Startseite Molecular challenges imposed by MHC-I restricted long epitopes on T cell immunity
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Molecular challenges imposed by MHC-I restricted long epitopes on T cell immunity

  • Tracy M. Josephs , Emma J. Grant und Stephanie Gras EMAIL logo
Veröffentlicht/Copyright: 23. Juni 2017

Abstract

It has widely been accepted that major histocompatibility complex class I molecules (MHC-I) are limited to binding small peptides of 8–10 residues in length. However, this consensus has recently been challenged with the identification of longer peptides (≥11 residues) that can also elicit cytotoxic CD8+ T cell responses. Indeed, a growing number of studies demonstrate that these non-canonical epitopes are important targets for the immune system. As long epitopes represent up to 10% of the peptide repertoire bound to MHC-I molecules, here we review their impact on antigen presentation by MHC-I, TCR recognition, and T cell immunity.

Acknowledgements

This work has been supported by the Australian Research Council and the National Health and Medical Research Council. E.J.G. was supported by an NHMRC CJ Martin Early Career Fellowship and S.G. was supported by an ARC Future Fellowship (FT120100416).

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Received: 2016-10-10
Accepted: 2017-1-25
Published Online: 2017-6-23
Published in Print: 2017-8-28

©2017 Walter de Gruyter GmbH, Berlin/Boston

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