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.

PubMed

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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