Single-cell-guided identification of logic-gated antigen combinations for designing effective and safe CAR therapy

Sanna Madan1,2, Tian-Gen Chang1, Alexandra R Harris3,4

  • 1Cancer Data Science Laboratory, National Cancer Institute, National Institutes of Health, Bethesda, MD USA.

Insights

LogiCAR designer, a computational tool, creates logic-gated chimeric antigen receptor (CAR) T-cell circuits for solid tumors. Personalized CAR circuits show significantly higher efficacy than shared ones, offering a new path for cancer immunotherapy.

Area of Science:

  • Immunology
  • Computational Biology
  • Oncology

Background:

  • Chimeric antigen receptor (CAR) T-cell therapy shows promise in hematological malignancies but faces limitations in solid tumors due to antigen heterogeneity and off-tumor toxicities.
  • Existing CAR T-cell therapies often rely on single targets, which are insufficient for effectively treating solid tumors.

Purpose of the Study:

  • To develop and validate LogiCAR designer, a computational approach for designing logic-gated CAR T-cell circuits.
  • To identify cancer-specific antigen circuits that maximize tumor cell targeting while minimizing off-tumor effects.
  • To evaluate the efficacy and safety of both shared and individualized CAR circuits.

Main Methods:

  • Utilized single-cell transcriptomics data from patient tumors to identify antigen circuits with logic gates (AND, OR, NOT).
  • Applied LogiCAR designer to a large dataset of breast cancer samples (∼2 million cells) to identify potential CAR circuits.
  • Conducted comprehensive safety profiling of candidate circuits at RNA and protein levels across major tissues.

Main Results:

  • LogiCAR designer identified logic-gated CAR circuits with improved tumor-targeting efficacy and safety compared to existing therapies.
  • Shared CAR circuits demonstrated moderate efficacy, while individualized circuits showed significantly higher tumor-targeting potential.
  • Personalized CAR circuits achieved estimated tumor-targeting efficacy equivalent to complete response in 76% of patients.

Conclusions:

  • The quality of current CAR T-cell solutions for solid tumors needs improvement.
  • Individually tailored CAR circuits offer superior tumor-targeting efficacy compared to shared circuits.
  • LogiCAR designer provides a data-driven platform for designing safe and effective CAR-based immunotherapies.

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