Development of an 18F-labeled anti-human CD8 VHH for same-day immunoPET imaging

被引:11
|
作者
Sriraman, Shravan Kumar [1 ]
Davies, Christopher W. [2 ]
Gill, Herman [1 ]
Kiefer, James R. [3 ]
Yin, Jianping [3 ]
Ogasawara, Annie [1 ]
Urrutia, Alejandra [4 ]
Javinal, Vincent [5 ]
Lin, Zhonghua [2 ]
Seshasayee, Dhaya [2 ]
Abraham, Ryan [6 ]
Haas, Phil [6 ]
Koth, Christopher [3 ]
Marik, Jan [1 ]
Koerber, James T. [2 ]
Williams, Simon Peter [1 ]
机构
[1] Genentech Inc, Dept Biomed Imaging, 1 DNA Way, San Francisco, CA 94080 USA
[2] Genentech Inc, Dept Antibody Engn, 1 DNA Way, San Francisco, CA 94080 USA
[3] Genentech Inc, Dept Struct Biol, 1 DNA Way, San Francisco, CA 94080 USA
[4] Genentech Inc, Dept Canc Immunol, 1 DNA Way, San Francisco, CA 94080 USA
[5] Genentech Inc, Dept In Vivo Pharmacol, 1 DNA Way, San Francisco, CA 94080 USA
[6] Genentech Inc, Dept Prot Chem, 1 DNA Way, San Francisco, CA 94080 USA
基金
美国国家卫生研究院;
关键词
CD8; ImmunoPET; VHH; F-18-fluoride; EXPRESSION; RECOGNITION; NANOBODIES; BLOCKADE; SEQUENCE;
D O I
10.1007/s00259-022-05998-0
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose Cancer immunotherapies (CITs) have revolutionized the treatment of certain cancers, but many patients fail to respond or relapse from current therapies, prompting the need for new CIT agents. CD8(+) T cells play a central role in the activity of many CITs, and thus, the rapid imaging of CD8(+) cells could provide a critical biomarker for new CIT agents. However, existing Zr-89-labeled CD8 PET imaging reagents exhibit a long circulatory half-life and high radiation burden that limit potential applications such as same-day and longitudinal imaging. Methods To this end, we discovered and developed a 13-kDa single-domain antibody (VHH5v2) against human CD8 to enable high-quality, same-day imaging with a reduced radiation burden. To enable sensitive and rapid imaging, we employed a site-specific conjugation strategy to introduce an F-18 radiolabel to the VHH. Results The anti-CD8 VHH, VHH5v2, demonstrated binding to a membrane distal epitope of human CD8 with a binding affinity (K-D) of 500 pM. Subsequent imaging experiments in several xenografts that express varying levels of CD8 demonstrated rapid tumor uptake and fast clearance from the blood. High-quality images were obtained within 1 h post-injection and could quantitatively differentiate the tumor models based on CD8 expression level. Conclusion Our work reveals the potential of this anti-human CD8 VHH [F-18]F-VHH5v2 to enable rapid and specific imaging of CD8(+) cells in the clinic.
引用
收藏
页码:679 / 691
页数:13
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