Mavligit G M, Hersh E M
Med Pediatr Oncol. 1978;5(1):115-26. doi: 10.1002/mpo.2950050118.
Mononuclear cell-mediated cytotoxicity (MCMC) against cultured tumor target cells was studied sequentially in melanoma and breast cancer patients before and during BGC administration. MCMC showed temporary fluctuations. In patients with locally advanced melanoma and carcinoma of the breast after tumor load reduction, the administration of BCG may increase the MCMC. This did not always correlate with a favorable clinical course. Potentiating serum factors appeared in 50% of these patients during BCG therapy, while blocking factors were rare. Neither correlated with prognosis. In patients with disseminated melanoma receiving chemoimmunotherapy, increases in MCMC may be related to clinical course. Blocking serum factors frequently developed in this group of patients and potentiating factors were rare. Neither correlated with the clinical course. Significant MCMC among normal donors and the apparent lack of specificity suggest a common nonspecific (? natural) cellular reactivity against cultured tumor target cells.
在给予卡介苗(BCG)之前及期间,对黑色素瘤和乳腺癌患者针对培养肿瘤靶细胞的单核细胞介导的细胞毒性(MCMC)进行了连续研究。MCMC表现出暂时波动。在局部晚期黑色素瘤和乳腺癌患者肿瘤负荷降低后,给予BCG可能会增加MCMC。这并不总是与良好的临床病程相关。在50%的此类患者接受BCG治疗期间出现了增强血清因子,而阻断因子很少见。两者均与预后无关。在接受化学免疫治疗的播散性黑色素瘤患者中,MCMC的增加可能与临床病程有关。在这组患者中经常出现阻断血清因子,而增强因子很少见。两者均与临床病程无关。正常供体中显著的MCMC以及明显缺乏特异性表明针对培养肿瘤靶细胞存在一种常见的非特异性(?天然)细胞反应性。