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PET/CT imaging reveals a therapeutic response to oxazolidinones in macaques and humans with tuberculosis.
Coleman, M Teresa; Chen, Ray Y; Lee, Myungsun; Lin, Philana Ling; Dodd, Lori E; Maiello, Pauline; Via, Laura E; Kim, Youngran; Marriner, Gwendolyn; Dartois, Veronique; Scanga, Charles; Janssen, Christopher; Wang, Jing; Klein, Edwin; Cho, Sang Nae; Barry, Clifton E; Flynn, JoAnne L.
Affiliation
  • Coleman MT; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15260, USA.
  • Chen RY; Tuberculosis Research Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD 20892, USA.
  • Lee M; International Tuberculosis Research Center, Changwon 631-710, Republic of Korea.
  • Lin PL; Department of Pediatrics, Children's Hospital of Pittsburgh of the University of Pittsburgh Medical Center, Pittsburgh, PA 15260, USA.
  • Dodd LE; Biostatistics Research Branch, NIAID, NIH, Bethesda, MD 20892, USA.
  • Maiello P; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15260, USA.
  • Via LE; Tuberculosis Research Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD 20892, USA.
  • Kim Y; International Tuberculosis Research Center, Changwon 631-710, Republic of Korea.
  • Marriner G; Tuberculosis Research Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD 20892, USA.
  • Dartois V; Public Health Research Institute Center, Rutgers New Jersey Medical School, Newark, NJ 07103, USA.
  • Scanga C; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15260, USA.
  • Janssen C; Division of Laboratory Animal Resources, University of Pittsburgh, Pittsburgh, PA 15260, USA.
  • Wang J; Clinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research Inc., Frederick National Laboratory for Cancer Research, Frederick, MD 21701, USA.
  • Klein E; Division of Laboratory Animal Resources, University of Pittsburgh, Pittsburgh, PA 15260, USA.
  • Cho SN; International Tuberculosis Research Center, Changwon 631-710, Republic of Korea. Department of Microbiology, Yonsei University College of Medicine, Seoul 120-752, Republic of Korea.
  • Barry CE; Tuberculosis Research Section, Laboratory of Clinical Infectious Diseases, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD 20892, USA. Institute of Infectious Disease and Molecular Medicine, and the Department of Clinical Laboratory Sc
  • Flynn JL; Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, Pittsburgh, PA 15260, USA. cbarry@niaid.nih.gov joanne@pitt.edu.
Sci Transl Med ; 6(265): 265ra167, 2014 Dec 03.
Article in En | MEDLINE | ID: mdl-25473035
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tomography, X-Ray Computed / Oxazolidinones / Positron-Emission Tomography / Extensively Drug-Resistant Tuberculosis Limits: Animals / Humans Language: En Journal: Sci Transl Med Journal subject: CIENCIA / MEDICINA Year: 2014 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tomography, X-Ray Computed / Oxazolidinones / Positron-Emission Tomography / Extensively Drug-Resistant Tuberculosis Limits: Animals / Humans Language: En Journal: Sci Transl Med Journal subject: CIENCIA / MEDICINA Year: 2014 Document type: Article Affiliation country: