Fujita M, Miyachi Y, Horio T, Imamura S
Department of Dermatology, Faculty of Medicine, Kyoto University, Japan.
J Dermatol Sci. 1990 Jul;1(4):289-96. doi: 10.1016/0923-1811(90)90122-t.
Biopsy specimens of chronic lesions and ultraviolet-induced lesions from actinic reticuloid patients were examined by immunoperoxidase techniques and compared with those of allergic contact dermatitis skin, one of the delayed-type hypersensitivity conditions. Each lesion of actinic reticuloid showed a clear predominance of suppressor/cytotoxic T cells to helper/inducer T cells and an increase of Langerhans cells in the epidermis and the dermis. These findings are generally similar to those in the late phase (on day 7 and 11) but not in the early phase (on day 2) of allergic contact dermatitis and suggest that delayed-type hypersensitivity might be involved in some parts of the pathogenesis of actinic reticuloid. CD36+DR+ epidermal cells were also observed in ultraviolet-induced lesions from actinic reticuloid patients, suggesting a possible role in the modulation of the mechanism.
采用免疫过氧化物酶技术对光化性类网状细胞增生症患者的慢性病变和紫外线诱导病变的活检标本进行检查,并与迟发型超敏反应性疾病之一的过敏性接触性皮炎皮肤的活检标本进行比较。光化性类网状细胞增生症的每个病变均显示抑制性/细胞毒性T细胞相对于辅助性/诱导性T细胞明显占优势,且表皮和真皮中的朗格汉斯细胞增多。这些发现总体上与过敏性接触性皮炎晚期(第7天和第11天)相似,但与早期(第2天)不同,提示迟发型超敏反应可能参与了光化性类网状细胞增生症发病机制的某些环节。在光化性类网状细胞增生症患者的紫外线诱导病变中也观察到CD36+DR+表皮细胞,提示其可能在调节机制中发挥作用。