Sensitive Detection and Analysis of Neoantigen-Specific T Cell Populations from Tumors and Blood

Cell Rep. 2019 Sep 3;28(10):2728-2738.e7. doi: 10.1016/j.celrep.2019.07.106.

Abstract

Neoantigen-specific T cells are increasingly viewed as important immunotherapy effectors, but physically isolating these rare cell populations is challenging. Here, we describe a sensitive method for the enumeration and isolation of neoantigen-specific CD8+ T cells from small samples of patient tumor or blood. The method relies on magnetic nanoparticles that present neoantigen-loaded major histocompatibility complex (MHC) tetramers at high avidity by barcoded DNA linkers. The magnetic particles provide a convenient handle to isolate the desired cell populations, and the barcoded DNA enables multiplexed analysis. The method exhibits superior recovery of antigen-specific T cell populations relative to literature approaches. We applied the method to profile neoantigen-specific T cell populations in the tumor and blood of patients with metastatic melanoma over the course of anti-PD1 checkpoint inhibitor therapy. We show that the method has value for monitoring clinical responses to cancer immunotherapy and might help guide the development of personalized mutational neoantigen-specific T cell therapies and cancer vaccines.

Keywords: T cell receptor; cancer immunotherapy; microfluidics; nanotechnology; neoantigens.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antigens, Neoplasm / blood*
  • Biopsy
  • HEK293 Cells
  • Humans
  • Immunotherapy
  • Jurkat Cells
  • Kinetics
  • Lymphocytes, Tumor-Infiltrating / immunology
  • Magnetite Nanoparticles / chemistry
  • Major Histocompatibility Complex
  • Melanoma / blood*
  • Melanoma / immunology*
  • Melanoma / pathology
  • Melanoma / secondary
  • Nucleic Acids / metabolism
  • Programmed Cell Death 1 Receptor / immunology
  • Receptors, Antigen, T-Cell / metabolism
  • Reproducibility of Results
  • T-Lymphocytes / immunology*
  • Tomography, X-Ray Computed

Substances

  • Antigens, Neoplasm
  • Magnetite Nanoparticles
  • Nucleic Acids
  • Programmed Cell Death 1 Receptor
  • Receptors, Antigen, T-Cell