Pryor K, Goddard J, Goldstein D, Stricker P, Russell P, Golovsky D, Penny R
Centre for Immunology, St Vincent's Hospital, Sydney, NSW, Australia.
Br J Cancer. 1995 Apr;71(4):801-7. doi: 10.1038/bjc.1995.155.
A cytotoxicity assay was used to study the action of bacillus Calmette-Guerin (BCG) and cytokines on four human bladder cancer cell lines. Monocytes and lymphocytes from peripheral blood were incubated with or without BCG or cytokines for 24 h, after which [3H]thymidine-labelled target cells were added and the 72 h percentage specific release determined. BCG had a direct cytotoxic effect against tumour cells and significantly enhanced monocyte/macrophage and enhanced lymphocyte cytotoxicity against one cell line (UCRU-BL-17). Supernatants (SNs) from BCG-activated monocytes/macrophages and lymphocytes increased the percentage specific release of [3H]thymidine from UCRU-BL-17 cells. Interferon alpha (IFN-alpha) and interleukin 2 (IL-2) were cytotoxic towards UCRU-BL-17. No synergy occurred between BCG and cytokines at the concentrations tested. The results suggest that BCG is superior to IFN-alpha, interferon gamma (IFN-gamma) and IL-2 in enhancing cell-mediated cytotoxicity.
采用细胞毒性试验研究卡介苗(BCG)和细胞因子对四种人膀胱癌细胞系的作用。外周血中的单核细胞和淋巴细胞在有或无BCG或细胞因子的情况下孵育24小时,之后加入[3H]胸腺嘧啶核苷标记的靶细胞,并测定72小时的特异性释放百分比。BCG对肿瘤细胞具有直接细胞毒性作用,并显著增强单核细胞/巨噬细胞以及增强淋巴细胞对一种细胞系(UCRU-BL-17)的细胞毒性。BCG激活的单核细胞/巨噬细胞和淋巴细胞的上清液增加了UCRU-BL-17细胞中[3H]胸腺嘧啶核苷的特异性释放百分比。α干扰素(IFN-α)和白细胞介素2(IL-2)对UCRU-BL-17具有细胞毒性。在测试浓度下,BCG与细胞因子之间未发生协同作用。结果表明,在增强细胞介导的细胞毒性方面,BCG优于IFN-α、γ干扰素(IFN-γ)和IL-2。