Adenovirus-Mediated InterferonγGene Therapy for Allergic Asthma: Involvement of Interleukin 12 and STAT4 Signaling

Abstract

Allergic asthma is associated with airway inflammation and hyperresponsiveness caused by the dysregulated production of cytokines secreted by allergen-specific helper T type 2 (Th2) cells. Allergic subjects produce relatively low amounts of interferon γ (IFN-γ), a pleiotropic Th1 cytokine that downregulates Th2-associated responses. In this study, we examined the possibility of modulating ovalbumin (OVA)-induced inflammation and airway hyperreactivity (AHR) by recombinant adenovirus-mediated IFN-γ (Ad-IFN-γ) gene transfer. OVA-sensitized mice treated with Ad-IFN-γ exhibit significantly lower levels of Th2 cytokines interleukin 4 (IL-4) and IL-5, OVA-specific serum IgE, lung eosinophilia, and AHR in response to methacholine challenge compared with control mice. The lung sections of the treated mice show less epithelial damage, mucous plugging, and eosinophil infiltration than controls. In contrast, Ad-IFN-γ-treated mice express significantly higher levels of IFN-γ and IL-12 when compared with controls. Moreover, administration of Ad-IFN-γ to mice with established AHR significantly reduced AHR, Th2 cytokines, and lung inflammation. The IFN-γ effects were dependent on IL-12 and STAT4 (signal transducer and activator of transcription 4), as mice treated with antibodies to IL-12 and STAT4 deficient mice show attenuated Ad-IFN-γ responses. Thus, these results demonstrate that mucosal Ad-IFN-γ gene transfer can effectively attenuate established allergen-induced airway inflammation and AHR, predominantly through an IL-12- and STAT4-dependent mechanism.