Ahrlund-Richter L, Klein E, Merino F
Immunogenetics. 1982 Jan;15(1):53-62. doi: 10.1007/BF00375502.
H-2 loss variant sublines of a sarcoma (M-AS), induced by methylcholanthrene in an (A x A.SW)F1 mouse, were used to study the role of the MHC products in the recognition of MC-TSTA. The two reciprocal variant sublines (M-A and M-S) were found to express the TSTA of the original tumor as shown by cross-reactions in graft rejection experiments performed in (A x A.SW)F1 mice. In the A/Sn and A.SW mice the presence of the reciprocal parental H-2 antigens on the immunizing cells decreased the response against the tumor antigens. An admixture of lymphocytes derived from hyperimmune mice inhibited the outgrowth of the tumor cells. The growth inhibition was mediated by T cells and was H-2 restricted. Cells derived from hyperimmune immunization but had no effect on the reciprocal variant subline.
用甲基胆蒽在(A×A.SW)F1小鼠中诱导产生的肉瘤(M-AS)的H-2缺失变异亚系,来研究主要组织相容性复合体(MHC)产物在识别甲基胆蒽肿瘤特异性移植抗原(MC-TSTA)中的作用。在(A×A.SW)F1小鼠中进行的移植排斥实验中的交叉反应表明,两个相互对应的变异亚系(M-A和M-S)表达原始肿瘤的TSTA。在A/Sn和A.SW小鼠中,免疫细胞上存在相互对应的亲本H-2抗原会降低对肿瘤抗原的反应。来自超免疫小鼠的淋巴细胞混合物抑制肿瘤细胞的生长。生长抑制由T细胞介导且受H-2限制。来自超免疫免疫的细胞对相互对应的变异亚系没有影响。