Overview

Despite the potential of immunotherapy (IO), a minority of patients respond to treatment. As effective IO treatments enhance T cell infiltration and activation, understanding T cell behavior is paramount for developing successful treatment strategies. Biopsies are used to assess T cell states, but are invasive and may not accurately reflect tumor burden. Positron emission tomography (PET) imaging holds promise as a non-invasive, comprehensive means for evaluating T cell activity.

The iRelate project aims to assess T cell presence and activation state using two PET ligands in clinical development: [89Zr]Zr-Df-IAB22M2C, a CD8a-targeting minibody developed by ImaginAb; and [18F]FAraG, a mitochondrial enzyme-targeting small molecule developed by CellSight. Using both PET tracers will enable characterization of tracer uptakes in tumor tissue and T-cell-rich organs and is expected to provide information on unique and additive capacities of these tracers. This work is intended to serve as a foundation for defining potential context of use for PET biomarkers, and to support the development and selection of successful IO treatment strategies.

Goals
  • Establish the extent to which [18F] F-AraG and [89Zr]Crefmirlimab tracers provide either overlapping or complementary uptake in tumors and T cell rich organs (e.g., spleen, lymph nodes)

  • Correlate the uptake and distribution of [18F]F-AraG and [89Zr]Crefmirlimab with the presence of CD8+ cells and T cell activation features as assessed in resected tissues

Partners

PUBLIC SECTOR PARTNERS
  • National Cancer Institute (NCI)
  • U.S. Food and Drug Administration (FDA)
ACADEMIC PARTNERS
  • Amsterdam University Medical Center
PRIVATE SECTOR PARTNERS
  • Boehringer Ingelheim
  • Genmab
PROJECT SUPPORT
  • CellSight Technologies, Inc.
  • ImaginAb
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