Imbertson L M, Beaurline J M, Couture A M, Gibson S J, Smith R M, Miller R L, Reiter M J, Wagner T L, Tomai M A
3M Pharmaceuticals, Department of Pharmacology, St. Paul, Minnesota 55144, USA.
J Invest Dermatol. 1998 May;110(5):734-9. doi: 10.1046/j.1523-1747.1998.00174.x.
ALDARA (imiquimod cream 5%) recently became available for the treatment of genital and perianal warts; however, the topical mechanism of action of imiquimod is not fully understood. Imiquimod, and its analogs R-842, S-27609, and S-28463, are potent anti-viral and anti-tumor agents in animal models. Much of the biologic activity of these compounds can be attributed to the induction of cytokines, including interferon-alpha, tumor necrosis factor-alpha, interleukins-1, -6, -8, and others. This study was performed to characterize the response of mice and rats to topical application of imiquimod and S-28463 and also to evaluate these agents in cultures of murine and human skin cells. Topical administration of imiquimod or S-28463 to the flanks of hairless mice and rats leads to increases in local concentrations of interferon and tumor necrosis factor in the skin. The concentrations of interferon and tumor necrosis factor were higher at the site of drug application than in skin from the contralateral flank or skin from untreated animals. Interferon-alpha mRNA levels were also elevated in the skin of mice after topical application of either imiquimod or S-28463. In vitro, both imiquimod and S-28463 induced increases in interferon and tumor necrosis factor in cultures of cells isolated from hairless mouse skin. Imiquimod also increased interleukin-8 concentrations in human keratinocyte and fibroblast cultures, whereas S-28463 induced increases in tumor necrosis factor in fibroblast cultures. These results demonstrate that imiquimod and S-28463 stimulate production of cytokines in the skin after topical application, which may play a major role in its activity in genital wart patients.
艾达乐(咪喹莫特乳膏5%)最近被批准用于治疗生殖器和肛周疣;然而,咪喹莫特的局部作用机制尚未完全明确。咪喹莫特及其类似物R-842、S-27609和S-28463在动物模型中是有效的抗病毒和抗肿瘤药物。这些化合物的许多生物学活性可归因于细胞因子的诱导,包括α-干扰素、肿瘤坏死因子-α、白细胞介素-1、-6、-8等。本研究旨在描述小鼠和大鼠对局部应用咪喹莫特和S-28463的反应,并在小鼠和人类皮肤细胞培养物中评估这些药物。对无毛小鼠和大鼠的胁腹局部应用咪喹莫特或S-28463会导致皮肤中干扰素和肿瘤坏死因子的局部浓度增加。药物应用部位的干扰素和肿瘤坏死因子浓度高于对侧胁腹皮肤或未处理动物的皮肤。局部应用咪喹莫特或S-28463后,小鼠皮肤中的α-干扰素mRNA水平也会升高。在体外,咪喹莫特和S-28463均可诱导从无毛小鼠皮肤分离的细胞培养物中干扰素和肿瘤坏死因子增加。咪喹莫特还可增加人角质形成细胞和成纤维细胞培养物中白细胞介素-8的浓度,而S-28463可诱导成纤维细胞培养物中肿瘤坏死因子增加。这些结果表明,局部应用后,咪喹莫特和S-28463可刺激皮肤中细胞因子的产生,这可能在其对生殖器疣患者的活性中起主要作用。