care therapy for pulmonary Mycobacterium kansasii infection is isoniazid (300 mg/day), rifampin (600 mg/day), and ethambutol (15 mg/kg/day) for 12 months after achieving sputum culture negativity. Rifampin is the key drug in this regimen. The contribution of isoniazid is unclear since its in vitro MICs against M. kansasii are near the peak achievable serum levels and more than 100-fold greater than the MICs for Mycobacterium tuberculosis. Ethambutol likely decreases the emergence of rifampin resistant organisms. There are several new drug classes (e.g., quinolones, macrolides, nitroimidazoles, diarylquinolines, and clofazimine) that exhibit antimycobacterial activities against M. tuberculosis but have not yet been adequately studied against M. kansasii infections. The evaluation of in vitro activities of these agents as well as their study in new regimens in comparison to the standard of care regimen in mouse infection models should be undertaken. This knowledge will inform development of human clinical trials of new regimens in comparison to the current standard of care regimen. It is likely that shorter and more effective therapy is achievable with currently available drugs. Frontiers Media S.A. 2018-09-24 /pmc/articles/PMC6166578/ /pubmed/30319580 http://dx.doi.org/10.3389/fmicb.2018.02271 Text en Copyright © 2018 DeStefano, Shoen and Cynamon. 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 | Microbiology DeStefano, Michelle S. Shoen, Carolyn M. Cynamon, Michael H. Therapy for Mycobacterium kansasii Infection: Beyond 2018 |
title | Therapy for Mycobacterium kansasii Infection: Beyond 2018 |
title_full | Therapy for Mycobacterium kansasii Infection: Beyond 2018 |
title_fullStr | Therapy for Mycobacterium kansasii Infection: Beyond 2018 |
title_full_unstemmed | Therapy for Mycobacterium kansasii Infection: Beyond 2018 |
title_short | Therapy for Mycobacterium kansasii Infection: Beyond 2018 |
title_sort | therapy for mycobacterium kansasii infection: beyond 2018 |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166578/ https://www.ncbi.nlm.nih.gov/pubmed/30319580 http://dx.doi.org/10.3389/fmicb.2018.02271 |
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