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Post-translationally modified T cell epitopes: immune recognition and immunotherapy

Journal

JOURNAL OF MOLECULAR MEDICINE-JMM
Volume 87, Issue 11, Pages 1045-1051

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00109-009-0526-4

Keywords

Post-translational modification; Immunity; T cell receptor; Major histocompatibility antigen complex

Funding

  1. NHMRC [491117, 508927]
  2. NIH [GM057428-06]

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The functionality of proteins is greatly extended by a diverse array of post-translational modifications (PTMs), many of which are recognized by the immune system. Notably, a significant proportion of peptides presented to T cells by the major histocompatibility complex in vivo are post-translationally modified. Since the cellular mechanisms that introduce and control protein modifications can differ between health and disease, the associated changes in antigen presentation have the potential to alter immune responses. A number of such situations have been implicated with infection, inflammation, autoimmune disease, and cancer, and the investigation of PTMs that affect antigen recognition has provided insight in disease progression as well as raising prospects for novel approaches in immunotherapy.

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