HLA class I expression on human cancer cells. Implications for effective immunotherapy

Hum Immunol. 2000 Feb;61(2):158-65. doi: 10.1016/s0198-8859(99)00150-0.

Abstract

Early studies demonstrated the role of cytotoxic T cells as an immune defence mechanism against tumour cells. The demonstration of tumour antigen peptides and their presentation to T cells on major histocompatibility complex class I molecules highlighted the importance of these molecules in effective anti-tumour responses. It is well established that many tumours escape T cell recognition by loss or down regulation of class I molecule expression on the cell surface of tumour cells. Tumours which have lost class I expression are immunoselected and as a result have a propensity for growth and metastatic spread. With the development of cancer vaccine strategies for clinical use, there will be a future role for histocompatibility laboratories in determining class I expression on tumour cells in individual patients. These studies of expression will require not just the demonstration of total class I expression but the demonstration of locus and allele specific class I molecules involved in the relevant tumour peptide presentation. These studies will be pivotal in tailoring individual patient therapies. The identification of appropriate monoclonal antibody reagents for class I expression and techniques used on different kinds of tissue sections will be a component of the forthcoming 13th International Histocompatibility Workshop.

Publication types

  • Review

MeSH terms

  • Animals
  • Antigen Presentation
  • Antigens, Neoplasm / immunology
  • Cancer Vaccines / immunology*
  • HLA Antigens / metabolism*
  • Histocompatibility Antigens Class I / analysis
  • Histocompatibility Antigens Class I / immunology*
  • Humans
  • Immunotherapy
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • T-Lymphocytes / immunology
  • Vaccines, DNA

Substances

  • Antigens, Neoplasm
  • Cancer Vaccines
  • HLA Antigens
  • Histocompatibility Antigens Class I
  • Vaccines, DNA