PET Imaging of Sphingosine-1-Phosphate Receptor 1 with [18F]TZ4877 in Nonhuman Primates

TL;DR

This study evaluates [18F]TZ4877, a potential PET radiotracer for S1PR1, in nonhuman primates, finding it has fast kinetics but limited utility due to low free fraction.

Contribution

The study provides preclinical validation of [18F]TZ4877 for S1PR1 PET imaging in nonhuman primates.

Findings

[18F]TZ4877 showed fast kinetics and was best modeled by a reversible 2-tissue compartment model.

TZ82112 reduced [18F]TZ4877 VT/fP in a dose-dependent manner, while ponesimod and endotoxin had negligible effects.

The gallbladder was identified as the critical organ for radiation dose in dosimetry studies.

Abstract

The sphingosine-1-phosphate receptor-1 (S1PR1) is involved in regulating responses to neuroimmune stimuli. There is a need for S1PR1-specific radioligands with clinically suitable brain pharmcokinetic properties to complement existing radiotracers. This work evaluated a promising S1PR1 radiotracer, [18F]TZ4877, in nonhuman primates.

[18F]TZ4877 was produced via nucleophilic substitution of tosylate precursor with K[18F]/F− followed by deprotection. Brain PET imaging data were acquired with a Focus220 scanner in two Macaca mulatta (6, 13 years old) for 120–180 min following bolus injection of 118–163 MBq [18F]TZ4877, with arterial blood sampling and metabolite analysis to measure the parent input function and plasma free fraction (fP). Each animal was scanned at baseline, 15–18 min after 0.047–0.063 mg/kg of the S1PR1 inhibitor ponesimod, 33 min after 0.4–0.8 mg/kg of the S1PR1-specific compound TZ82112, and 167–195 min after 1 ng/kg of the immune stimulus endotoxin. Kinetic analysis with metabolite-corrected input function was performed to estimate the free fraction corrected total distribution volume (VT/fP). Whole-body dosimetry scans were acquired in 2 animals (1M, 1F) with a Biograph Vision PET/CT System, and absorbed radiation dose estimates were calculated with OLINDA.

[18F]TZ4877 exhibited fast kinetics that were described by the reversible 2-tissue compartment model. Baseline [18F]TZ4877 fP was low (< 1%), and [18F]TZ4877 VT/fP values were 233–866 mL/cm3. TZ82112 dose-dependently reduced [18F]TZ4877 VT/fP, while ponesimod and endotoxin exhibited negligible effects on VT/fP, possibly due to scan timing relative to dosing. Dosimetry studies identified the critical organs of gallbladder (0.42 (M) and 0.31 (F) mSv/MBq) for anesthetized nonhuman primate.

[18F]TZ4877 exhibits reversible kinetic properties, but the low fP value limits quantification with this radiotracer. S1PR1 is a compelling PET imaging target, and these data support pursuing alternative F-18 labeled radiotracers for potential future human studies.

Figures