A novel drug screening assay for papillomavirus specific antiviral activity

被引:13
|
作者
Clark, PR [1 ]
Roberts, ML [1 ]
Cowsert, LM [1 ]
机构
[1] ISIS Pharmaceut, Dept Infect Dis, Carlsbad, CA 92008 USA
关键词
human papilloma virus type 11; DNA replication assay; antiviral drug screening assay;
D O I
10.1016/S0166-3542(97)00066-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Discovery and development of human papillomavirus (HPV) specific antiviral agents have been hampered by the lack of an in vitro assay permissive to HPV replication. An experimental assay system for monitoring HPV-11 DNA replication has been optimized for use as a papillomavirus antiviral drug screening tool. Cloned HPV DNA was introduced into SCC-4 cells by electroporation and viral DNA replication monitored by Southern blot. Kinetic studies demonstrated an increased HPV genome copy number with time. Viral DNA replicated as episomal, unit length genome and remained episomal after multiple passages. These data suggested the basis for an in vitro replication assay for evaluating the antiviral activity of potential chemotherapeutic agents directly on HPV. This model was used to investigate antiviral activities of current anti-HPV therapies such as 5-fluorouracil (5-FU) and alpha-interferon (alpha-IFN) and potential therapies such as sodium butyrate, 5-bromo-2O-deoxyuridine (BrdU) and antisense oligonucleotides. HPV-11 replication is significantly inhibited by BrdU and sodium butyrate; however 5-FU and a-IFN did not give consistent dose response results. Finally, ISIS 2105, a 20-mer phosphorothioate antisense oligonucleotide, which targets HPV-11 E2, gene product, showed potent antiviral activity in this assay with an IC50 of approximate to 70 nM. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:97 / 106
页数:10
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