The type I IFNs (IFN-α and IFN-β) were first characterized as cytokines capable of inducing an antiviral state in sensitive target cells (1). They were originally classified as leukocyte IFN and fibroblast IFN, respectively, to designate their distinct presumptive cellular origins. This designation has been replaced by a more precise nomenclature, based on molecular characterization after the isolation, cloning, and sequencing of the IFN multigene family. The originally detected IFN-α activity is encoded by a multigene family of closely related and clustered genes, while IFN-β is encoded by a single, somewhat more distantly related gene. It has also become clear that type I IFNs can be synthesized by many, if not all, nucleated cells, just as virtually all nucleated cells have the capacity to respond to secreted IFN to induce an antiviral state. This ability of most cells to secrete and respond to...
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18 February 2002
Commentary|
February 19 2002
Whence Interferon? Variety in the Production of Interferon in Response to Viral Infection
David E. Levy
David E. Levy
Molecular Oncology and Immunology Program, Department of Pathology and Kaplan Comprehensive Cancer Center, New York University School of Medicine, New York, NY 10016
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David E. Levy
Molecular Oncology and Immunology Program, Department of Pathology and Kaplan Comprehensive Cancer Center, New York University School of Medicine, New York, NY 10016
Address correspondence to David Levy, Molecular Oncology and Immunology Program, Dept. of Pathology and Kaplan Comprehensive Cancer Center, New York University School of Medicine, 550 First Ave., New York, NY 10016. Phone: 212-263-8192; Fax: 212-263-8211; E-mail: [email protected]
Received:
January 16 2002
Accepted:
January 21 2002
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2002
J Exp Med (2002) 195 (4): F15–F18.
Article history
Received:
January 16 2002
Accepted:
January 21 2002
Citation
David E. Levy; Whence Interferon? Variety in the Production of Interferon in Response to Viral Infection . J Exp Med 18 February 2002; 195 (4): F15–F18. doi: https://doi.org/10.1084/jem.20020075
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