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 |
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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. 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.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 9635566</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>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. 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M</creatorcontrib><creatorcontrib>DINARELLO, C. A</creatorcontrib><creatorcontrib>HERBERMAN, R. B</creatorcontrib><creatorcontrib>WILLIAMS, B. R. G</creatorcontrib><creatorcontrib>BORDEN, E. C</creatorcontrib><creatorcontrib>BORDENS, R</creatorcontrib><creatorcontrib>WALTER, M. R</creatorcontrib><creatorcontrib>NAGABHUSHAN, T. L</creatorcontrib><creatorcontrib>TROTTA, P. P</creatorcontrib><creatorcontrib>PESTKA, S</creatorcontrib><title>Biological properties of recombinant α-interferons : 40th anniversary of the discovery of interferons</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><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.</description><subject>Antibiotics. Antiinfectious agents. Antiparasitic agents</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Agents - chemistry</subject><subject>Antineoplastic Agents - metabolism</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Antiviral agents</subject><subject>Antiviral Agents - chemistry</subject><subject>Antiviral Agents - metabolism</subject><subject>Antiviral Agents - pharmacology</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Binding, Competitive</subject><subject>Biological and medical sciences</subject><subject>Cytokines - antagonists & inhibitors</subject><subject>Dinoprostone - physiology</subject><subject>Forecasting</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Interferon Type I - chemistry</subject><subject>Interferon Type I - metabolism</subject><subject>Interferon Type I - pharmacology</subject><subject>Interferon Type I - therapeutic use</subject><subject>Medical sciences</subject><subject>Neoplasms - drug therapy</subject><subject>Pharmacology. Drug treatments</subject><subject>Protein Conformation</subject><subject>Receptor, Interferon alpha-beta</subject><subject>Receptors, Interferon - drug effects</subject><subject>Receptors, Interferon - metabolism</subject><subject>Recombinant Proteins</subject><subject>Signal Transduction</subject><subject>Treatment Outcome</subject><subject>Virus Diseases - drug therapy</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM9KxDAQxoMo67r6CEIO4q2QNP9ab7r4Dxa86Llkk6kbaZOadAUfyxfxmcxqEW-ehpn5zfB93x6aU8GqQnEu9tGcEFIVgqvyEB2l9JJbQYmYoVktmRBSzlF75UIXnp3RHR5iGCCODhIOLY5gQr92XvsRf34Uzo8QW4jBJ3yBORk3WHvv3iAmHd93B-MGsHXJhDz7Hvw5OUYHre4SnEx1gZ5urh-Xd8Xq4fZ-ebkqhlLKsbCgKqqkpZwRQ2omjZTEVkxrRo2lWnAQRmWmyp5YyY0iklmwIBlldQVsgc5__mYvr1tIY9NnRdB12kPYpkbVteAZ_RekqiQ5oCqDpxO4XfdgmyG6PhtupgTz_mza65RDbKP2xqVfbKeSM8m-AAIUey8</recordid><startdate>19980615</startdate><enddate>19980615</enddate><creator>PFEFFER, L. 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Antiparasitic agents</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Agents - chemistry</topic><topic>Antineoplastic Agents - metabolism</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Antiviral agents</topic><topic>Antiviral Agents - chemistry</topic><topic>Antiviral Agents - metabolism</topic><topic>Antiviral Agents - pharmacology</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Binding, Competitive</topic><topic>Biological and medical sciences</topic><topic>Cytokines - antagonists & inhibitors</topic><topic>Dinoprostone - physiology</topic><topic>Forecasting</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Interferon Type I - chemistry</topic><topic>Interferon Type I - metabolism</topic><topic>Interferon Type I - pharmacology</topic><topic>Interferon Type I - therapeutic use</topic><topic>Medical sciences</topic><topic>Neoplasms - drug therapy</topic><topic>Pharmacology. Drug treatments</topic><topic>Protein Conformation</topic><topic>Receptor, Interferon alpha-beta</topic><topic>Receptors, Interferon - drug effects</topic><topic>Receptors, Interferon - metabolism</topic><topic>Recombinant Proteins</topic><topic>Signal Transduction</topic><topic>Treatment Outcome</topic><topic>Virus Diseases - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PFEFFER, L. M</creatorcontrib><creatorcontrib>DINARELLO, C. A</creatorcontrib><creatorcontrib>HERBERMAN, R. B</creatorcontrib><creatorcontrib>WILLIAMS, B. R. G</creatorcontrib><creatorcontrib>BORDEN, E. C</creatorcontrib><creatorcontrib>BORDENS, R</creatorcontrib><creatorcontrib>WALTER, M. R</creatorcontrib><creatorcontrib>NAGABHUSHAN, T. L</creatorcontrib><creatorcontrib>TROTTA, P. 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P</au><au>PESTKA, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biological properties of recombinant α-interferons : 40th anniversary of the discovery of interferons</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>1998-06-15</date><risdate>1998</risdate><volume>58</volume><issue>12</issue><spage>2489</spage><epage>2499</epage><pages>2489-2499</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>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.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>9635566</pmid><tpages>11</tpages></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals |
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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