Critical Role for STAT4 Activation by Type 1 Interferons in the Interferon-γ Response to Viral Infection

Khuong B. Nguyen(Brown University), Wendy T. Watford(National Institutes of Health), Rachelle Salomon(Brown University), Sigrun R. Hofmann(National Institutes of Health), Gary C. Pien(Brown University), Akio Morinobu(National Institutes of Health), Massimo Gadina(National Institutes of Health), John J. O’Shea(National Institutes of Health), Christine A. Biron(Brown University)
Science
September 19, 2002
Cited by 490

Abstract

Interferons (IFNs) are essential for host defense. Although the antiviral effects of the type 1 IFNs IFN-alpha and IFN-beta (IFN-alpha/beta) have been established, their immunoregulatory functions, especially their ability to regulate IFN-gamma production, are poorly understood. Here we show that IFN-alpha/beta activate STAT4 directly (STAT, signal transducers and activators of transcription) and that this is required for IFN-gamma production during viral infections of mice, in concert with T cell receptor-derived signals. In contrast, STAT1 appears to negatively regulate IFN-alpha/beta induction of IFN-gamma. Thus, type 1 IFNs, in addition to interleukin-12, provide pathways for innate regulation of adaptive immunity, and their immunoregulatory functions are controlled by modulating the activity of individual STATs.


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