Norval Mary, McLoone Pauline, Lesiak Aleksandra, Narbutt Joanna
Biomedical Sciences, University of Edinburgh Medical School, Edinburgh, UK.
Photochem Photobiol. 2008 Jan-Feb;84(1):19-28. doi: 10.1111/j.1751-1097.2007.00239.x.
A single or a limited number of UVR exposures is recognized to suppress cell-mediated immunity in human subjects. The complex pathway leading from the absorption of photons by chromophores in the skin to the generation of T regulatory cells has been, at least partially, elucidated. However, the effect of repeated UV exposures on immune responses and associated mediators is not well studied, particularly to assess whether they lead, first, to the development of photoprotection so that these immune changes are reduced or no longer occur, and, secondly, to the development of photoprotection against the normal downregulation of immunity induced by a high UV dose. For almost all the parameters evaluated in this review--epidermal DNA damage/erythema, urocanic acid, Langerhans and dendritic cells, natural killer cells, macrophages, mast cells, contact and delayed hypersensitivity responses--none, aside from epidermal DNA damage/erythema and macrophage phagocytic activity, show convincing evidence of photoadaptation or, where appropriate, photoprotection. It is concluded that repeatedly irradiating individuals with UVR is likely to continue to result in downregulation of immunity.
单次或有限次数的紫外线(UVR)照射被认为会抑制人体的细胞介导免疫。从皮肤中的发色团吸收光子到产生调节性T细胞的复杂途径至少已部分阐明。然而,反复紫外线照射对免疫反应及相关介质的影响尚未得到充分研究,尤其是要评估它们是否首先导致光保护的产生,从而使这些免疫变化减少或不再发生,其次是否导致针对高剂量紫外线诱导的正常免疫下调的光保护的产生。对于本综述中评估的几乎所有参数——表皮DNA损伤/红斑、尿刊酸、朗格汉斯细胞和树突状细胞、自然杀伤细胞、巨噬细胞、肥大细胞、接触性和迟发型超敏反应——除了表皮DNA损伤/红斑和巨噬细胞吞噬活性外,没有其他参数显示出令人信服的光适应或(如适用)光保护的证据。得出的结论是,反复用紫外线照射个体可能会继续导致免疫下调。