A pair of congenic mice for imaging of transplants by positron emission tomography using anti-transferrin receptor nanobodies
Balligand, T.; Carpenet, C.; Olive Palau, S.; Jaspers, T.; Suresh, P.; Liu, X.; Medhi, H.; Lee, Y. H.; Rashidian, M.; De Strooper, B.; Ploegh, H. L.; Dewilde, M.
Show abstract
Two anti-transferrin receptor (TfR) nanobodies, VHH123 specific for mouse TfR and VHH188 specific for human TfR (huTfR) were used to track transplants non-invasively by PET/CT in mouse models, without the need for genetic modification of the transferred cells. We provide a comparison of the specificity and kinetics of the PET signals acquired when using nanobodies radiolabeled with 89Zr, 64Cu and 18F, and find that the chelation of the 89Zr and 64Cu radioisotopes to anti-TfR nanobodies results in radioisotope release upon endocytosis of the radiolabeled nanobodies. We used a knock-in mouse that expresses a TfR with a human ectodomain (huTfR +/+) as a source of bone marrow for transplants into C57BL/6 recipients and show that VHH188 detects such transplants by PET/CT. Conversely, C57BL/6 bone marrow and B16.F10 melanoma cell-line transplanted into huTfR +/+ recipients can be imaged with VHH123. In C57BL/6 mice impregnated by huTfR+/+ males we saw an intense VHH188 signal in the placenta, showing that TfR-specific VHHs accumulate at the placental barrier but do not enter the fetal tissue. We were unable to observe accumulation of the anti-TfR radiotracers in the central nervous system (CNS) by PET/CT but show evidence of CNS accumulation by radiospectrometry. The model presented here can be used to track many transplanted cell types by PET/CT, provided cells express TfR, as is typically the case for proliferating cells such as tumor lines.
Matching journals
The top 4 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- High-resolution positron emission microscopy of patient-derived tumor organoids 95%
- Target-responsive vasoactive probes for ultrasensitive molecular imaging 95%
- Priming versus propagating: distinct immune effects of an alpha- versus beta-particle emitting radiopharmaceutical when combined with immune checkpoint inhibition 94%
Similar papers in this journal
- Whole-body PET imaging of SIV using anti-Env probes fails to reveal regions of specific uptake in rhesus macaques 95%
- Non-invasive imaging of tau-targeted probe uptake by whole brain multi-spectral optoacoustic tomography 93%
- Combined, yet Separate: cocktails of carriers (not drugs) for α-particle therapy of solid tumors expressing moderate-to-low levels of targetable markers 93%
Similar papers in this journal
Similar papers in this journal
- Deciphering sources of PET signals in the tumor microenvironment of glioblastoma at cellular resolution 96%
- Efficient and multiplexed tracking of single cells using whole-body PET/CT 95%
- A Safe Harbor-Targeted CRISPR/Cas9 Homology Independent Targeted Integration (HITI) System for Multi-Modality Reporter Gene-Based Cell Tracking 94%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.