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      Mycobactericidal Effects of Different Regimens Measured by Molecular Bacterial Load Assay among People Treated for Multidrug-Resistant Tuberculosis in Tanzania

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          Abstract

          Rifampin or multidrug-resistant tuberculosis (RR/MDR-TB) treatment has largely transitioned to regimens free of the injectable aminoglycoside component, despite the drug class’ purported bactericidal activity early in treatment. We tested whether Mycobacterium tuberculosis

          ABSTRACT

          Rifampin or multidrug-resistant tuberculosis (RR/MDR-TB) treatment has largely transitioned to regimens free of the injectable aminoglycoside component, despite the drug class’ purported bactericidal activity early in treatment. We tested whether Mycobacterium tuberculosis killing rates measured by tuberculosis molecular bacterial load assay (TB-MBLA) in sputa correlate with composition of the RR/MDR-TB regimen. Serial sputa were collected from patients with RR/MDR- and drug-sensitive TB at days 0, 3, 7, and 14, and then monthly for 4 months of anti-TB treatment. TB-MBLA was used to quantify viable M. tuberculosis 16S rRNA in sputum for estimation of colony forming units per ml (eCFU/ml). M. tuberculosis killing rates were compared among regimens using nonlinear-mixed-effects modeling of repeated measures. Thirty-seven patients produced 296 serial sputa and received treatment as follows: 13 patients received an injectable bedaquiline-free reference regimen, 9 received an injectable bedaquiline-containing regimen, 8 received an all-oral bedaquiline-based regimen, and 7 patients were treated for drug-sensitive TB with conventional rifampin/isoniazid/pyrazinamide/ethambutol (RHZE). Compared to the adjusted M. tuberculosis killing of −0.17 (95% confidence interval [CI] −0.23 to −0.12) for the injectable bedaquiline-free reference regimen, the killing rates were −0.62 (95% CI −1.05 to −0.20) log 10 eCFU/ml for the injectable bedaquiline-containing regimen ( P = 0.019), −0.35 (95% CI −0.65 to −0.13) log 10 eCFU/ml for the all-oral bedaquiline-based regimen ( P = 0.054), and −0.29 (95% CI −0.78 to +0.22) log 10 eCFU/ml for the RHZE regimen ( P = 0.332). Thus, M. tuberculosis killing rates from sputa were higher among patients who received bedaquiline but were further improved with the addition of an injectable aminoglycoside.

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          Most cited references50

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          Treatment correlates of successful outcomes in pulmonary multidrug-resistant tuberculosis: an individual patient data meta-analysis

          Treatment outcomes for multidrug-resistant tuberculosis remain poor. We aimed to estimate the association of treatment success and death with the use of individual drugs, and the optimal number and duration of treatment with those drugs in patients with multidrug-resistant tuberculosis.
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            Aminoglycosides: An Overview.

            Aminoglycosides are natural or semisynthetic antibiotics derived from actinomycetes. They were among the first antibiotics to be introduced for routine clinical use and several examples have been approved for use in humans. They found widespread use as first-line agents in the early days of antimicrobial chemotherapy, but were eventually replaced in the 1980s with cephalosporins, carbapenems, and fluoroquinolones. Aminoglycosides synergize with a variety of other antibacterial classes, which, in combination with the continued increase in the rise of multidrug-resistant bacteria and the potential to improve the safety and efficacy of the class through optimized dosing regimens, has led to a renewed interest in these broad-spectrum and rapidly bactericidal antibacterials.
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              Four-Month Moxifloxacin-Based Regimens for Drug-Sensitive Tuberculosis

              Early-phase and preclinical studies suggest that moxifloxacin-containing regimens could allow for effective 4-month treatment of uncomplicated, smear-positive pulmonary tuberculosis. We conducted a randomized, double-blind, placebo-controlled, phase 3 trial to test the noninferiority of two moxifloxacin-containing regimens as compared with a control regimen. One group of patients received isoniazid, rifampin, pyrazinamide, and ethambutol for 8 weeks, followed by 18 weeks of isoniazid and rifampin (control group). In the second group, we replaced ethambutol with moxifloxacin for 17 weeks, followed by 9 weeks of placebo (isoniazid group), and in the third group, we replaced isoniazid with moxifloxacin for 17 weeks, followed by 9 weeks of placebo (ethambutol group). The primary end point was treatment failure or relapse within 18 months after randomization. Of the 1931 patients who underwent randomization, in the per-protocol analysis, a favorable outcome was reported in fewer patients in the isoniazid group (85%) and the ethambutol group (80%) than in the control group (92%), for a difference favoring the control group of 6.1 percentage points (97.5% confidence interval [CI], 1.7 to 10.5) versus the isoniazid group and 11.4 percentage points (97.5% CI, 6.7 to 16.1) versus the ethambutol group. Results were consistent in the modified intention-to-treat analysis and all sensitivity analyses. The hazard ratios for the time to culture negativity in both solid and liquid mediums for the isoniazid and ethambutol groups, as compared with the control group, ranged from 1.17 to 1.25, indicating a shorter duration, with the lower bounds of the 95% confidence intervals exceeding 1.00 in all cases. There was no significant difference in the incidence of grade 3 or 4 adverse events, with events reported in 127 patients (19%) in the isoniazid group, 111 (17%) in the ethambutol group, and 123 (19%) in the control group. The two moxifloxacin-containing regimens produced a more rapid initial decline in bacterial load, as compared with the control group. However, noninferiority for these regimens was not shown, which indicates that shortening treatment to 4 months was not effective in this setting. (Funded by the Global Alliance for TB Drug Development and others; REMoxTB ClinicalTrials.gov number, NCT00864383.).
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                Author and article information

