DC Field | Value | Language |
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dc.contributor.author | J M Lee | - |
dc.contributor.author | J Park | - |
dc.contributor.author | S Choi | - |
dc.contributor.author | B W Jhun | - |
dc.contributor.author | S Y Kim | - |
dc.contributor.author | K W Jo | - |
dc.contributor.author | Jung Joo Hong | - |
dc.contributor.author | L H Kim | - |
dc.contributor.author | S J Shin | - |
dc.date.accessioned | 2021-01-27T03:30:37Z | - |
dc.date.available | 2021-01-27T03:30:37Z | - |
dc.date.issued | 2021 | - |
dc.identifier.issn | 1664-302x | - |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/24035 | - |
dc.description.abstract | Treatment outcomes using the standard regimen (a macrolide, ethambutol, and rifampicin) for Mycobacterium avium complex-pulmonary disease (MAC-PD) remain unsatisfactory. Thus, improved treatment regimens for MAC-PD are required. Clofazimine has recently been revisited as an effective drug against mycobacterial infection. We performed a comparison between the standard regimen and an alternative regimen (replacing the rifampicin of the standard regimen with clofazimine) based on the intracellular anti-MAC activities of the individual drugs in a murine model of chronic progressive MAC-pulmonary infection (MAC-PI). The intracellular anti-MAC activities of the individual drugs and their combinations in murine bone marrow-derived macrophages (BMDMs) were determined. The treatment efficacies of the standard and clofazimine-containing regimens were evaluated in mice chronically infected with M. avium by initiating 2- and 4-week treatment at 8 weeks post-infection. Bacterial loads in the lung, spleen, and liver were assessed along with lung inflammation. Insufficient intracellular anti-MAC activity of rifampicin in BMDMs was recorded despite its low in vitro minimum inhibitory concentrations (MICs), whereas optimal intracellular killing activity against all tested MAC strains was achieved with clofazimine. Compared to the standard regimen, the clofazimine-containing regimen significantly reduced CFUs in all organs and achieved marked reductions in lung inflammation. The replacement of rifampicin with clofazimine in the treatment regimen resulted in more favorable outcomes in an animal model of chronic progressive MAC-PI. Intriguingly, 2 weeks of treatment with the clofazimine-containing regimen reduced bacterial loads more effectively than 4 weeks of treatment with the standard regimen in M. avium-infected mice. Thus, the clofazimine-containing regimen also had a treatment-shortening effect. | - |
dc.publisher | Frontiers Media Sa | - |
dc.title | A clofazimine-containing regimen confers improved treatment outcomes in macrophages and in a murine model of chronic progressive pulmonary infection caused by the Mycobacterium avium complex | - |
dc.title.alternative | A clofazimine-containing regimen confers improved treatment outcomes in macrophages and in a murine model of chronic progressive pulmonary infection caused by the Mycobacterium avium complex | - |
dc.type | Article | - |
dc.citation.title | Frontiers in Microbiology | - |
dc.citation.number | 0 | - |
dc.citation.endPage | 626216 | - |
dc.citation.startPage | 626216 | - |
dc.citation.volume | 11 | - |
dc.contributor.affiliatedAuthor | Jung Joo Hong | - |
dc.contributor.alternativeName | 이주미 | - |
dc.contributor.alternativeName | 박지윤 | - |
dc.contributor.alternativeName | 최상원 | - |
dc.contributor.alternativeName | 전병우 | - |
dc.contributor.alternativeName | 김수영 | - |
dc.contributor.alternativeName | 조경욱 | - |
dc.contributor.alternativeName | 홍정주 | - |
dc.contributor.alternativeName | 김이한 | - |
dc.contributor.alternativeName | 신성재 | - |
dc.identifier.bibliographicCitation | Frontiers in Microbiology, vol. 11, pp. 626216-626216 | - |
dc.identifier.doi | 10.3389/fmicb.2020.626216 | - |
dc.subject.keyword | Mycobacterium avium complex-pulmonary disease | - |
dc.subject.keyword | Clofazimine | - |
dc.subject.keyword | Clofazimine-containing regimen | - |
dc.subject.keyword | Standard treatment regimen | - |
dc.subject.keyword | Minimum inhibitory concentrations | - |
dc.subject.keyword | Intracellular drug susceptibility test: In vivo drug susceptibility test | - |
dc.subject.keyword | Chronic progressive murine model | - |
dc.subject.local | Mycobacterium avium complex-pulmonary disease | - |
dc.subject.local | Clofazimine | - |
dc.subject.local | Clofazimine-containing regimen | - |
dc.subject.local | Standard treatment regimen | - |
dc.subject.local | Minimum inhibitory concentration (MIC) | - |
dc.subject.local | Minimum inhibitory concentrations | - |
dc.subject.local | Intracellular drug susceptibility test: In vivo drug susceptibility test | - |
dc.subject.local | Chronic progressive murine model | - |
dc.description.journalClass | Y | - |
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