Elevated expression of ICAM1 (CD54) and minimal expression of LFA3 (CD58) in Epstein-Barr-virus-positive nasopharyngeal carcinoma cells

Int J Cancer. 1992 Apr 1;50(6):863-7. doi: 10.1002/ijc.2910500605.

Abstract

Undifferentiated nasopharyngeal carcinoma (NPC) is a remarkable entity among human tumors because of its constant association with the Epstein-Barr virus (EBV). Malignant epithelial cells harbor the EBV genome and often express at least 2 species of latent EBV protein (EBNA1 and LMP1). Despite the massive presence of tumor-infiltrating lymphocytes, NPC cells obviously escape immune surveillance directed to EBV antigens. Previous investigations carried out on EBV-positive Burkitt lymphoma (BL) cells have shown that this fact may be partially accounted for by a lack of expression of ICAM1 (CD54) and LFA3 (CD58). ICAM1 and LFA3 have therefore been investigated in fresh NPC biopsies and transplanted NPCs. With only 1 exception out of 9 cases, NPC cells appear to express high levels of ICAM1 and low levels of LFA3. This is a complete inversion of the pattern observed in normal epithelial cells in vivo. Additional investigations will be required to determine to what extent these characteristics affect T-cell interactions with NPC cells, specially in the process of EBV-antigen recognition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal
  • Antigens, CD / analysis*
  • Antigens, Surface / analysis*
  • CD58 Antigens
  • Cell Adhesion Molecules / analysis*
  • Cell Adhesion Molecules / genetics
  • Cell Line
  • Herpesvirus 4, Human / genetics
  • Herpesvirus 4, Human / isolation & purification*
  • Histocompatibility Antigens Class I / analysis
  • Humans
  • Intercellular Adhesion Molecule-1
  • Membrane Glycoproteins / analysis*
  • Mice
  • Mice, Nude
  • Nasopharyngeal Neoplasms / immunology
  • Nasopharyngeal Neoplasms / microbiology*
  • Nasopharyngeal Neoplasms / pathology*
  • Nasopharyngeal Neoplasms / surgery
  • Neoplasm Transplantation
  • Receptors, Virus / analysis*
  • Transcription, Genetic
  • Transplantation, Heterologous
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • Antigens, Surface
  • CD58 Antigens
  • Cell Adhesion Molecules
  • Histocompatibility Antigens Class I
  • Membrane Glycoproteins
  • Receptors, Virus
  • Intercellular Adhesion Molecule-1