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Sci. STKE, 25 September 2007
Vol. 2007, Issue 405, p. pe53
[DOI: 10.1126/stke.4052007pe53]


Interferon at 50: New Molecules, New Potential, New (and Old) Questions

Jerome A. Langer*

Department of Molecular Genetics, Microbiology, and Immunology, University of Medicine and Dentistry of New Jersey–Robert Wood Johnson Medical School, 675 Hoes Lane West, Piscataway, NJ 08854, USA.

Abstract: Type I interferons (IFNs) are a family of cytokines defined by their antiviral activity but with a broad spectrum of biological activities, including antiproliferative, antitumor, and immunomodulatory effects. Mirroring these activities are diverse therapeutic applications to viral infections, antitumor therapy, and multiple sclerosis. The type I IFNs all signal through a common heterodimeric receptor. The existence of such a large family of cytokines (17 human IFNs) activating a common receptor is unusual. Moreover, the IFNs vary in their relative potency in different assays and are not functionally equivalent. How this functional variation is mediated through a common receptor has not been understood. Reports have now highlighted the interaction of IFNs with the low-affinity receptor subunit IFNAR-1 as a surprising key to their differential activity, particularly regarding antiproliferative and antitumor activities. Two groups have used contrasting approaches to produce variant IFN-{alpha} proteins with novel activity profiles. These advances portend enhanced therapeutic possibilities based on the better understanding of IFN-receptor interactions, while raising interesting mechanistic questions.

*Corresponding author: E-mail, langer{at}

Citation: J. A. Langer, Interferon at 50: New Molecules, New Potential, New (and Old) Questions. Sci. STKE 2007, pe53 (2007).

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