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用于免疫单光子发射计算机断层扫描和免疫正电子发射断层扫描分子成像的放射性核素双特异性抗体预靶向:最新进展

Bispecific antibody pretargeting of radionuclides for immuno single-photon emission computed tomography and immuno positron emission tomography molecular imaging: an update.

作者信息

Sharkey Robert M, Karacay Habibe, McBride William J, Rossi Edmund A, Chang Chien-Hsing, Goldenberg David M

机构信息

Garden State Cancer Center, Center for Molecular Medicine and Immunology, Belleville, New Jersey, USA.

出版信息

Clin Cancer Res. 2007 Sep 15;13(18 Pt 2):5577s-5585s. doi: 10.1158/1078-0432.CCR-07-1087.

Abstract

Molecular imaging is intended to localize disease based on distinct molecular/functional characteristics. Much of today's interest in molecular imaging is attributed to the increased acceptance and role of 18F-flurodeoxyglucose (18F-FDG) imaging in a variety of tumors. The clinical acceptance of 18F-FDG has stimulated research for other positron emission tomography (PET) agents with improved specificity to aid in tumor detection and assessment. In this regard, a number of highly specific antibodies have been described for different cancers. Although scintigraphic imaging with antibodies in the past was helpful in patient management, most antibody-based imaging products have not been able to compete successfully with the sensitivity afforded by 18F-FDG-PET, especially when used in combination with computed tomography. Recently, however, significant advances have been made in reengineering antibodies to improve their targeting properties. Herein, we describe progress being made in using a bispecific antibody pretargeting method for immuno-single-photon emission computed tomography and immunoPET applications, as contrasted to directly radiolabeled antibodies. This approach not only significantly enhances tumor/nontumor ratios but also provides high signal intensity in the tumor, making it possible to visualize micrometastases of colonic cancer as small as 0.1 to 0.2 mm in diameter using an anti-carcinoembryonic antigen bispecific antibody, whereas FDG failed to localize these lesions in a nude mouse model. Early detection of micrometastatic non-Hodgkin's lymphoma is also possible using an anti-CD20-based bispecific antibody pretargeting procedure. Thus, this bispecific antibody pretargeting procedure may contribute to tumor detection and could also contribute to the detection of other diseases having distinct antigen targets and suitably specific antibodies.

摘要

分子成像旨在根据独特的分子/功能特征对疾病进行定位。当今对分子成像的诸多兴趣归因于18F-氟脱氧葡萄糖(18F-FDG)成像在多种肿瘤中越来越被接受及其发挥的作用。18F-FDG在临床上的被接受刺激了对其他具有更高特异性的正电子发射断层扫描(PET)剂的研究,以辅助肿瘤检测和评估。在这方面,已经针对不同癌症描述了许多高特异性抗体。尽管过去用抗体进行的闪烁成像有助于患者管理,但大多数基于抗体的成像产品未能成功与18F-FDG-PET所提供的灵敏度竞争,尤其是与计算机断层扫描结合使用时。然而,最近在重新设计抗体以改善其靶向特性方面取得了重大进展。在此,我们描述了与直接放射性标记抗体相比,在免疫单光子发射计算机断层扫描和免疫PET应用中使用双特异性抗体预靶向方法所取得的进展。这种方法不仅显著提高了肿瘤/非肿瘤比率,而且在肿瘤中提供了高信号强度,使得使用抗癌胚抗原双特异性抗体能够在裸鼠模型中可视化直径小至0.1至0.2毫米的结肠癌微转移灶,而FDG未能在该模型中定位这些病变。使用基于抗CD20的双特异性抗体预靶向程序也能够早期检测微转移性非霍奇金淋巴瘤。因此,这种双特异性抗体预靶向程序可能有助于肿瘤检测,也可能有助于检测具有独特抗原靶点和合适特异性抗体的其他疾病。

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