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

Author:

Nguyen Khuong B.1,Watford Wendy T.2,Salomon Rachelle1,Hofmann Sigrun R.2,Pien Gary C.1,Morinobu Akio2,Gadina Massimo2,O'Shea John J.2,Biron Christine A.1

Affiliation:

1. Department of Molecular Microbiology and Immunology, Division of Biology and Medicine, Brown University, Providence, RI 02912, USA.

2. Molecular Immunology and Inflammation Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD 20892, USA.

Abstract

Interferons (IFNs) are essential for host defense. Although the antiviral effects of the type 1 IFNs IFN-α and IFN-β (IFN-α/β) have been established, their immunoregulatory functions, especially their ability to regulate IFN-γ production, are poorly understood. Here we show that IFN-α/β activate STAT4 directly (STAT, signal transducers and activators of transcription) and that this is required for IFN-γ production during viral infections of mice, in concert with T cell receptor–derived signals. In contrast, STAT1 appears to negatively regulate IFN-α/β induction of IFN-γ. 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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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