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使用单链Fv和γ干扰素改进肿瘤放射免疫检测:放射免疫导向手术和γ扫描的潜在临床应用

Improved tumor radioimmunodetection using a single-chain Fv and gamma-interferon: potential clinical applications for radioimmunoguided surgery and gamma scanning.

作者信息

Nieroda C A, Milenic D E, Carrasquillo J A, Scholm J, Greiner J W

机构信息

Laboratory of Tumor Immunology and Biology, National Cancer Institute, NIH, Bethesda, Maryland 20892, USA.

出版信息

Cancer Res. 1995 Jul 1;55(13):2858-65.

PMID:7796413
Abstract

Previous studies have shown that (a) single-chain antibody binding proteins, or sFvs, localize experimental tumor xenografts (D.E. Milenic et al, Cancer Res., 51: 6363-6371, 1991) and (b) the administration of gamma-interferon (IFN-gamma) increases the expression of a high molecular weight glycoprotein, tumor-associated glycoprotein 72 (TAG-72), which improves mAb-based tumor targeting as well as radioimmunotherapy (J. W. Greiner et al., Cancer Res., 53: 600-608, 1993). The present experimental study was designed to determine whether exploiting those two observations in combination could augment tumor detection. Initial results revealed significant localization of a single-chain antibody binding protein of CC49 (i.e., CC49 sFv), a second generation anti-TAG-72 mAb, to human colon tumor xenografts (HT-29), which express low constitutive TAG-72 levels. IFN-gamma treatment of mice bearing HT-29 tumors significantly increased TAG-72 levels in the tumor xenografts. Increased TAG-72 expression was accompanied by a 2-4-fold augmentation of CC49 sFv localized to the HT-29 tumors, measured by direct quantitation of 125I-labeled CC49 sFv tumor deposition as well as tumor:normal tissue ratios. Enhanced CC49 sFv tumor localization improved HT-29 tumor visualization by external scintigraphy as well as when using a hand-held gamma-detecting probe to discriminate between normal (i.e., heart, hind leg) and tumor tissue. The gamma-detecting probe was the same as that used intraoperatively with 125I-labeled CC49 IgG to identify occult tumors in patients. The present experimental findings indicate that the efficiency by which 125I-labeled CC49 sFv localizes tumor in vivo can be enhanced with IFN-gamma. Results of the present study suggest that (a) the incorporation of an IFN-gamma treatment schema prior to radioimmunscintigraphy may increase the signal from the tumor site(s), thus providing a better discrimination between tumor and background, and (b) combining 125I-labeled CC49 sFv with IFN-gamma will not only reduce the time interval between antibody injection and surgery, but will also increase the efficiency of tumor localization using the intraoperative gamma-detecting probe.

摘要

先前的研究表明

(a)单链抗体结合蛋白,即单链抗体片段(sFv),可使实验性肿瘤异种移植瘤定位(D.E. 米莱尼克等人,《癌症研究》,51: 6363 - 6371, 1991年);(b)给予γ干扰素(IFN - γ)可增加一种高分子量糖蛋白——肿瘤相关糖蛋白72(TAG - 72)的表达,这可改善基于单克隆抗体的肿瘤靶向性以及放射免疫疗法(J.W. 格雷纳等人,《癌症研究》,53: 600 - 608, 1993年)。本实验研究旨在确定联合利用这两项观察结果是否能增强肿瘤检测。初步结果显示,第二代抗TAG - 72单克隆抗体CC49的单链抗体结合蛋白(即CC49 sFv)可显著定位于人结肠肿瘤异种移植瘤(HT - 29),该肿瘤表达的TAG - 72基础水平较低。对荷HT - 29肿瘤的小鼠进行IFN - γ治疗可显著提高肿瘤异种移植瘤中的TAG - 72水平。通过直接定量125I标记的CC49 sFv在肿瘤中的沉积以及肿瘤与正常组织的比值来测量,TAG - 72表达的增加伴随着定位于HT - 29肿瘤的CC49 sFv增加2至4倍。增强的CC49 sFv肿瘤定位通过外部闪烁扫描以及使用手持式γ探测仪区分正常组织(即心脏、后腿)和肿瘤组织,改善了HT - 29肿瘤的可视化。γ探测仪与术中用于识别患者隐匿肿瘤的125I标记的CC49 IgG所使用的仪器相同。本实验结果表明,IFN - γ可提高125I标记的CC49 sFv在体内使肿瘤定位的效率。本研究结果提示:(a)在放射免疫闪烁扫描之前加入IFN - γ治疗方案可能会增加肿瘤部位的信号,从而更好地区分肿瘤与背景;(b)将125I标记的CC49 sFv与IFN - γ联合使用不仅会缩短抗体注射与手术之间的时间间隔,还会提高术中使用γ探测仪进行肿瘤定位的效率。

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