Endosomal processing for antigen presentation mediated by CD1 and Class I major histocompatibility complex: roads to display or destruction

Marianne Boes*, Arie J. Stoppelenburg, Fenna C. M. Sille

*Corresponding author for this work

Research output: Contribution to journalLiterature reviewpeer-review

Abstract

The presentation of antigen in a form that can be recognized by T lymphocytes of the immune system requires antigen processing and association of antigen-derived fragments with molecules encoded by the major histocompatibility complex (MHC) locus or by the CD1 locus. Much emphasis on antigen processing and presentation in the last decades has focused on what we consider 'conventional routes' of antigen processing and presentation, whereby extracellular antigens are processed for presentation via Class II MHC complexes and cytosolic antigens are presented as peptide-Class I MHC complexes. We here highlight two other pathways in myeloid dendritic cells, those of lipid antigen presentation in association with CD1 and of peptide cross-presentation via Class I MHC complexes. Some pathogens evade immune recognition through inhibition of antigen presentation of phagosomal origin. Deviations in endosomal antigen processing and presentation are also seen in individuals suffering from glycosphingolipid lysosomal lipid storage diseases. We summarize recent developments in the endosomal antigen processing and presentation pathway, for display as lipid-CD1 complexes to natural killer T cells and as peptide-Class I MHC complexes to CD8 T cells.

Original languageEnglish
Pages (from-to)163-170
Number of pages8
JournalImmunology
Volume127
Issue number2
DOIs
Publication statusPublished - Jun 2009

Keywords

  • CD1d
  • cross-presentation
  • endosome
  • major histocompatibility complex Class I
  • myeloid dendritic cell
  • MHC CLASS-II
  • DENDRITIC CELL MATURATION
  • TRIGLYCERIDE TRANSFER PROTEIN
  • VIRAL DANGER SIGNALS
  • TOLL-LIKE RECEPTORS
  • CROSS-PRESENTATION
  • T-CELLS
  • MYCOBACTERIUM-TUBERCULOSIS
  • NKT CELLS
  • ENDOPLASMIC-RETICULUM

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