Comoglio P M, Prat M, Bretti S
Immunology. 1985 Feb;54(2):289-95.
Previous work from this laboratory has shown that preimmunization of syngeneic hosts with Rous sarcoma virus (RSV)-transformed cells elicits a strong immune response against the growth of transplantable RSV sarcomas, mediated by T lymphocytes expressing the surface phenotype of helper cell precursors (Prat, Di Renzo & Comoglio, 1983). This paper shows that anti-tumour immunity may be elicited in tumour-bearing animals by triggering an experimentally pre-amplified T-helper cell population at the site of tumour growth. Mice were treated with cyclophosphamide (which inactivates suppressor T cells) followed by skin sensitization to trinitrochlorobenzene (TNCB) according to a protocol that has been shown to induce an appreciably amplified generation of trinitrophenyl (TNP)-reactive helper T cells (Fujiwara et al., 1984). Five weeks after TNCB painting, mice were transplanted s.c. with a lethal dose of RSV-induced syngeneic sarcoma cells; the injection at the tumour site of TNCB induced the regression of the tumour in mice in which the TNP-helper cell population has been amplified, but not in controls, including those injected with a non-related hapten or sensitized to TNCB without inactivation of suppressors.
该实验室之前的研究表明,用劳氏肉瘤病毒(RSV)转化的细胞对同基因宿主进行预免疫,可引发针对可移植RSV肉瘤生长的强烈免疫反应,该反应由表达辅助细胞前体表型的T淋巴细胞介导(普拉特、迪·伦佐和科莫利奥,1983年)。本文表明,通过在肿瘤生长部位触发实验性预扩增的辅助性T细胞群体,可在荷瘤动物中引发抗肿瘤免疫。按照已证明能诱导明显扩增的三硝基苯基(TNP)反应性辅助性T细胞生成的方案,先用环磷酰胺(可使抑制性T细胞失活)处理小鼠,随后使其对三硝基氯苯(TNCB)产生皮肤致敏(藤原等人,1984年)。在涂抹TNCB五周后,给小鼠皮下移植致死剂量的RSV诱导的同基因肉瘤细胞;在肿瘤部位注射TNCB可使TNP辅助性T细胞群体已扩增的小鼠体内肿瘤消退,但在对照组中则不然,包括那些注射了无关半抗原或在未使抑制性细胞失活的情况下对TNCB致敏的小鼠。