Affibody molecules:: potential for in vivo imaging of molecular targets for cancer therapy

被引:110
作者
Tolmachev, Vladimir
Orlova, Anna
Nilsson, Fredrik Y.
Feldwisch, Joachim
Wennborg, Anders
Abrahmsen, Lars
机构
[1] Affibody AB, SE-16102 Bromma, Sweden
[2] Uppsala Univ, Dept Oncol Radiol & Clin Immunol, Unit Biomed Radiat Sci, SE-75185 Uppsala, Sweden
[3] Uppsala Univ, Dept Med Sci Nucl Med, SE-75185 Uppsala, Sweden
关键词
affibody molecules; HER2; molecular imaging; personalized medicine; radionuclide targeting;
D O I
10.1517/14712598.7.4.555
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Targeting radionuclide imaging of tumor-associated antigens may help to select patients who will benefit from a particular biological therapy. Affibody (R) molecules are a novel class of small (similar to 7 kDa) phage display-selected affinity proteins, based on the B-domain scaffold of staphylococcal protein A. A large library (3 x 10(9) variants) has enabled selection of high-affinity (up to 22 pM) binders for a variety of tumor-associated antigens. The small size of Affibody molecules provides rapid tumor localization and fast clearance from nonspecific compartments. Preclinical studies have demonstrated the potential of Affibody molecules for specific and high-contrast radionuclide imaging of HER2 in vivo, and pilot clinical data using indium-111 and gallium-68 labeled anti-HER2 Affibody tracer have confirmed its utility for radionuclide imaging in cancer patients.
引用
收藏
页码:555 / 568
页数:14
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