Pai-Scherf L H, Villa J, Pearson D, Watson T, Liu E, Willingham M C, Pastan I
Laboratory of Molecular Biology, Division of Basic Sciences, National Cancer Institute, NIH, Bethesda, Maryland 20892, USA.
Clin Cancer Res. 1999 Sep;5(9):2311-5.
To exploit overexpression of erbB2 in human cancers, we constructed a single-chain immunotoxin (erb-38) that contains the Fv portion of monoclonal antibody e23 fused to a truncated form of Pseudomonas exotoxin A. In a Phase I study, five breast cancer patients and one esophageal cancer patient received three doses of erb-38 at 1.0 and 2.0 microg/kg. Hepatotoxicity was observed in all patients. Immunohistochemistry showed the presence of erbB2 on hepatocytes explaining the liver toxicity of erb-38. We suggest that targeting of tumors with antibodies to erbB2 armed with radioisotopes or other toxic agents may result in unexpected organ toxicities due to erbB2 on normal cells.
为了利用erbB2在人类癌症中的过表达,我们构建了一种单链免疫毒素(erb - 38),它包含与截短形式的铜绿假单胞菌外毒素A融合的单克隆抗体e23的Fv部分。在一项I期研究中,五名乳腺癌患者和一名食管癌患者接受了三剂剂量为1.0和2.0微克/千克的erb - 38。所有患者均观察到肝毒性。免疫组织化学显示肝细胞上存在erbB2,这解释了erb - 38的肝毒性。我们认为,用携带放射性同位素或其他毒性剂的抗erbB2抗体靶向肿瘤可能会由于正常细胞上的erbB2而导致意外的器官毒性。