Granstein R D, Parrish J A, McAuliffe D J, Waltenbaugh C, Greene M I
Science. 1984 May 11;224(4649):615-7. doi: 10.1126/science.6231725.
Long-term exposure of C3H mice to ultraviolet radiation resulted in the formation of suppressor T cells that recognize ultraviolet radiation-induced regressor skin cancers as a class before the appearance of overt tumors. Administration of monoclonal antibodies to the product of the I-Jk subregion of the major histocompatibility complex or low doses of cyclophosphamide in vivo inhibited the development or activity of these cells. This activity of the monoclonal antibody was eliminated by adsorption on B10.BR (I-Jk) but not B10.D2 (I-Jd) splenocytes. These findings provide evidence that elements expressing the I-J determinant are important in regulating the host response prior to the overt development of ultraviolet radiation-induced skin cancers and suggest novel therapeutic approaches to malignancies or other diseases involving suppressor T cells in their pathogenesis.
将C3H小鼠长期暴露于紫外线辐射下,会导致在明显肿瘤出现之前,形成一类能识别紫外线辐射诱导的退行性皮肤癌的抑制性T细胞。在体内给予针对主要组织相容性复合体I-Jk亚区产物的单克隆抗体或低剂量环磷酰胺,可抑制这些细胞的发育或活性。这种单克隆抗体的活性可被B10.BR(I-Jk)脾细胞吸附消除,但不能被B10.D2(I-Jd)脾细胞吸附消除。这些发现提供了证据,表明表达I-J决定簇的成分在紫外线辐射诱导的皮肤癌明显发展之前调节宿主反应中起重要作用,并提示了针对恶性肿瘤或其他在发病机制中涉及抑制性T细胞的疾病的新治疗方法。