Finlay-Jones J J, Hart P H
Department of Microbiology and Infectious Diseases, School of Medicine, and Flinders Cancer Centre, Flinders University of South Australia, Adelaide, Australia.
Australas J Dermatol. 1997 Jun;38 Suppl 1:S7-12. doi: 10.1111/j.1440-0960.1997.tb01001.x.
Ultraviolet (UV) radiation, particularly in the UVB region (280-320 nm), is immunosuppressive. This modulation of the immune response to antigens following UV irradiation allows the outgrowth of UV-induced skin cancers. Because UV irradiation penetrates only a few millimetres into the skin, yet can induce not only a local but also a systemic immunosuppression, the transducing mechanisms must be superficially located. Three mechanisms have been put forward, one which identifies epidermal urocanic acid as the photoreceptor, one that identifies DNA, and one that identifies cell membrane lipid peroxidation as initiating immunomodulation. While a number of mechanisms may operate (or cooperate), and do so differentially for local vs systemic suppression, considerable evidence supports urocanic acid as a key photoreceptor for immunosuppression. This review examines the immunomodulatory effects of urocanic acid, as well as its role in facilitating the outgrowth of UV-induced skin cancer.
紫外线(UV)辐射,尤其是UVB区域(280 - 320纳米)的辐射,具有免疫抑制作用。紫外线照射后对抗原免疫反应的这种调节使得紫外线诱导的皮肤癌得以生长。由于紫外线照射仅能穿透皮肤几毫米,但不仅能诱导局部免疫抑制,还能诱导全身免疫抑制,所以转导机制必定位于皮肤表层。已经提出了三种机制,一种认为表皮尿刊酸是光感受器,一种认为是DNA,还有一种认为细胞膜脂质过氧化是引发免疫调节的因素。虽然可能有多种机制在起作用(或协同作用),并且局部抑制和全身抑制的作用方式有所不同,但大量证据支持尿刊酸是免疫抑制的关键光感受器。这篇综述探讨了尿刊酸的免疫调节作用,以及它在促进紫外线诱导的皮肤癌生长中的作用。