A large fraction of HLA class I ligands are proteasome-generated spliced peptides

  • Juliane Liepe
  • , Fabio Marino
  • , John Sidney
  • , Anita Jeko
  • , Daniel E Bunting
  • , Alessandro Sette
  • , Peter M Kloetzel
  • , Michael P H Stumpf
  • , Albert J R Heck
  • , Michele Mishto

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

The proteasome generates the epitopes presented on human leukocyte antigen (HLA) class I molecules that elicit CD8(+) T cell responses. Reports of proteasome-generated spliced epitopes exist, but they have been regarded as rare events. Here, however, we show that the proteasome-generated spliced peptide pool accounts for one-third of the entire HLA class I immunopeptidome in terms of diversity and one-fourth in terms of abundance. This pool also represents a unique set of antigens, possessing particular and distinguishing features. We validated this observation using a range of complementary experimental and bioinformatics approaches, as well as multiple cell types. The widespread appearance and abundance of proteasome-catalyzed peptide splicing events has implications for immunobiology and autoimmunity theories and may provide a previously untapped source of epitopes for use in vaccines and cancer immunotherapy.

Original languageEnglish
Pages (from-to)354-358
Number of pages5
JournalScience
Volume354
Issue number6310
DOIs
Publication statusPublished - 2016

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