Human cytomegalovirus protein pp65 mediates accumulation of HLA-DR in lysosomes and destruction of the HLA-DR alpha-chain

Blood. 2003 Jun 15;101(12):4870-7. doi: 10.1182/blood-2002-05-1504. Epub 2003 Feb 27.

Abstract

Human cytomegalovirus (HCMV) has developed multiple strategies to escape immune recognition. Here, we demonstrate that HCMV down-regulates HLA-DR expression in infected interferon gamma (IFN-gamma)-stimulated fibroblasts at 1 day after infection. Decreased HLA-DR expression was not observed on cells infected with an HCMV strain lacking the pp65 gene (RVAD65), but was observed on cells transfected with the pp65 gene. HLA-DR expression accumulated in vacuoles near the nucleus in HCMV-infected, but not in uninfected or RVAD65-infected cells. In addition, the HLA-DR alpha-chain, but not the beta-chain or HLA-DM, was degraded in HCMV-infected but not in RVAD65-infected cells. Thus, the HCMV protein pp65 mediates decreased expression of HLA-DR, by mediating an accumulation of HLA class II molecules in lysosomes that results in degradation of the HLA-DR alpha-chain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport
  • Cytomegalovirus / chemistry
  • Cytomegalovirus / genetics
  • Cytomegalovirus / immunology*
  • Dendritic Cells / immunology
  • Fibroblasts / ultrastructure
  • Fibroblasts / virology
  • Flow Cytometry
  • Gene Deletion
  • Gene Expression
  • HLA-D Antigens / metabolism
  • HLA-DR Antigens / genetics
  • HLA-DR Antigens / metabolism*
  • Humans
  • Interferon-Stimulated Gene Factor 3
  • Interferon-gamma / pharmacology
  • Janus Kinase 1
  • Janus Kinase 2
  • Leukocytes, Mononuclear / immunology
  • Lysosomes / metabolism*
  • Microscopy, Confocal
  • Phosphoproteins / genetics
  • Phosphoproteins / physiology*
  • Protein-Tyrosine Kinases / metabolism
  • Proto-Oncogene Proteins*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction
  • Transcription Factors / metabolism
  • Transfection
  • Viral Matrix Proteins / genetics
  • Viral Matrix Proteins / physiology*

Substances

  • HLA-D Antigens
  • HLA-DM antigens
  • HLA-DR Antigens
  • Interferon-Stimulated Gene Factor 3
  • Phosphoproteins
  • Proto-Oncogene Proteins
  • Transcription Factors
  • Viral Matrix Proteins
  • cytomegalovirus matrix protein 65kDa
  • gamma interferon activation factor
  • Interferon-gamma
  • Protein-Tyrosine Kinases
  • JAK1 protein, human
  • JAK2 protein, human
  • Janus Kinase 1
  • Janus Kinase 2