Chen L, Mizuno M T, Singhal M C, Hu S L, Galloway D A, Hellström I, Hellström K E
Bristol-Myers Squibb Pharmaceutical Research Institute, Seattle, WA 98121.
J Immunol. 1992 Apr 15;148(8):2617-21.
Human papillomavirus (HPV) type 16 has been implicated in the etiology of cervical carcinomas, but it is unknown whether HPV-specific immunity can function in controlling the growth of HPV-associated carcinomas. We previously demonstrated that CD8+ T lymphocytes can inhibit the in vivo outgrowth of murine tumor cells transfected with the HPV-16 E7 gene and have now established a murine model to study the CTL responses to the E6 oncoprotein of HPV-16. Immunization of C3H/HeN mice with syngeneic fibroblasts expressing a transfected HPV-16 E6 gene induced regression of transplanted tumors expressing this gene. Populations of CTL isolated from the spleens of mice whose E6+ tumors had regressed were shown to specifically lyse E6+ target cells. The cytolytic activity was mediated by CD8+ CTL in a MHC restricted pattern. These data and our previous findings with transfected tumor cells expressing the E7 gene, support the conclusion that tumor cells associated with HPV-16 can be inhibited by CTL specific for molecules encoded by the HPV-16 E6 and E7 genes.
人乳头瘤病毒16型(HPV-16)与宫颈癌的病因有关,但HPV特异性免疫是否能控制HPV相关癌的生长尚不清楚。我们之前证明,CD8 + T淋巴细胞可抑制转染了HPV-16 E7基因的小鼠肿瘤细胞在体内的生长,并且现在已经建立了一个小鼠模型来研究CTL对HPV-16 E6癌蛋白的反应。用表达转染的HPV-16 E6基因的同基因成纤维细胞免疫C3H/HeN小鼠,可诱导表达该基因的移植肿瘤消退。从E6 +肿瘤已消退的小鼠脾脏中分离出的CTL群体可特异性裂解E6 +靶细胞。细胞溶解活性由CD8 + CTL以MHC限制模式介导。这些数据以及我们之前对表达E7基因的转染肿瘤细胞的研究结果支持以下结论:与HPV-16相关的肿瘤细胞可被针对HPV-16 E6和E7基因编码分子的CTL抑制。