Mini review of first-in-human integrin αvβ6 PET tracers

Richard H. Kimura, Andrei Iagaru, H. Henry Guo
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Abstract

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.
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首次人用整合素αvβ6 PET示踪剂的综述
这项对临床评估的整合素αvβ6 pet示踪剂的小型综述揭示了线性肽(包括二硫稳定格式)与从头到尾环化肽在人体生物分布模式上的明显差异。在这篇小型综述中提到的所有PET示踪剂都能够从正常组织中描绘疾病,但在特定的临床应用中,一些αvβ6 PET示踪剂比其他示踪剂更好。每个αvβ6 PET示踪剂都具有高亲和力结合整合素αvβ6的能力。然而,本文综述的所有首尾环化肽pet示踪剂均未在胃肠道中积累,这与目前正在癌症、IPF和长COVID中进行临床评估的线性和二硫键化示踪剂形成鲜明对比。多个独立研究人员报道了gi道中β6 mRNA和αvβ6蛋白的存在。目前,仍需要进一步的生化、临床和结构数据来令人满意地解释人类αvβ6成像的最新进展。
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