Albinterferon α-2b:: a genetic fusion protein for the treatment of chronic hepatitis C

被引:184
作者
Subramanian, G. Mani
Fiscella, Michele
Lamouse-Smith, Araba
Zeuzem, Stefan
McHutchison, John G.
机构
[1] Human Genome Sci Inc, Rockville, MD 21042 USA
[2] JW Goethe Univ Hosp, D-60590 Frankfurt, Germany
[3] Duke Clin, Res Inst, Durham, NC 27715 USA
关键词
D O I
10.1038/nbt1364
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Treatment regimens based on the use of interferon-alpha (IFN-alpha) remain the cornerstone of therapy for chronic hepatitis C virus infection, which affects nearly 170 million people worldwide. Treatment options include unmodified IFN-alpha given three times weekly or pegylated IFNs given once weekly. The albumin-fusion platform takes advantage of the long half-life of human albumin to provide a new treatment approach that allows the dosing frequency of IFN-alpha to be reduced in individuals with chronic hepatitis C. Albinterferon alpha-2b (alb-IFN), a recombinant polypeptide composed of IFN-alpha 2b genetically fused to human albumin, has an extended half-life and early evidence indicates that it is efficacious and well tolerated. Pharmacodynamic modeling supports treatment with alb-IFN at 2- or 4-week intervals. Phase 3 registration trials are in progress. The albumin-fusion platform is currently being applied to other important bioactive peptides with short half-lives. These fusion proteins, which are at present in different phases of clinical development, might lead to improved therapies across a broad range of diseases.
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页码:1411 / 1419
页数:9
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