Back to Search Start Over

Non-invasive PET imaging of liver fibrogenesis using a RESCA-conjugated Affibody molecule

Authors :
Wegrzyniak, Olivia
Lechi, Francesco
Mitran, Bogdan
Cheung, Pierre
Bitzios, Athanasios
Persson, Jonas
Löfblom, John
Nordström, Helena
Eriksson, Jonas
Frejd, Fredrik
Korsgren, Olle
Zhang, Bo
Eriksson, Olof
Wegrzyniak, Olivia
Lechi, Francesco
Mitran, Bogdan
Cheung, Pierre
Bitzios, Athanasios
Persson, Jonas
Löfblom, John
Nordström, Helena
Eriksson, Jonas
Frejd, Fredrik
Korsgren, Olle
Zhang, Bo
Eriksson, Olof
Publication Year :
2024

Abstract

Non-invasive assessment of fibrogenic activity, rather than fibrotic scars, could significantly improve the management of fibrotic diseases and the development of anti-fibrotic drugs. This study explores the potential of an Affibody molecule (Z09591) labeled with the Al(18)F-restrained complexing agent (RESCA) method as a tracer for the non-invasive detection of fibrogenic cells. Z09591 was functionalized with the RESCA chelator for direct labeling with [18F]AlF. 18 F]AlF. In vivo positron emission tomography/magnetic resonance imaging scans on U-87 tumor-bearing mice exhibited high selectivity of the resulting radiotracer, [18F]AlF-RESCA-Z09591, 18 F]AlF-RESCA-Z09591, for platelet-derived growth factor receptor b (PDGFRb), b ), with minimal non-specific background uptake. Evaluation in a mouse model with carbon tetrachloride-induced fibrotic liver followed by a disease regression phase, revealed the radiotracer's high affinity and specificity for fibrogenic cells in fibrotic livers (standardized uptake value [SUV] 0.43 +/- 0.05), with uptake decreasing during recovery (SUV 0.29 +/- 0.03) (p p < 0.0001). [18F]AlF-RESCA-Z09591 18 F]AlF-RESCA-Z09591 accurately detects PDGFRb, b, offering noninvasive assessment of fibrogenic cells and promising applications in precise liver fibrogenesis diagnosis, potentially contributing significantly to anti-fibrotic drug development.

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1457291379
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1016.j.isci.2024.109688