Cell Reports (Sep 2019)

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

  • Songming Peng,
  • Jesse M. Zaretsky,
  • Alphonsus H.C. Ng,
  • William Chour,
  • Michael T. Bethune,
  • Jongchan Choi,
  • Alice Hsu,
  • Elizabeth Holman,
  • Xiaozhe Ding,
  • Katherine Guo,
  • Jungwoo Kim,
  • Alexander M. Xu,
  • John E. Heath,
  • Won Jun Noh,
  • Jing Zhou,
  • Yapeng Su,
  • Yue Lu,
  • Jami McLaughlin,
  • Donghui Cheng,
  • Owen N. Witte,
  • David Baltimore,
  • Antoni Ribas,
  • James R. Heath

Journal volume & issue
Vol. 28, no. 10
pp. 2728 – 2738.e7

Abstract

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Summary: 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. : Peng et al. report a sensitive method to detect tumor-associated neoantigen-specific T cells. Neoantigens and fluorescent DNA barcodes, presented on nanoparticle scaffolds, permit multiplex capture and analysis of specific T cell populations from blood or tumor. Neoantigen-specific T cell numbers track tumor volume in a melanoma patient responding to immunotherapy. Keywords: neoantigens, cancer immunotherapy, nanotechnology, microfluidics, T cell receptor