Meyer T, Nindl I, Schmook T, Ulrich C, Sterry W, Stockfleth E
Institute of Immunology, Clinical Pathology and Molecular Medicine, Lademannbogen 61, 22339 Hamburg, Germany.
Br J Dermatol. 2003 Nov;149 Suppl 66:9-14. doi: 10.1046/j.0366-077x.2003.05632.x.
Toll-like receptor (TLR)-7 agonists represent a new group of immune response modifiers, which include imiquimod and resiquimod (R-848). Topically applied imiquimod is used for the treatment of both external and perianal genital warts, and benign and malignant epithelial lesions. Based on the induction of interferons and other cytokines in vitro and in vivo, regression of epithelial lesions probably depends on induction of both innate and cellular immune responses. As clinical remission is not always associated with inflammation, other mechanisms may also be involved. Using two different assays for detection of apoptosis (TUNEL test and gel analysis of DNA fragmentation), we observed induction of apoptosis by imiquimod in human epithelial cell lines (HeLa S3) and keratinocytes (HaCaT, A431 cells), as well as in mouse fibroblasts (McCoy cells). These findings suggest that the mode of action of imiquimod to eliminate virus-infected, dysplastic or neoplastic epithelial cells may also include the induction of apoptotic processes.
Toll样受体(TLR)-7激动剂是一类新型免疫反应调节剂,包括咪喹莫特和瑞喹莫特(R-848)。局部应用的咪喹莫特可用于治疗外部和肛周生殖器疣以及良性和恶性上皮病变。基于体外和体内干扰素及其他细胞因子的诱导作用,上皮病变的消退可能依赖于固有免疫和细胞免疫反应的诱导。由于临床缓解并不总是与炎症相关,可能还涉及其他机制。我们使用两种不同的凋亡检测方法(TUNEL检测和DNA片段化凝胶分析),观察到咪喹莫特可诱导人上皮细胞系(HeLa S3)、角质形成细胞(HaCaT、A431细胞)以及小鼠成纤维细胞(McCoy细胞)发生凋亡。这些发现表明,咪喹莫特消除病毒感染、发育异常或肿瘤性上皮细胞的作用方式可能还包括诱导凋亡过程。