Kripke M L
Immunol Rev. 1984 Aug;80:87-102. doi: 10.1111/j.1600-065x.1984.tb00496.x.
Immunological unresponsiveness can be initiated by exposure of mice to UV radiation, followed by the introduction of certain antigens. These antigens include epicutaneously applied chemicals that induce contact hypersensitivity (CHS), and antigens that occur on skin cancers induced by UV radiation. Mice exposed repeatedly to high doses of UV radiation during UV carcinogenesis develop immunological unresponsiveness to UV radiation-induced skin cancers, which are highly antigenic. This unresponsiveness is associated with the appearance of suppressor T lymphocytes that are specific for tumors induced by UV radiation, even though these tumors express individually specific transplantation rejection antigens. Thus, the occurrence of suppressor cells with specificity for a set of non-cross-reacting tumors suggests that a common, UV-associated regulatory antigen or determinant may be present on UV-induced skin cancers. Suppression of CHS in mice by UV radiation can be induced by two different procedures. One involves applying the sensitizer directly on skin exposed to low doses of UV-B radiation and is thought to result from a direct effect of UV radiation on cutaneous Langerhans cells. The second involves application of the sensitizer to the unirradiated skin of mice or guinea pigs exposed several days earlier to a higher dose of UV-B radiation. The mechanism of the latter phenomenon is not well understood, but there is evidence that it results from an alteration of antigen presentation by splenic macrophages. Both forms of suppression are associated with the appearance of antigen-specific suppressor lymphocytes in the animals' spleens, which prevent the induction of CHS upon transfer to a normal recipient. Either or both of these pathways could be responsible for the formation of the suppressor cells involved in UV carcinogenesis. Recent studies suggest that UV radiation may also affect immunological responsiveness in humans as well as in animals. However, the extent of such alterations and the mechanisms by which they occur are still unknown.
免疫无反应性可通过将小鼠暴露于紫外线辐射,随后引入某些抗原引发。这些抗原包括经皮应用可诱导接触性超敏反应(CHS)的化学物质,以及紫外线辐射诱导的皮肤癌上出现的抗原。在紫外线致癌过程中反复暴露于高剂量紫外线辐射的小鼠,会对紫外线辐射诱导的皮肤癌产生免疫无反应性,而这些皮肤癌具有高度抗原性。这种无反应性与针对紫外线辐射诱导肿瘤的抑制性T淋巴细胞的出现有关,尽管这些肿瘤各自表达特异性移植排斥抗原。因此,对一组非交叉反应性肿瘤具有特异性的抑制细胞的出现表明,紫外线诱导的皮肤癌上可能存在一种共同的、与紫外线相关的调节抗原或决定簇。紫外线辐射对小鼠CHS的抑制可通过两种不同程序诱导。一种是将致敏剂直接应用于暴露于低剂量UV - B辐射的皮肤上,被认为是紫外线辐射对皮肤朗格汉斯细胞的直接作用导致的。另一种是将致敏剂应用于几天前暴露于较高剂量UV - B辐射的小鼠或豚鼠的未照射皮肤上。后一种现象的机制尚不完全清楚,但有证据表明这是脾脏巨噬细胞对抗原呈递的改变所致。两种抑制形式都与动物脾脏中抗原特异性抑制淋巴细胞的出现有关,这些抑制淋巴细胞转移到正常受体后可阻止CHS的诱导。这些途径中的一种或两种都可能是参与紫外线致癌作用的抑制细胞形成的原因。最近的研究表明,紫外线辐射可能也会影响人类以及动物的免疫反应性。然而,这种改变的程度及其发生机制仍然未知。