Journal List > Tuberc Respir Dis > v.57(3) > 1000682

Kim, Shim, Lee, Oh, Lim, Lee, Koh, Kim, Kim, and Kim: The Adjuvant Effect of Subcutaneous Interferon-gamma in the Treatment of Refractory Multidrug-resistant Pulmonary Tuberculosis

Abstract

Background

Interferon-gamma (IFN-γ) is a critical cytokine in the defense against a Mycobacterium tuberculosis infection. Even though IFN-γ has occasionally been used in the treatment of refractory multidrug-resistant tuberculosis (MDR-TB) with some promising results, there is still some controversy regarding the therapeutic efficacy of IFN-γ. This study was performed to examine the effect of subcutaneous IFN-γ in the treatment of MDR-TB patients.

Methods

Six patients with refractory MDR-TB were enrolled in this study. Two million IU of IFN-γ was administered subcutaneously three times a week with the concomitant administration of antituberculous drugs for at least for 28 weeks. During the IFN-γ therapy, the sputum smear and culture, radiological and clinical evaluations were performed every 4 weeks throughout the study period.

Results

The mean age of the 6 patients was 37 years (ranges, 15-61 years). The drug susceptibility test to standard antituberculous drugs revealed resistance to an average of 6.8 (±1.2) agents including isoniazid and rifampicin. An average of 10.8 (±1.3) antituberculous drugs were prescribed before IFN-γ therapy. The culture became negative in 2 patients (33%) after initiating IFN-γ therapy; one at 8 weeks, and the other at 24 weeks. Finally, after stopping the IFN-γ therapy after 28 weeks, the culture became positive again in the two patients who were culture-negative. The other 4 patients who failed in the culture conversion are still on antituberculous treatment except for one who died of tuberculosis.

Conclusion

Even though 28 weeks of subcutaneous IFN-γ therapy in combination with antituberculous drugs was successful in inducing the culture-negative conversion in some patients with refractory MDR-TB, the culture became positive again after stopping the IFN-γ therapy. This suggests that subcutaneous IFN-γ therapy may have suppressive effect on tuberculosis only during the IFN-γ therapy period in some patients. Further studies will be needed to determine the optimum dose, the administration route, the duration of therapy, and the predicting factors of the response to adjuvant IFN-γ therapy.

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