Imaging Demyelinated Axons After Spinal Cord Injuries with PET Tracer [18F]3F4AP.

Spinal cord injuries (SCIs) often lead to lifelong disability. Among the various types of injuries, incomplete and discomplete injuries, where some axons remain intact, offer potential for recovery. However, demyelination of these spared axons can worsen disability. Demyelination is a reversible phenomenon, and drugs such as 4-aminopyridine (4AP), which target K+ channels in demyelinated axons, show that conduction can be restored. Yet, accurately assessing and monitoring demyelination after SCI remains challenging because of the lack of suitable imaging methods. In this study, we introduce a novel approach using the PET tracer, 3-[18F]fluoro-4-aminopyridine ([18F]3F4AP), specifically targeting K+ channels in demyelinated axons for SCI imaging. Methods: Rats with incomplete contusion injuries were imaged with [18F]3F4AP PET up to 1 mo after injury, followed by further validation of PET imaging results with autoradiography and immunohistochemistry of postmortem spinal cord tissue. A proof-of-concept study in 2 human subjects with incomplete injuries of different severities and etiologies was also performed. Results: [18F]3F4AP PET of SCI rats revealed a more than 2-fold increase in tracer binding highly localized to the injured segment of the cord at 7 d after injury relative to baseline (SUV ratio = 2.49 ± 0.09 for 7 d after injury vs. 1.14 ± 0.10 for baseline), revealing [18F]3F4AP's exceptional sensitivity to injury and its ability to detect temporal changes. Autoradiography, histology, and immunohistochemistry confirmed [18F]3F4AP's targeting of demyelinated axons. In humans, [18F]3F4AP differentiated between a severe and a largely recovered incomplete injury, indicating axonal loss and demyelination, respectively. Moreover, alterations in tracer delivery were evident on dynamic PET images, suggestive of differences in spinal cord blood flow between the injuries. Conclusion: [18F]3F4AP demonstrates efficacy in detecting incomplete SCI in both animal models and humans. The potential for monitoring post-SCI demyelination changes and response to therapy underscores the utility of [18F]3F4AP in advancing our understanding and management of SCI.