Kimura Richard H, Iagaru Andrei, Guo H Henry
Department of Radiology, Stanford University School of Medicine, Stanford, CA, United States.
Front Nucl Med. 2023 Oct 9;3:1271208. doi: 10.3389/fnume.2023.1271208. eCollection 2023.
This mini review of clinically-evaluated integrin αvβ6 PET-tracers reveals distinct differences in human-biodistribution patterns between linear peptides, including disulfide-stabilized formats, compared to head-to-tail cyclized peptides. All PET tracers mentioned in this mini review were able to delineate disease from normal tissues, but some αvβ6 PET tracers are better than others for particular clinical applications. Each αvβ6 PET tracer was validated for its ability to bind integrin αvβ6 with high affinity. However, all the head-to-tail cyclized peptide PET-tracers reviewed here did not accumulate in the GI-tract, in striking contrast to the linear and disulfide-bonded counterparts currently undergoing clinical evaluation in cancer, IPF and long COVID. Multiple independent investigators have reported the presence of β6 mRNA as well as αvβ6 protein in the GI-tract. Currently, there remains further need for biochemical, clinical, and structural data to satisfactorily explain the state-of-the-art in human αvβ6-imaging.
这篇对经临床评估的整合素αvβ6正电子发射断层显像(PET)示踪剂的小型综述揭示,与头对尾环化肽相比,线性肽(包括二硫键稳定形式)在人体生物分布模式上存在明显差异。本小型综述中提到的所有PET示踪剂都能够区分病变组织与正常组织,但某些αvβ6 PET示踪剂在特定临床应用中比其他示踪剂表现更佳。每种αvβ6 PET示踪剂都经过验证,具有与整合素αvβ6高亲和力结合的能力。然而,本文综述的所有头对尾环化肽PET示踪剂在胃肠道中均无积聚,这与目前正在癌症、特发性肺纤维化和长期新冠临床评估中的线性及二硫键连接的对应物形成鲜明对比。多个独立研究团队报告了胃肠道中存在β6信使核糖核酸(mRNA)以及αvβ6蛋白。目前,仍需要更多生化、临床和结构数据来令人满意地解释人类αvβ6成像的现状。