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Updated: Sep 20, 2025

Pretargeted Radioimmunotherapy Based on the Inverse Electron Demand Diels-Alder Reaction
Published on: January 29, 2019
Development of a Novel Engineered Antibody Format for PSMA-Targeted Radionuclide Therapy
Nicholas L Fletcher1,2, Zachary H Houston1, Peter G Chandler3
1Centre for Advanced Imaging, Australian Institute for Bioengineering & Nanotechnology, University of Queensland, St. Lucia, Brisbane, Queensland 4072, Australia.
Abstract:
Prostate cancer remains a prevalent and lethal malignancy across the globe. Despite ongoing advances in therapeutic approaches, these remain ineffective, and new treatments are drastically needed. Prostate-specific membrane antigen (PSMA)-targeted radionuclide therapy is a well-developed approach for prostate cancer treatment; however, current small molecule and antibody carriers for molecular radiotherapy each have drawbacks in their biodistribution and consequent side effects as highlighted in current clinical trials. To address this, we developed an approach to bioengineer the well clinically validated antibody carrier HuJ591 to yield an engineered, full-length antibody construct that achieves the beneficial fast pharmacokinetic profile of small molecule carriers alongside the enhanced tumor targeting and reduced renal toxicity of antibody carriers. We report here a rational design process to produce a novel humanized PSMA-targeting antibody designed for the delivery of radiation with abrogated FcRn recycling that aims to reduce blood circulation time and minimize systemic exposure. We demonstrate that these IgG-based constructs retain the favorable properties of HuJ591, such as inherent protein stability, expression in systems compatible with industrial manufacture, and comparable, highly specific PSMA-binding characteristics. We then radiolabeled constructs with the diagnostic radionuclide 64Cu as a surrogate for therapeutic radionuclide payloads and undertook a proof-of-concept preclinical imaging study to probe the resulting in vivo behaviors. This demonstrated the success of this design strategy to yield the intended in vivo and radiopharmaceutical characteristics, with the resulting construct being rapidly cleared from circulation over 3 days. Together, this study demonstrates the rational design of a novel targeting antibody platform for PSMA-expressing tumors with reduced systemic exposure. Such a platform is extremely promising for future radiotherapeutic delivery approaches, whereby effective tumor treatment can be achieved while mitigating potential hematologic toxicity observed with standard antibody delivery approaches.
Insights
Researchers engineered a novel antibody for prostate-specific membrane antigen (PSMA)-targeted radionuclide therapy. This new construct offers faster clearance and reduced side effects for improved prostate cancer treatment.
Area of Science:
- Oncology
- Radiopharmaceutical Science
- Immunotherapy
Background:
- Prostate cancer is a leading cause of cancer death worldwide, necessitating improved therapeutic strategies.
- Current prostate-specific membrane antigen (PSMA)-targeted radionuclide therapies using small molecules or antibodies have limitations in biodistribution and side effects.
- There is a critical need for advanced treatments that enhance efficacy while minimizing toxicity.
Purpose of the Study:
- To develop an improved antibody carrier for PSMA-targeted radionuclide therapy.
- To engineer a full-length antibody construct that combines the pharmacokinetic benefits of small molecules with the targeting advantages of antibodies.
- To reduce systemic exposure and potential toxicities associated with antibody-based radiotherapeutics.
Main Methods:
- Rational design of a novel humanized PSMA-targeting antibody with abrogated FcRn recycling.
- Assessment of protein stability, manufacturability, and PSMA-binding affinity of the engineered antibody.
- Radiolabeling with 64Cu for preclinical in vivo imaging and pharmacokinetic evaluation.
Main Results:
- The engineered IgG-based antibody construct demonstrated high specificity for PSMA.
- The construct exhibited favorable protein stability and compatibility with industrial manufacturing.
- Preclinical imaging confirmed rapid clearance from circulation within 3 days, indicating reduced systemic exposure.
Conclusions:
- The rational design successfully yielded a novel antibody platform for PSMA-expressing tumors.
- This platform offers reduced systemic exposure compared to standard antibody delivery methods.
- The engineered antibody holds significant promise for future radiotherapeutic delivery, potentially mitigating hematologic toxicities.
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