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MIT-Dana-Farber Team Identifies Cryptic Peptides as Novel Targets for Pancreatic Cancer Therapy

Preclinical research shows engineered T cells targeting tumor-specific peptides slow pancreatic tumor growth and destroy patient-derived organoids.

“Pancreas cancer is one of the most challenging cancers to treat. This study identifies an unexpected vulnerability in pancreas cancer cells that we may be able to exploit therapeutically,” says Tyler Jacks.

Overview

  • Researchers discovered approximately 500 cryptic peptides uniquely expressed in pancreatic tumors, offering potential targets for immunotherapy.
  • Cryptic peptides, derived from non-coding genomic regions, were identified using immunopeptidomics and organoid models from patient samples.
  • Engineered T cells targeting these peptides significantly slowed tumor growth in mice and destroyed pancreatic tumor organoids in vitro.
  • This research marks the first demonstration of T cells effectively targeting cryptic peptides in pancreatic cancer, a notoriously treatment-resistant malignancy.
  • Efforts are underway to develop vaccines and other therapies based on these findings, though human trials remain several years away.