Activated tissue resident memory T-cells (CD8+CD103+CD39+) uniquely predict survival in left sided "immune-hot" colorectal cancers. Academic Article uri icon

Overview

abstract

  • INTRODUCTION: Characterization of the tumour immune infiltrate (notably CD8+ T-cells) has strong predictive survival value for cancer patients. Quantification of CD8 T-cells alone cannot determine antigenic experience, as not all infiltrating T-cells recognize tumour antigens. Activated tumour-specific tissue resident memory CD8 T-cells (TRM) can be defined by the co-express of CD103, CD39 and CD8. We investigated the hypothesis that the abundance and localization of TRM provides a higher-resolution route to patient stratification. METHODS: A comprehensive series of 1000 colorectal cancer (CRC) were arrayed on a tissue microarray, with representative cores from three tumour locations and the adjacent normal mucosa. Using multiplex immunohistochemistry we quantified and determined the localization of TRM. RESULTS: Across all patients, activated TRM were an independent predictor of survival, and superior to CD8 alone. Patients with the best survival had immune-hot tumours heavily infiltrated throughout with activated TRM. Interestingly, differences between right- and left-sided tumours were apparent. In left-sided CRC, only the presence of activated TRM (and not CD8 alone) was prognostically significant. Patients with low numbers of activated TRM cells had a poor prognosis even with high CD8 T-cell infiltration. In contrast, in right-sided CRC, high CD8 T-cell infiltration with low numbers of activated TRM was a good prognosis. CONCLUSION: The presence of high intra-tumoural CD8 T-cells alone is not a predictor of survival in left-sided CRC and potentially risks under treatment of patients. Measuring both high tumour-associated TRM and total CD8 T-cells in left-sided disease has the potential to minimize current under-treatment of patients. The challenge will be to design immunotherapies, for left-sided CRC patients with high CD8 T-cells and low activate TRM,that result in effective immune responses and thereby improve patient survival.

authors

  • Talhouni, Shahd
  • Fadhil, Wakkas
  • Mongan, Nigel P
  • Field, Lara
  • Hunter, Kelly
  • Makhsous, Sogand
  • Maciel-Guerra, Alexandre
  • Kaur, Nayandeep
  • Nestarenkaite, Ausrine
  • Laurinavicius, Arvydas
  • Willcox, Benjamin E
  • Dottorini, Tania
  • Spendlove, Ian
  • Jackson, Andrew M
  • Ilyas, Mohammad
  • Ramage, Judith M

publication date

  • May 11, 2023

Research

keywords

  • Colorectal Neoplasms
  • Memory T Cells

Identity

PubMed Central ID

  • PMC10213916

Scopus Document Identifier

  • 85160032408

Digital Object Identifier (DOI)

  • 10.3389/fimmu.2023.1057292

PubMed ID

  • 37251410

Additional Document Info

volume

  • 14