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

Front Nucl Med

Department of Radiology, Stanford University School of Medicine, Stanford, CA, United States.

Published: October 2023

AI Article Synopsis

  • * While all PET tracers accurately distinguish between diseased and normal tissues, some tracers are more suited for specific clinical applications based on their performance.
  • * Notably, head-to-tail cyclized peptide tracers do not accumulate in the gastrointestinal (GI) tract, contrasting with linear and disulfide-stabilized peptides, despite evidence of αvβ6 presence in the GI tract, indicating a need for more research in this area.

Article 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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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11440954PMC
http://dx.doi.org/10.3389/fnume.2023.1271208DOI Listing

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