Cutting edge: Class I presentation of host peptides following HIV infection

  • Heather D. Hickman
  • , Angela D. Luis
  • , Wilfried Bardet
  • , Rico Buchli
  • , Casey L. Battson
  • , Michael H. Shearer
  • , Kenneth W. Jackson
  • , Ronald C. Kennedy
  • , William H. Hildebrand

Research output: Contribution to journalArticlepeer-review

67 Scopus citations

Abstract

Class I MHC molecules bind intracellular peptides for presentation to cytotoxic T lymphocytes. Identification of peptides presented by class I molecules during infection is therefore a priority for detecting and targeting intracellular pathogens. To understand which host-encoded peptides distinguish HIV-infected cells, we have developed a mass spectrometric approach to characterize HLA-B*0702 peptides unique to or up-regulated on infected T cells. In this study, we identify 15 host proteins that are differentially presented on infected human T cells. Pep-tides with increased expression on HIV-infected cells were derived from multiple categories of cellular proteins including RNA binding proteins and cell cycle regulatory proteins. Therefore, comprehensive analysis of the B*0702 peptide repertoire demonstrates that marked differences in host protein presentation occur after HIV infection.

Original languageEnglish
Pages (from-to)22-26
Number of pages5
JournalJournal of Immunology
Volume171
Issue number1
DOIs
StatePublished - Jul 1 2003

Funding

Funder number
T32AI007633

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

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