Tumor-associated carbohydrate antigens: a possible avenue for cancer prevention

Immunol Cell Biol. 2005 Aug;83(4):440-8. doi: 10.1111/j.1440-1711.2005.01347.x.

Abstract

Here we examine the use of glycopeptides containing tumour-associated carbohydrate antigens (TACA) as potential preventive vaccines for carcinomas. Our recent results suggest that CD8+ T cells (CTL) are capable of recognizing TACA in a conventional class I MHC-restricted fashion. The ThomsenFriedenreich antigen (TF), a disaccharide, and Tn, its immediate precursor, are TACA largely expressed in carcinomas. TF and Tn can be successfully used as Th-independent vaccines when conjugated to designer peptides with optimal binding affinity for class I MHC molecules. TF- and Tn-specific CTL generated using this strategy are capable of recognizing TACA-expressing tumours in vitro, suggesting that glycopeptides are as effectively presented by class I MHC molecules as non-glycosylated peptides. Because the exact sequences of endogenously synthesized glycopeptides are unknown, the TACA-specific T cell repertoire elicited by carbohydrate-based vaccines is assumed to be degenerate. Here we report that mice genetically manipulated to develop TACA-expressing mammary tumours are not tolerant to glycopeptide vaccination. Moreover, we tested the immunogenicity of designer glycopeptides capable of binding multiple HLA alleles as a novel approach for the development of vaccines potentially useful for vaccination of a large fraction of the general population. Our results have suggested that CTL derived from normal donors respond with high efficiency to glycopeptides in vitro, opening a new avenue for the design of prospective vaccines for cancer prevention.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Animals
  • Antigens, Tumor-Associated, Carbohydrate / genetics
  • Antigens, Tumor-Associated, Carbohydrate / immunology*
  • Antigens, Tumor-Associated, Carbohydrate / metabolism
  • Cancer Vaccines / immunology
  • Female
  • Glycopeptides / immunology
  • Histocompatibility Antigens Class I / genetics
  • Histocompatibility Antigens Class I / immunology
  • Histocompatibility Antigens Class I / metabolism
  • Humans
  • Mice
  • Mice, Transgenic
  • Middle Aged
  • Mucin-1 / genetics
  • Mucin-1 / immunology
  • Mucin-1 / metabolism
  • Neoplasms / immunology*
  • Neoplasms / prevention & control*
  • Protein Binding
  • T-Lymphocytes, Cytotoxic / immunology
  • Vaccination

Substances

  • Antigens, Tumor-Associated, Carbohydrate
  • Cancer Vaccines
  • Glycopeptides
  • Histocompatibility Antigens Class I
  • Mucin-1
  • Thomsen-Friedenreich antigen