Subcutaneously administered interferon-gamma for the treatment of multidrug-resistant pulmonary tuberculosis

Summary Objective We evaluated the clinical and laboratory effects of subcutaneously administered interferon-gamma (IFN-γ) in the treatment of chronic and advanced multidrug-resistant tuberculosis (MDR-TB). Design Eight patients with sputum smear and culture persistently positive MDR-TB were subcutaneously administered 2 million international units of recombinant human IFN-γ three times a week for 24 weeks (72 doses total) between December 2002 and May 2003. Subjects also received a customized drug regimen containing second- and third-line antituberculosis agents based upon drug susceptibility testing and previous treatment history. Results Body weight remained stable or slightly decreased in all subjects during the study period, and none displayed radiographic improvement on serial chest computed tomography scanning. Sputum smears and cultures remained positive for all patients, and there was no increase in the mean time to yield a positive culture (from 16.5 ± 6.4 to 11.8 ± 4.9 days). There was no enhancement of cell-mediated immune responses in terms of production of IFN-γ or IL-10, or of composition of lymphocytes among peripheral blood mononuclear cells. In four patients, therapy was discontinued because of adverse reactions. Conclusion In patients with chronic and advanced MDR-TB, subcutaneous IFN-γ treatment did not result in improvement in clinical, radiologic, microbiologic, or immunologic parameters.