Enhancement of the innate and cellular immune response in patients with genital warts treated with topical imiquimod cream 5
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- 作者：Arany ; Istvan ; Tyring ; Stephen K. ; Stanley ; Margaret A. ; Tomai ; Mark A. ; Miller ; Richard L. ; et. al.
- 关键词：Aldara&trade ; Cytokine ; Condylomata acuminata ; Human papilloma virus ; Imiquimod ; Interferon ; 2&prime ; 5&prime ; -AS ; 2&prime ; 5&prime ; oligoadenylate synthetase ; CMI ; cell mediated immunity ; CTL ; cytotoxic T-cells ; EOT ; end of treatment ; HPV ; human papillo
- 刊名：Antiviral Research
- 出版年：1999
- 出版时间：August, 1999
- 年：1999
- 卷：43
- 期：1
- 页码：55-63
- 全文大小：262 K
文摘
The mechanism of action of imiquimod 5 % cream applied topically to patients with genital warts was evaluated in a double-blind, placebo-controlled study. Imiquimod (16 patients) or placebo (three patients) was applied three times per week for up to 16 weeks. All imiquimod-treated patients had a ≥75 % reduction in total wart area while only one of three placebo-treated patients had a similar reduction. Wart biopsies were taken at prestudy, week 6, and end of treatment. Polymerase chain reaction (PCR) for human papillomavirus (HPV) DNA and reverse transcriptase (RT)-PCR for messenger (m)RNAs were used to identify cytokines, cellular markers, viral gene products, and cell cycle markers in these biopsies. Treatment with imiquimod, an immune response modifier, stimulated significant increases in mRNA for interferon (IFN)-α, IFN-γ and 2′,5′ oligoadenylate synthetase (2′,5′-AS) as well as a tendency towards increases in tumor necrosis factor (TNF)-α and interleukin-12 p40. Significant increases in mRNA for CD4 and a trend toward increases in CD8 were also observed in imiquimod-treated patients, suggesting activation of a cell mediated immune response. Imiquimod administration was also associated with a significant decrease in viral load as measured by HPV DNA and L1 mRNA. The effects on HPV markers were accompanied by an apparent decrease in mRNA expression for markers of cell proliferation and an increase in mRNA for markers of keratinocyte differentiation and tumor suppressors.