Tamura K, Ishida N
Gan To Kagaku Ryoho. 1984 Jul;11(7):1369-78.
Tumor necrosis factor (TNF) can be induced in BALB/c mice bearing syngeneic tumor RL male 1 lymphoma or Meth A fibrosarcoma, by initial injection of either Corynebacterium parvum or BCG, in combination with a second injection of endotoxin (LPS) almost 10 days later. Either treatment resulted in hemorrhagic necrosis and complete regression of tumors in mice. The term, "endogenous induction of TNF therapy" was proposed for this trial. Although the TNF of tumor-bearing mice was identical to that of normal mice in molecular weight (about 40,000 daltons) and isoelectric point (4.4), and differed from IFN, the in vivo effect of endogenous TNF was much more remarkable than in mice receiving passive TNF administration. The mice bearing RL male 1 lymphoma cured after endogenous induction of TNF, rejected rechallenge of the same tumor cells but not Meth-A tumor cells. Splenocytes obtained from these cured mice were also found to be inhibitory in Winn's neutralization assay. The data indicate that tumor-specific immunity can be induced in mice receiving endogenous induction of TNF.
肿瘤坏死因子(TNF)可在携带同基因肿瘤RL雄性1淋巴瘤或Meth A纤维肉瘤的BALB/c小鼠中诱导产生,方法是先注射短小棒状杆菌或卡介苗,然后在大约10天后再注射内毒素(LPS)。两种处理方法均可导致小鼠肿瘤出现出血性坏死并完全消退。该试验提出了“内源性TNF诱导疗法”这一术语。尽管荷瘤小鼠的TNF在分子量(约40,000道尔顿)和等电点(4.4)方面与正常小鼠的TNF相同,且与干扰素不同,但内源性TNF的体内效应比接受被动TNF给药的小鼠更为显著。经内源性TNF诱导治愈的携带RL雄性1淋巴瘤的小鼠,能够排斥相同肿瘤细胞的再次攻击,但不能排斥Meth-A肿瘤细胞。在温氏中和试验中还发现,从这些治愈小鼠获得的脾细胞具有抑制作用。数据表明,接受内源性TNF诱导的小鼠可诱导产生肿瘤特异性免疫。