Volume 2 Supplement 2

Abstracts from the 1st Immunotherapy of Cancer Conference (ITOC1)

Open Access

P32. High resolution mass spectrometry reveals the depth and diversity of HLA-I peptidomes

  • M Bassani-Sternberg1,
  • S Frankild2 and
  • M Mann1
Journal for ImmunoTherapy of Cancer20142(Suppl 2):P23

https://doi.org/10.1186/2051-1426-2-S2-P23

Published: 12 March 2014

T-cell responses against infected and cancer cells are initiated by recognition of HLA-I peptides (the peptidome) presented on the surface of nucleated cells. The repertoire of HLA-I peptides originates primarily from sampling the cytosolic degradation products of intracellular proteins. HLA-I peptides have been extensively studied in the last years because of their immediate use as immunotherapy based cancer vaccines. Even more advanced cell based therapeutic applications are being developed based on cancer specific HLA-I peptides. In this study, we used high resolution mass spectrometry and the MaxQuant bioinformatics environment to obtain a high accuracy and in-depth coverage of HLA peptidomes. HLA-I peptidomes were immuno-affinity purified from 10 cancer and primary cell lines. The unprecedented high number of thousands of identified HLA-I peptides per cell line enabled us to evaluate the known mechanisms governing peptidome presentation and to determine the proteome which is sampled for presentation. We envision that applying our methodology for analysing patients tumour samples will result in the discovery of new cancer specific peptides. Better immunotherapeutic modules could possibly be developed based on wider and more accurate repertoires of HLA-I peptides and they will increase the accessibility of these therapies for a larger cohort of patients.

Authors’ Affiliations

(1)
Max Planck Institute for Biochemistry, Proteomics and Signal Transduction
(2)
Faculty of Health, Novo Nordisk Foundation Center for Protein Research (CPR)

Copyright

© Bassani-Sternberg et al; licensee BioMed Central Ltd. 2014

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/2.0), 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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