                Contributors
                Role: Editor
                Journal
                J Clin Microbiol
                J Clin Microbiol
                jcm
                jcm
                JCM
                Journal of Clinical Microbiology
                American Society for Microbiology (1752 N St., N.W., Washington, DC )
                0095-1137
                1098-660X
                3 February 2021
                19 March 2021
                April 2021
                19 March 2021
                : 59
                : 4
                : e02927-20
                Affiliations
                [a ]Kibong’oto Infectious Diseases Hospital (KIDH), Siha, Kilimanjaro, Tanzania
                [b ]Department of Global Health and Biomedical Sciences, School of Life Sciences and Bioengineering, Nelson Mandela African Institution of Science and Technology (NM-AIST), Arusha, Tanzania
                [c ]National Institute for Medical Research, Mbeya Medical Research Centre, Mbeya, Tanzania
                [d ]Department of Bacteriology, Noguchi Memorial Institute for Medical Research, University of Ghana, Accra, Ghana
                [e ]National Institute for Medical Research, Muhimbili Centre, Dar Es Salaam, Tanzania
                [f ]UCSF Center for Tuberculosis, University of San Francisco, San Francisco, California, USA
                [g ]School of Medicine, University of St Andrews, St. Andrews, Scotland, United Kingdom
                [h ]Division of Infectious Diseases and International Health, University of Virginia, Charlottesville, Virginia, USA
                St. Boniface Hospital
                Author notes
                Address correspondence to Peter M. Mbelele, mbelelepeter@ 123456yahoo.com .

                Citation Mbelele PM, Mpolya EA, Sauli E, Mtafya B, Ntinginya NE, Addo KK, Kreppel K, Mfinanga S, Phillips PPJ, Gillespie SH, Heysell SK, Sabiiti W, Mpagama SG. 2021. Mycobactericidal effects of different regimens measured by molecular bacterial load assay among people treated for multidrug-resistant tuberculosis in Tanzania. J Clin Microbiol 59:e02927-20. https://doi.org/10.1128/JCM.02927-20.

                Author information
                https://orcid.org/0000-0002-2693-187X
                Article
                02927-20
                10.1128/JCM.02927-20
                8092737
                33536294
                31ecee5d-7a15-4b5d-9916-2db1724429af
                Copyright © 2021 Mbelele et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.

                History
                : 19 November 2020
                : 12 January 2021
                : 28 January 2021
                Page count
                Figures: 4, Tables: 4, Equations: 0, References: 50, Pages: 12, Words: 8242
                Funding
                Funded by: DELTAS Africa Initiative;
                Award ID: Afrique One-ASPIRE /DEL-15-008
                Award Recipient :
                Funded by: DELTA Africa Initiative;
                Award ID: Afrique One-ASPIRE /DEL-15-008
                Award Recipient :
                Funded by: DELTA Africa Initiative;
                Award ID: Afrique One-ASPIRE /DEL-15-008
                Award Recipient :
                Funded by: European and Developing Countries Clinical Trials Partnership (EDCTP), https://doi.org/10.13039/501100001713;
                Award ID: TMA2016SF-1463-REMODELTZ
                Award Recipient :
                Funded by: European and Developing Countries Clinical Trials Partnership (EDCTP), https://doi.org/10.13039/501100001713;
                Award ID: TMA2016SF-1463-REMODELTZ
                Award Recipient :
                Categories
                Mycobacteriology and Aerobic Actinomycetes
                Custom metadata
                April 2021

                Microbiology & Virology
                kibong'oto,tanzania,mdr-tb treatment regimens,molecular bacterial load assay,multidrug-resistant tb,mycobactericidal effects,mycobacterium tuberculosis,all-oral bedaquiline regimen,injectable aminoglycoside regimen

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