| Literature DB >> 25473035 |
M Teresa Coleman1, Ray Y Chen2, Myungsun Lee3, Philana Ling Lin4, Lori E Dodd5, Pauline Maiello1, Laura E Via2, Youngran Kim3, Gwendolyn Marriner2, Veronique Dartois6, Charles Scanga1, Christopher Janssen7, Jing Wang8, Edwin Klein7, Sang Nae Cho9, Clifton E Barry10, JoAnne L Flynn11.
Abstract
Oxazolidinone antibiotics such as linezolid have shown significant therapeutic effects in patients with extensively drug-resistant (XDR) tuberculosis (TB) despite modest effects in rodents and no demonstrable early bactericidal activity in human phase 2 trials. We show that monotherapy with either linezolid or AZD5847, a second-generation oxazolidinone, reduced bacterial load at necropsy in Mycobacterium tuberculosis-infected cynomolgus macaques with active TB. This effect coincided with a decline in 2-deoxy-2-[(18)F]-fluoro-d-glucose positron emission tomography (FDG PET) imaging avidity in the lungs of these animals and with reductions in pulmonary pathology measured by serial computed tomography (CT) scans over 2 months of monotherapy. In a parallel phase 2 clinical study of linezolid in patients infected with XDR-TB, we also collected PET/CT imaging data from subjects receiving linezolid that had been added to their failing treatment regimens. Quantitative comparisons of PET/CT imaging changes in these human subjects were similar in magnitude to those observed in macaques, demonstrating that the therapeutic effect of these oxazolidinones can be reproduced in this model of experimental chemotherapy. PET/CT imaging may be useful as an early quantitative measure of drug efficacy against TB in human patients.Entities:
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Year: 2014 PMID: 25473035 PMCID: PMC6413515 DOI: 10.1126/scitranslmed.3009500
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956