Rosenblum M G, Murray J L, Cheung L, Rifkin R, Salmon S, Bartholomew R
Department of Clinical Immunology and Biological Therapy, M.D. Anderson Cancer Center, Houston, TX 77030.
Mol Biother. 1991 Mar;3(1):6-13.
Murine monoclonal antibody ZME-018 recognizes a 240 Kda glycoprotein present on the surface of most human melanoma cells and on over 80% of human biopsy specimens tested. Gelonin is a ribosome-inactivating plant toxin similar in nature and rivaling the activity of ricin A chain. ZME-018 was coupled to purified gelonin using the reagents SPDP and 2-iminothiolane. The ZME-gelonin conjugate was purified by S-300 Sephacryl and Blue Sepharose chromatography, removing unreacted gelonin and antibody, respectively. PAGE analysis showed that ZME was coupled to 1, 2, or 3 gelonin molecules. The ZME-gelonin conjugate was 10(6)-fold more active than gelonin itself in inhibiting the growth of log-phase human melanoma cells in culture. The immunoconjugate was not cytotoxic to antigen negative T-24 (human bladder carcinoma) cells. Treatment of melanoma cells with recombinant IFN-alpha or TNF substantially augmented the cytotoxicity of the immunoconjugate while treatment with IFN-gamma had a minor effect. Using the human tumor colony assay of melanoma cells obtained from fresh biopsy specimens, greater than 90% growth suppression was observed in 2 of 4 samples tested at a concentration of 250 ng/ml. In addition, 25% growth suppression was observed with a third sample tested, and no growth suppression was observed in 1 sample. Thus, clonogenic melanoma cells are sensitive in vitro to the cytotoxic activity of this immunotoxin at concentrations which we presume are pharmacologically relevant.
鼠单克隆抗体ZME - 018识别一种240千道尔顿的糖蛋白,该糖蛋白存在于大多数人黑色素瘤细胞表面以及超过80%的检测人活检标本中。Gelonin是一种核糖体失活植物毒素,性质与蓖麻毒素A链相似且活性相当。使用试剂SPDP和2 - 亚氨基硫杂环戊烷将ZME - 018与纯化的Gelonin偶联。通过S - 300 Sephacryl和蓝色琼脂糖凝胶层析纯化ZME - Gelonin偶联物,分别去除未反应的Gelonin和抗体。PAGE分析表明ZME与1、2或3个Gelonin分子偶联。在抑制培养中对数期人黑色素瘤细胞生长方面,ZME - Gelonin偶联物比Gelonin本身活性高10^6倍。该免疫偶联物对抗原阴性的T - 24(人膀胱癌)细胞无细胞毒性。用重组IFN - α或TNF处理黑色素瘤细胞可显著增强免疫偶联物的细胞毒性,而用IFN - γ处理效果较小。使用从新鲜活检标本获得的人黑色素瘤细胞的人肿瘤集落测定法,在浓度为250 ng/ml时,4个测试样本中有2个观察到大于90%的生长抑制。此外,第三个测试样本观察到25%的生长抑制,1个样本未观察到生长抑制。因此,克隆性黑色素瘤细胞在体外对这种免疫毒素的细胞毒性敏感,我们推测该浓度具有药理学相关性。