IFN-α 2B Enhances Th1 Cytokine Responses in Bladder Cancer Patients Receiving Mycobacterium bovis Bacillus Calmette-Guérin Immunotherapy

Abstract

Combination therapy with intravesical bacillus Calmette-Guérin (BCG) plus IFN-α for superficial bladder cancer has been demonstrated to be more effective than either single agent alone in animal studies and of suggested greater efficacy in clinical studies. However, the mechanism by which IFN-α enhances BCG-mediated antitumor activity is poorly understood. Using PBMCs from bladder cancer patients, IFN-α was found to substantially enhance the efficacy of BCG to induce IFN-γ production. Among 34 patients tested, 80% showed >4-fold increase. This effect of IFN-α was observed in both initial and memory responses to BCG. In addition, IFN-α up-regulated BCG-induced IL-12 and TNF-α and down-regulated BCG-induced IL-10. Neutralizing endogenous IL-10 or adding exogenous IL-12 provided further synergy for IFN-γ production. In clinical practice, intravesical IFN-α 2B (50 million units (MU)/dose) was observed to accelerate urinary IFN-γ production to low-dose BCG (one-tenth or one-third of a full dose) in patients treated with combination therapy compared with BCG alone. These results suggest that IFN-α is a potent BCG enhancer that polarizes the BCG-induced immune response toward the cellular immune pathway by promoting Th1 cytokine expression and reducing Th2 cytokine expression. This study provides an immunological basis for future rational use of IFN-α in conjunction with intravesical BCG for bladder cancer immunotherapy.