Noninvasive Evaluation of Tumoral PD-L1 Using a Novel 99m Tc-Labeled Nanobody Tracer with Rapid Renal Clearance.
Biao HuXiaopan MaLinqing ShiTianyu LiuLiqiang LiMeinan YaoChenzhen LiBing JiaPublished in: Molecular pharmaceutics (2024)
The expression level of PD-L1 in tumor tissue is considered one of the effective biomarkers to guide PD-1/PD-L1 therapy. Quantifying whole-body PD-L1 expression by SPECT imaging may help in selecting patients that potentially respond to PD-1/PD-L1 therapy. Nanobody is the smallest antibody fragment with antigen-binding ability that is well suited for radionuclide imaging. Nevertheless, high retention of radioactivity in the kidney may limit its clinical translation. The present study aimed to screen, design, and prepare a nanobody-based SPECT probe with rapid renal clearance to evaluate the PD-L1 expression level in vivo noninvasively. A phage library was constructed by immunizing alpaca with recombinant human PD-L1 protein, and 17 anti-PD-L1 nanobodies were screened by the phage display technique. After sequence alignment and flow cytometry analysis, APN09 was selected as the candidate nanobody, and a GGGC chelator was attached to its C-terminus for 99m Tc labeling to prepare a SPECT imaging probe. The affinity and specificity of 99m Tc-APN09 were evaluated by protein and cell-binding experiments, and SPECT imaging and biodistribution were performed in a mouse model with bilateral transplantation of A549 and A549 PD-L1 tumors. The ability of 99m Tc-APN09 to quantify the PD-L1 expression level in vivo was validated in tumor models with different PD-L1 expression levels. 99m Tc-APN09 had a radiochemical purity higher than 99% and a binding equilibrium dissociation constant of 21.44 ± 1.65 nM with hPD-L1, showing high affinity. SPECT imaging results showed that 99m Tc-APN09 could efficiently detect PD-L1-positive tumors within 0.5 h, and the quantitative results of SPECT were well correlated with the expression level of PD-L1 in cell lines. SPECT imaging and biodistribution results also showed that 99m Tc-APN09 was rapidly cleared from the kidney in 2 h postinjection. 99m Tc-APN09 was a simple and stable tool for visualizing PD-L1 expression in the whole body. In addition, due to its significant reduction in renal retention, it has better prospects for clinical translation.
Keyphrases
- high resolution
- pet ct
- binding protein
- mouse model
- poor prognosis
- flow cytometry
- stem cells
- recombinant human
- chronic kidney disease
- fluorescence imaging
- quantum dots
- mass spectrometry
- prognostic factors
- photodynamic therapy
- molecular dynamics
- ejection fraction
- molecular dynamics simulations
- peritoneal dialysis
- loop mediated isothermal amplification
- sensitive detection