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Evaluation of a novel type of imaging probe based on a recombinant bivalent mini-antibody construct for detection of CD44v6-expressing squamous cell carcinoma

机译:基于重组双价微型抗体构建体的新型成像探针用于检测表达CD44v6的鳞状细胞癌的评估

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摘要

We have developed the CD44v6-targeting human bivalent antibody fragment AbD19384, an engineered recombinant human bivalent Fab antibody formed via dimerization of dHLX (synthetic double helix loop helix motif) domains, for potential use in antibody-based molecular imaging of squamous cell carcinoma in the head and neck region. This is a unique construct that has, to the best of our knowledge, never been assessed for molecular imaging in vivo before. The objective of the present study was to evaluate for the first time the in vitro and in vivo binding properties of radio-iodinated AbD19384, and to assess its utility as a targeting agent for molecular imaging of CD44v6-expressing tumors. Antigen specificity and binding properties were assessed in vitro. In vivo specificity and biodistribution of 125I-AbD19384 were next evaluated in tumor-bearing mice using a dual-tumor setup. Finally, AbD19384 was labeled with 124I, and its imaging properties were assessed by small animal PET/CT in tumor bearing mice, and compared with 2-deoxy-2-[18F]fluoro-D-glucose (18F-FDG). In vitro studies demonstrated CD44v6-specific binding with slow off-rate for AbD19384. A favorable biodistribution profile was seen in vivo, with tumor-specific uptake. Small animal PET/CT images of 124I-AbD19384 supported the results through clearly visible high CD44v6-expressing tumors and faintly visible low expressing tumors, with superior imaging properties compared to 18F-FDG. Tumor-to-blood ratios increased with time for the conjugate (assessed up to 72 h p.i.), although 48 h p.i. proved best for imaging. Biodistribution and small-animal PET studies demonstrated that the recombinant Fab-dHLX construct AbD19384 is a promising tracer for imaging of CD44v6 antigen expression in vivo, with the future aim to be used for individualized diagnosis and early detection of squamous cell carcinomas in the head and neck region. Furthermore, this proof-of-concept research established the feasibility of using recombinant Fab-dHLX constructs for in vivo imaging of tumor biomarkers.
机译:我们已经开发了靶向CD44v6的人二价抗体片段AbD19384,该工程重组人二价Fab抗体是通过dHLX(合成双螺旋环螺旋基序)域的二聚化形成的,可用于基于抗体的鳞状细胞癌分子成像中头和颈部区域。据我们所知,这是一个独特的构建体,之前从未进行过体内分子成像评估。本研究的目的是首次评估放射性碘化AbD19384的体外和体内结合特性,并评估其作为表达CD44v6的肿瘤分子成像的靶向剂的效用。体外评估抗原特异性和结合特性。接下来使用双肿瘤设置在荷瘤小鼠中评估125 I-AbD19384的体内特异性和生物分布。最后,将AbD19384标记为124I,并通过小型动物PET / CT在荷瘤小鼠中评估其成像特性,并与2-deoxy-2- [18F] fluoro-D-葡萄糖(18F-FDG)进行比较。体外研究表明,CD44v6特异性结合对于AbD19384具有缓慢的失活速率。在体内发现了有利的生物分布特征,并具有肿瘤特异性摄取。 124I-AbD19384的小动物PET / CT图像通过清晰可见的高CD44v6表达肿瘤和微弱可见的低表达肿瘤支持了该结果,与18F-FDG相比,具有优越的成像性能。结合物的肿瘤血比随时间增加(评估为每小时72小时),尽管每小时48小时。被证明最适合成像。生物分布和小动物PET研究表明,重组Fab-dHLX构建体AbD19384是用于体内CD44v6抗原表达成像的有前途的示踪剂,其未来目标是用于个体诊断和早期发现头部和头部鳞状细胞癌颈部。此外,这项概念验证研究确立了将重组Fab-dHLX构建体用于肿瘤生物标记物体内成像的可行性。

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