Biological properties of recombinant α-interferons : 40th anniversary of the discovery of interferons

IFNs were first described as potent antiviral agents 40 years ago, and recombinant IFN-alpha2a and IFN-alpha2b were approved for the treatment of hairy cell leukemia just 11 years ago. Today, alpha-IFNs are approved worldwide for the treatment of a variety of malignancies and virologic diseases. Alt...

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Veröffentlicht in:Cancer research (Chicago, Ill.) Ill.), 1998-06, Vol.58 (12), p.2489-2499
Hauptverfasser: PFEFFER, L. M, DINARELLO, C. A, HERBERMAN, R. B, WILLIAMS, B. R. G, BORDEN, E. C, BORDENS, R, WALTER, M. R, NAGABHUSHAN, T. L, TROTTA, P. P, PESTKA, S
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container_end_page 2499
container_issue 12
container_start_page 2489
container_title Cancer research (Chicago, Ill.)
container_volume 58
creator PFEFFER, L. M
DINARELLO, C. A
HERBERMAN, R. B
WILLIAMS, B. R. G
BORDEN, E. C
BORDENS, R
WALTER, M. R
NAGABHUSHAN, T. L
TROTTA, P. P
PESTKA, S
description IFNs were first described as potent antiviral agents 40 years ago, and recombinant IFN-alpha2a and IFN-alpha2b were approved for the treatment of hairy cell leukemia just 11 years ago. Today, alpha-IFNs are approved worldwide for the treatment of a variety of malignancies and virologic diseases. Although the exact mechanism of action of IFN-alpha in the treatment of such diseases is not fully understood, many advances have been made in the characterization of the physicochemical and diverse biological properties of this highly pleiotropic cytokine. Here we review recent developments in our understanding of the antiviral and immunoregulatory properties of IFN-alpha, the nature of the multisubunit IFN-alpha receptor, and the molecular mechanisms of signal transduction. Where available, we have included comparative data on recombinant alpha-IFNs derived from both naturally occurring and nonnaturally occurring synthetic genes. We also review clinical data and data on the side effects and antigenicity of different sources of recombinant alpha-IFNs in humans. These latter topics are of clinical interest, because they may potentially affect the efficacy of these various products. Hopefully, what is already known about IFN will prompt further exploration into the mechanism(s) of action of IFN-alpha and thus deliver new applications for this prototypic cytokine, whose full therapeutic potential is yet to be realized.
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M ; DINARELLO, C. A ; HERBERMAN, R. B ; WILLIAMS, B. R. G ; BORDEN, E. C ; BORDENS, R ; WALTER, M. R ; NAGABHUSHAN, T. L ; TROTTA, P. P ; PESTKA, S</creator><creatorcontrib>PFEFFER, L. M ; DINARELLO, C. A ; HERBERMAN, R. B ; WILLIAMS, B. R. G ; BORDEN, E. C ; BORDENS, R ; WALTER, M. R ; NAGABHUSHAN, T. L ; TROTTA, P. P ; PESTKA, S</creatorcontrib><description>IFNs were first described as potent antiviral agents 40 years ago, and recombinant IFN-alpha2a and IFN-alpha2b were approved for the treatment of hairy cell leukemia just 11 years ago. Today, alpha-IFNs are approved worldwide for the treatment of a variety of malignancies and virologic diseases. Although the exact mechanism of action of IFN-alpha in the treatment of such diseases is not fully understood, many advances have been made in the characterization of the physicochemical and diverse biological properties of this highly pleiotropic cytokine. Here we review recent developments in our understanding of the antiviral and immunoregulatory properties of IFN-alpha, the nature of the multisubunit IFN-alpha receptor, and the molecular mechanisms of signal transduction. Where available, we have included comparative data on recombinant alpha-IFNs derived from both naturally occurring and nonnaturally occurring synthetic genes. We also review clinical data and data on the side effects and antigenicity of different sources of recombinant alpha-IFNs in humans. These latter topics are of clinical interest, because they may potentially affect the efficacy of these various products. 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Hopefully, what is already known about IFN will prompt further exploration into the mechanism(s) of action of IFN-alpha and thus deliver new applications for this prototypic cytokine, whose full therapeutic potential is yet to be realized.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>9635566</pmid><tpages>11</tpages></addata></record>
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subjects Antibiotics. Antiinfectious agents. Antiparasitic agents
Antineoplastic agents
Antineoplastic Agents - chemistry
Antineoplastic Agents - metabolism
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Antiviral agents
Antiviral Agents - chemistry
Antiviral Agents - metabolism
Antiviral Agents - pharmacology
Antiviral Agents - therapeutic use
Binding, Competitive
Biological and medical sciences
Cytokines - antagonists & inhibitors
Dinoprostone - physiology
Forecasting
Humans
Immunotherapy
Interferon Type I - chemistry
Interferon Type I - metabolism
Interferon Type I - pharmacology
Interferon Type I - therapeutic use
Medical sciences
Neoplasms - drug therapy
Pharmacology. Drug treatments
Protein Conformation
Receptor, Interferon alpha-beta
Receptors, Interferon - drug effects
Receptors, Interferon - metabolism
Recombinant Proteins
Signal Transduction
Treatment Outcome
Virus Diseases - drug therapy
title Biological properties of recombinant α-interferons : 40th anniversary of the discovery of interferons
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