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抗表皮生长因子受体单克隆抗体:生物学研究及潜在临床应用

Anti-EGF receptor monoclonal antibodies: biological studies and potential clinical applications.

作者信息

Mendelsohn J

机构信息

Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY

出版信息

Trans Am Clin Climatol Assoc. 1989;100:31-8.

Abstract

We have produced two monoclonal antibodies (mAbs), 528 IgG2a and 225 IgG1, which bind to the human EGF receptor with an affinity comparable to EGF, compete with EGF for binding to the receptor, and prevent EGF-induced activation of receptor tyrosine kinase. The mAbs inhibit the proliferation of a number of human tumor cells bearing high numbers of EGF receptors in culture and in nude mouse xenographs. A431 xenographs bearing high numbers of EGF receptors can be imaged with 111In-labeled mAb. Phase I trials were initiated in patients with advanced squamous cell carcinoma of the lung, which consistently expresses high numbers of EGF receptors. 111In-labeled 225 IgG1 was given by single intravenous infusion. Preliminary results show no toxicity from doses up to 120 mg. Tumor visualization was seen to be dose-related. However, as with other imaging studies with indium-labeled antibodies, significant liver and bowel isotope uptake was observed. Further dose escalation is ongoing to assess the relationship between dose and tumor uptake.

摘要

我们制备了两种单克隆抗体(mAb),528 IgG2a和225 IgG1,它们与人类表皮生长因子(EGF)受体结合的亲和力与EGF相当,能与EGF竞争结合受体,并阻止EGF诱导的受体酪氨酸激酶激活。这些单克隆抗体在体外培养和裸鼠异种移植模型中抑制了许多表达大量EGF受体的人类肿瘤细胞的增殖。携带大量EGF受体的A431异种移植瘤可用111铟标记的单克隆抗体进行成像。针对肺鳞状细胞癌晚期且持续高表达大量EGF受体的患者开展了I期试验。通过单次静脉输注给予111铟标记的225 IgG1。初步结果显示,剂量高达120 mg时无毒性。肿瘤显影与剂量相关。然而,与其他铟标记抗体的成像研究一样,观察到肝脏和肠道有明显的同位素摄取。正在进一步提高剂量以评估剂量与肿瘤摄取之间的关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d160/2376448/f77144d891c2/tacca00088-0094-a.jpg

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