Direct visualization of the dynamics of antigen presentation in human cells infected with cytomegalovirus revealed by antibodies mimicking TCR specificity

Eur J Immunol. 2010 Jun;40(6):1552-65. doi: 10.1002/eji.200939875.

Abstract

There are no direct means to study class I MHC presentation in human normal or diseased cells. Using CMV-infected human cells and applying novel mAb that mimic T-cell receptor specificity directed toward the immunogenic epitope of the viral pp65 protein presented on HLA-A2 molecules, we directly imaged the dynamics of Ag presentation in infected cells. We demonstrate that following infection large intracellular pools of HLA-A2/pp65 complexes are localized to the Golgi. These HLA-A2/pp65 pools account for the majority of total HLA-A2 molecules in infected cells. Interestingly, these large pools are sequestered inside infected cells and only a small portion of them are exported to the cell surface. Virus-induced class I MHC down-regulation did not affect the intracellular pool of HLA-A2/pp65 complexes. Our data also suggest that proteasome function influences the release of class I complexes to the membrane. We present herein a new and direct molecular tool to study the dynamics of viral Ag presentation that may further elucidate the balance between immune response versus viral escape.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal*
  • Antibodies, Viral / immunology
  • Antigen Presentation / immunology*
  • Cell Separation
  • Cytomegalovirus Infections / immunology*
  • Cytomegalovirus Infections / metabolism
  • Electrophoresis, Polyacrylamide Gel
  • Flow Cytometry
  • HLA-A2 Antigen / immunology*
  • HLA-A2 Antigen / metabolism
  • Humans
  • Microscopy, Confocal
  • Molecular Mimicry
  • Phosphoproteins / immunology*
  • Phosphoproteins / metabolism
  • Receptors, Antigen, T-Cell / immunology
  • Receptors, Antigen, T-Cell / metabolism
  • T-Cell Antigen Receptor Specificity / immunology
  • Viral Matrix Proteins / immunology*
  • Viral Matrix Proteins / metabolism

Substances

  • Antibodies, Monoclonal
  • Antibodies, Viral
  • HLA-A2 Antigen
  • Phosphoproteins
  • Receptors, Antigen, T-Cell
  • Viral Matrix Proteins
  • cytomegalovirus matrix protein 65kDa