Volume 3 Supplement 2

30th Annual Meeting and Associated Programs of the Society for Immunotherapy of Cancer (SITC 2015)

Open Access

Immunogenicity of recurrent mutations in MYD88 and EZH2 in non-Hodgkin lymphomas

  • Julie S Nielsen1,
  • Andrew R Chang1,
  • Darin A Wick1,
  • Colin G Sedgwick1,
  • Zusheng Zong2,
  • Andrew J Mungall3,
  • Bemuluyigza Baraki2,
  • Natalie Kinloch2,
  • Zabrina L Brumme2,
  • Steven P Treon4,
  • Joseph M Connors3,
  • Randy D Gascoyne3,
  • John R Webb1,
  • Brian R Berry5,
  • Ryan D Morin2,
  • Nicol Macpherson1 and
  • Brad H Nelson1
Journal for ImmunoTherapy of Cancer20153(Suppl 2):P386

https://doi.org/10.1186/2051-1426-3-S2-P386

Published: 4 November 2015

A fundamental challenge in cancer genomics is to design effective, personalized treatments based on the mutational profiles of tumors. Pharmacological targeting of the numerous aberrant pathways found in individual tumors remains exceedingly challenging, but T cell-based therapies are an attractive alternative because of the enormous diversity and exquisite specificity of antigen recognition. We assessed the immunogenicity of three common driver mutations in human lymphoma – MYD88L265P, EZH2Y641N, and EZH2Y641F – to evaluate their suitability as targets for immunotherapy. Antigen presenting cells were loaded with overlapping peptide libraries containing each mutation and used to stimulate autologous T cells from healthy donors and lymphoma patients. Stimulated T cells were screened by interferon-gamma ELISPOT for reactivity to mutant versus wildtype peptides as well as full-length proteins. All three peptide libraries elicited T cell responses from multiple donors representing diverse HLA haplotypes. Moreover, we identified peptides from MYD88L265P and EZH2Y641N that were naturally processed and presented, and the corresponding T cell responses were specific for mutant proteins. Thus, MYD88L265P and EZH2Y641N both represent compelling antigens for immunotherapy of lymphoma patients. Funding was provided by the BC Cancer Foundation, the Canadian Cancer Society, and the Waldenstrom's Macroglobulinemia Foundation of Canada.

Authors’ Affiliations

(1)
BC Cancer Agency
(2)
Simon Fraser University
(3)
BC Cancer Agency
(4)
Dana-Farber Cancer Institute
(5)
University of British Columbia

Copyright

© Nielsen et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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