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Clofazimine has delayed antimicrobial activity againstMycobacterium tuberculosisbothin vitroandin vivo
Author(s) -
Nicole C. Ammerman,
Rosemary V. Swanson,
Asa Tapley,
Chivonne Moodley,
Bongani Ngcobo,
John Adamson,
Afton Dorasamy,
Sashen Moodley,
Zinhle Mgaga,
Linda A. Bester,
Sanil D. Singh,
Deepak V. Almeida,
J Grosset
Publication year - 2016
Publication title -
journal of antimicrobial chemotherapy
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.124
H-Index - 194
eISSN - 1460-2091
pISSN - 0305-7453
DOI - 10.1093/jac/dkw417
Subject(s) - clofazimine , antimicrobial , in vivo , mycobacterium tuberculosis , pharmacology , isoniazid , microbiology and biotechnology , antibacterial agent , antibiotics , tuberculosis , medicine , in vitro , leprosy , biology , immunology , pathology , biochemistry
The anti-leprosy drug clofazimine has been shown to have antimicrobial activity against Mycobacterium tuberculosis and has been associated with treatment-shortening activity in both clinical and preclinical studies of TB chemotherapy. However, a reported lack of early bactericidal activity (EBA) in TB patients has raised questions regarding the usefulness of clofazimine as an anti-TB drug. Our objective was to systematically evaluate the EBA of clofazimine in vitro and in vivo to provide insight into how and when this drug exerts its antimicrobial activity against M. tuberculosis.

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