一种由ZME-018抗体和植物毒素凝胶蛋白组成的特异性强效免疫毒素。

Molecular biotherapy Pub Date : 1991-03-01
M G Rosenblum, J L Murray, L Cheung, R Rifkin, S Salmon, R Bartholomew
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引用次数: 0

摘要

小鼠单克隆抗体ZME-018可识别大多数人黑色素瘤细胞表面和80%以上的人活检标本表面存在的240 Kda糖蛋白。蓖麻毒素是一种与蓖麻毒素a链活性相似的核糖体失活植物毒素。ZME-018用SPDP试剂和2-亚氨基硫烷试剂偶联纯化明胶。ZME-gelonin偶联物采用S-300 Sephacryl层析和Blue Sepharose层析纯化,分别去除未反应的gelonin和抗体。PAGE分析显示ZME与1、2或3个gelonin分子偶联。ZME-gelonin偶联物在抑制培养的对数期人类黑色素瘤细胞生长方面的活性比gelonin本身高10(6)倍。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治疗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治疗效果较小。使用从新鲜活检标本中获得的黑色素瘤细胞的人类肿瘤集落测定,在250 ng/ml浓度下,4个样本中有2个样本的生长抑制大于90%。此外,在第三个样品中观察到25%的生长抑制,在1个样品中没有观察到生长抑制。因此,克隆源性黑色素瘤细胞在体外对这种免疫毒素的细胞毒性活性敏感,我们认为这种免疫毒素的浓度与药理学有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A specific and potent immunotoxin composed of antibody ZME-018 and the plant toxin gelonin.

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.

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