Bioorthogonal masking of circulating antibody-TCO groups using tetrazine-functionalized dextran polymers Journal Article

Authors: Meyer, J. P.; Tully, K. M.; Jackson, J.; Dilling, T. R.; Reiner, T.; Lewis, J. S.
Article Title: Bioorthogonal masking of circulating antibody-TCO groups using tetrazine-functionalized dextran polymers
Abstract: Pretargeting strategies have gained popularity for the in vivo imaging and therapy of cancer by combining antibodies with small molecule radioligands. In vivo recombination of both moieties can be achieved using the bioorthogonal inverse electron demand Diels-Alder (IEDDA) chemistry between tetrazine (Tz) and trans-cyclooctene (TCO). An issue that arises with pretargeting strategies is that while part of the antibody dose accumulates at antigen-expressing tumor tissue, there is a significant portion of the injected antibody that remains in circulation, causing a reduction in target-to-background ratios. Herein, we report the development of a novel TCO scavenger, the masking agent DP-Tz. DP-Tz is based on Tz-modified dextran polymers (DP, MW = 0.5-2 MDa). Large dextran polymers were reported to exhibit low penetration of tumor vasculature and appeared nontoxic, nonimmunogenic, and easily modifiable. Our newly developed masking agent deactivates the remaining TCO-moieties on the circulating mAbs yet does not impact the tumor uptake of the Tz-radioligand. In pretargeting studies utilizing a 68Ga-labeled tetrazine radioligand ([68Ga]Ga-NOTA-PEG11-tetrazine), DP-Tz constructs (Tz/DP ratios of 62-254) significantly increased TTB ratios from 0.8 ± 0.3 (control cohorts) to up to 5.8 ± 2.3 at 2 h postinjection. Tumor tissue delineation in PET imaging experiments employing DP-Tz is significantly increased compared to control. Uptake values of other significant organs, such as heart, lungs, pancreas, and stomach, were decreased on average by 2-fold when using DP-Tz. Overall, pretargeting experiments utilizing DP-Tz showed significantly improved tumor delineation, enhanced PET image quality, and reduced uptake in vital organs. We believe that this new masking agent is a powerful new addition to the IEDDA-based pretargeting tool box and, due to its properties, an excellent candidate for clinical translation. © 2018 American Chemical Society.
Keywords: controlled study; unclassified drug; nonhuman; positron emission tomography; colorectal cancer; mouse; animal tissue; dextran; image quality; high performance liquid chromatography; tumor vascularization; antibody; gallium 68; synthesis; zirconium 89; scavenger; size exclusion chromatography; tetrazine derivative; article; trans cyclooctene
Journal Title: Bioconjugate Chemistry
Volume: 29
Issue: 2
ISSN: 1043-1802
Publisher: American Chemical Society  
Date Published: 2018-02-21
Start Page: 538
End Page: 545
Language: English
DOI: 10.1021/acs.bioconjchem.8b00028
PROVIDER: scopus
PUBMED: 29378403
PMCID: PMC6004324
Notes: Article -- Export Date: 2 April 2018 -- Source: Scopus
Citation Impact
MSK Authors
  1. Jason S Lewis
    360 Lewis
  2. Thomas Reiner
    123 Reiner
  3. Jan-Philip   Meyer
    7 Meyer
  4. Thomas R Dilling
    10 Dilling
  5. Kathryn Margaret Tully
    8 Tully