Siegall C B
Molecular Immunology Department, Bristol-Myers Squibb, Pharmaceutical Research Institute, Seattle, WA 98121, USA.
Semin Cancer Biol. 1995 Oct;6(5):289-95. doi: 10.1006/scbi.1995.0037.
Monoclonal antibody BR96 recognizes a Le(y)-related carbohydrate antigen expressed on a wide range of carcinomas. Immunotoxins composed of BR96 and a binding defective form of Pseudomonas exotoxin A were constructed both as chemical conjugates and as fusion proteins. While both forms of BR96 immunotoxin were equally cytotoxic to human carcinoma cell lines in vitro, the fusion protein form, BR96 sFv-PE40, was > 10-fold more active in vivo as an antitumor agent. BR96 sFv-PE40 was used to target established human tumor xenografts in both mice and in rats. The rat which displays the Le(y) antigen on the same normal tissues as humans appears to be an appropriate model for the preclinical evaluation of this immunotoxin. Complete regressions of lung, breast and bladder carcinomas were obtained in these models upon administration of well-tolerated doses of BR96 sFv-PE40. The clinical limitations of BR96 sFv-PE40, as well as other immunotoxins, depend on the management and/or prevention of neutralizing anti-immunotoxin antibodies and the onset of toxicities, specifically vascular leak syndrome.
单克隆抗体BR96可识别多种癌组织上表达的一种与Le(y)相关的碳水化合物抗原。由BR96和一种结合缺陷型绿脓杆菌外毒素A构建的免疫毒素,既可以制成化学偶联物,也可以制成融合蛋白。虽然两种形式的BR96免疫毒素在体外对人癌细胞系具有同等的细胞毒性,但融合蛋白形式的BR96 sFv-PE40在体内作为抗肿瘤药物的活性要高10倍以上。BR96 sFv-PE40被用于靶向小鼠和大鼠体内已建立的人肿瘤异种移植物。在与人类相同的正常组织上表达Le(y)抗原的大鼠,似乎是对这种免疫毒素进行临床前评估的合适模型。在这些模型中,给予耐受性良好剂量的BR96 sFv-PE40后,肺癌、乳腺癌和膀胱癌实现了完全消退。BR96 sFv-PE40以及其他免疫毒素的临床局限性,取决于对中和抗免疫毒素抗体的管理和/或预防以及毒性的发生,特别是血管渗漏综合征。