Taş Sinan, Avci Oktay
Yasemin Sokak No. 6, Narlidere, Manavkuyu Mahallesi 244 Sokak, 5-1/2 Bornova, Izmir, Turkey.
Dermatology. 2004;209(2):126-31. doi: 10.1159/000079596.
We have earlier found a highly efficient induction of the differentiation of epidermal lineage skin tumors by cyclopamine, a steroidal alkaloid inhibitor of the hedgehog/smoothened signaling, under conditions in which cyclopamine exerted no adverse effect on skin.
We aimed to develop a mechanism-based treatment for psoriasis with cyclopamine.
We subjected psoriatic skin lesions to cyclopamine under conditions similar to those we used for skin tumors and evaluated the responses of lesions clinically and by histopathological/immunohistochemical analyses.
All treated lesions in different patients having plaque and guttate forms of psoriasis regressed rapidly. Differentiation of the epidermal cells of lesional skin and disappearances of infiltrating inflammatory cells were evident within a day. Lesions were cleared commonly on days 3-4. Former treatment sites followed up for more than 24 months now show a lack of adverse effects in the long term.
An effective treatment for psoriasis is described, consistent with intervention in a proximal/key pathogenic event.
我们之前发现,环杷明(一种刺猬信号通路/ smoothened信号甾体生物碱抑制剂)在对皮肤无不良影响的条件下,能高效诱导表皮谱系皮肤肿瘤的分化。
我们旨在研发一种基于机制的环杷明治疗银屑病的方法。
我们在与皮肤肿瘤实验相似的条件下,对银屑病皮损应用环杷明,并通过临床评估以及组织病理学/免疫组织化学分析来评价皮损的反应。
不同患者的斑块状和点滴状银屑病的所有治疗皮损均迅速消退。皮损皮肤的表皮细胞分化以及浸润性炎症细胞消失在一天内就很明显。皮损通常在第3 - 4天清除。之前治疗部位随访超过24个月,目前显示长期无不良反应。
描述了一种有效的银屑病治疗方法,这与干预近端/关键致病事件一致。