Preclinical antibody-PET imaging of PD-L1

Emma L Brown1, Rachel A DeWeerd1,2, Abbey Zidel1

  • 1Department of Radiology, Mallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO, United States.

PubMed

Insights

Positron emission tomography (PET) imaging visualizes Programmed cell death protein-1 ligand-1 (PD-L1) expression in real-time. This approach aids in predicting cancer immunotherapy response and understanding tumor heterogeneity.

Area of Science:

  • Oncology
  • Immunotherapy
  • Radiochemistry

Background:

  • Immune checkpoint inhibitors targeting Programmed cell death protein-1/ligand-1 (PD-1/PD-L1) have revolutionized cancer therapy.
  • Accurate patient selection for PD-1/PD-L1 blockade remains a challenge due to limitations of biopsy-based diagnostics in capturing tumor heterogeneity.
  • Current methods fail to fully predict response, as some PD-L1-negative tumors benefit from immunotherapy, while some PD-L1-positive tumors do not.

Purpose of the Study:

  • To review recent advancements in PD-1/PD-L1 targeted positron emission tomography (PET) imaging for cancer immunotherapy.
  • To highlight the expansion of preclinical models and novel anti-PD-L1 antibodies/fragments for immunoPET development.
  • To discuss the utility of these tools in assessing the spatial and temporal heterogeneity of PD-L1 expression.

Main Methods:

  • Review of PD-1/PD-L1 targeted immunoPET studies published in the last four years.
  • Focus on preclinical tumor models and the development of anti-PD-L1 antibodies and antibody fragments for PET imaging.
  • Analysis of how these imaging agents and models can address PD-L1 expression heterogeneity.

Main Results:

  • The development and application of zirconium-89 labeled anti-PD-L1 antibodies have enabled in vivo visualization of PD-L1 expression.
  • Expansion of preclinical models and antibody-based targeting agents for PD-L1 immunoPET.
  • Demonstration of immunoPET's potential to assess real-time, whole-tumor PD-L1 heterogeneity.

Conclusions:

  • PD-1/PD-L1 targeted immunoPET offers a promising strategy for non-invasive assessment of PD-L1 expression and heterogeneity.
  • This technology has the potential to improve patient selection for immune checkpoint inhibitor therapy.
  • Further development of preclinical models and imaging agents will enhance the clinical utility of PD-L1 immunoPET.