Taetle R, Dos Santos B, Ohsugi Y, Koishihara Y, Yamada Y, Messner H, Dalton W
Arizona Cancer Center, Tucson 85724.
J Natl Cancer Inst. 1994 Mar 16;86(6):450-5. doi: 10.1093/jnci/86.6.450.
Although passive serotherapy for cancer with monoclonal antibodies is an attractive concept, it has unfortunately had limited efficacy in clinical trials. An alternative approach to passive serotherapy is targeting cell surface growth factor receptors with monoclonal antibodies. With some limitations, anti-growth factor receptor antibodies can limit cell growth by blocking stimulatory or trophic growth factor receptors and by marshaling in vivo antitumor immune responses.
The purpose of our study was to determine the extent to which anti-interleukin-6 (IL-6) and anti-transferrin (Tf) receptor antibodies, when used individually or combined, could limit myeloma cell growth.
The four myeloma cell lines studied varied in IL-6 responses from factor independence (myeloma cell lines 8226 and U266) to strict factor dependence (OCI-My4 myeloma cells and human acute myelogenous leukemia [AML] cell line UCSD/AML1). IL-6 RNA was detected using reverse transcriptase-polymerase chain reaction. IL-6 protein was detected in U266 supernatant by growth stimulation of UCSD/AML1 cells and by enzyme-linked immunosorbent assay. For cell growth assays, cell lines were plated with various concentrations of IL-6 and anti-receptor antibodies and [3H]thymidine uptake determined after 3 days. Cells were grown in varying concentrations of IgG1 monoclonal anti-Tf receptor antibodies E2.3 and A27.15 or antibodies PM1, AUK 146-15, AUK 64-7, or AUK 12-20 to the human IL-6 receptor-alpha protein. Tf and IL-6 receptors were detected by immunofluorescence staining.
Using short-term proliferation assays, anti-Tf receptors and anti-IL-6 antibodies caused dose-dependent growth inhibition of varying degrees, and, in one of three cell lines, a combination of anti-Tf and anti-IL-6 antibodies showed supra-additive growth inhibition. IL-6-independent cells were inhibited by anti-Tf receptor antibodies, while IL-6-dependent cells were resistant to these antibodies but sensitive to anti-IL-6 receptor. Factor-dependent myeloma cells exposed to either anti-Tf or anti-IL-6 receptor antibodies for 48 hours lost colony-forming capability. A combination of anti-Tf and anti-IL-6 antibodies increased elimination of colony-forming cells at 24 hours.
Anti-receptor antibodies have distinct patterns of myeloma cell growth inhibition and inhibit in vitro growth of factor-dependent myeloma cells. Combinations of anti-growth factor receptor antibodies also increase toxicity for IL-6-dependent myeloma colony-forming units.
尽管用单克隆抗体进行癌症的被动血清疗法是一个很有吸引力的概念,但遗憾的是,它在临床试验中的疗效有限。被动血清疗法的一种替代方法是用单克隆抗体靶向细胞表面生长因子受体。尽管存在一些局限性,但抗生长因子受体抗体可通过阻断刺激性或营养性生长因子受体以及调动体内抗肿瘤免疫反应来限制细胞生长。
我们研究的目的是确定抗白细胞介素-6(IL-6)和抗转铁蛋白(Tf)受体抗体单独使用或联合使用时能在多大程度上限制骨髓瘤细胞的生长。
所研究的四种骨髓瘤细胞系对IL-6的反应各不相同,从因子非依赖性(骨髓瘤细胞系8226和U266)到严格的因子依赖性(OCI-My4骨髓瘤细胞和人急性髓性白血病[AML]细胞系UCSD/AML1)。使用逆转录聚合酶链反应检测IL-6 RNA。通过UCSD/AML1细胞的生长刺激和酶联免疫吸附测定法检测U266上清液中的IL-6蛋白。对于细胞生长测定,将细胞系接种于含有不同浓度IL-6和抗受体抗体的培养基中,3天后测定[3H]胸腺嘧啶核苷摄取量。细胞在不同浓度的IgG1单克隆抗Tf受体抗体E2.3和A27.15或针对人IL-6受体α蛋白的抗体PM1、AUK 146-15、AUK 64-7或AUK 12-20中培养。通过免疫荧光染色检测Tf和IL-6受体。
使用短期增殖试验,抗Tf受体和抗IL-6抗体引起不同程度的剂量依赖性生长抑制,并且在三个细胞系中的一个中,抗Tf和抗IL-6抗体的组合显示出超加成生长抑制。IL-6非依赖性细胞被抗Tf受体抗体抑制,而IL-6依赖性细胞对这些抗体有抗性,但对抗IL-6受体敏感。暴露于抗Tf或抗IL-6受体抗体48小时的因子依赖性骨髓瘤细胞丧失集落形成能力。抗Tf和抗IL-6抗体的组合在24小时时增加了集落形成细胞的清除率。
抗受体抗体具有不同的骨髓瘤细胞生长抑制模式,并抑制因子依赖性骨髓瘤细胞的体外生长。抗生长因子受体抗体的组合也增加了对IL-6依赖性骨髓瘤集落形成单位的毒性。