Immunological monitoring of cancer vaccine therapy

Expert Opin Biol Ther. 2004 Oct;4(10):1677-84. doi: 10.1517/14712598.4.10.1677.

Abstract

Immunological treatment of malignant diseases in humans aiming at the induction and proliferation of antigen-specific T cells has made rapid progress in recent years. A growing number of tumour-associated antigens, potentially synergistic combinations with adjuvants, and various routes of application provide new opportunities for cancer vaccination. Therefore, a highly accurate assessment of vaccine-induced T cell responses is required. Three T cell assays (tetramers, intracellular cytokine flow cytometry and ELISPOT assay) have emerged as first-line methods for monitoring T cell induction during vaccination. These assays are relatively easy to perform, reliable, sensitive and allow an ex vivo T cell analysis at the single cell level. Although at this stage assays are not a defined surrogate marker for clinical efficacy, they already provide information concerning the immunological potency of a given vaccine. In particular, comparing immune responses under various treatment conditions will help to develop more clinically efficient tumour vaccination. Novel assays, such as CD107 staining, human leukocyte antigen/green fluorescent protein-antigen-presenting cells or microarrays, and assays determining functions, such as proliferation assays, are beginning to complement first-line monitoring assays.

Publication types

  • Review

MeSH terms

  • Antigen-Antibody Reactions
  • Antigens, Neoplasm / immunology
  • Biopolymers
  • Biotinylation
  • Cancer Vaccines / immunology
  • Cancer Vaccines / therapeutic use*
  • Clinical Trials as Topic
  • Cytokines / metabolism
  • Cytotoxicity Tests, Immunologic
  • Enzyme-Linked Immunosorbent Assay
  • Flow Cytometry
  • Fluorescent Dyes / analysis
  • HLA Antigens / chemistry
  • HLA Antigens / immunology
  • Humans
  • Immunity, Cellular
  • Immunologic Tests*
  • Immunotherapy, Active*
  • Lymphocyte Activation
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Streptavidin / analysis
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Antigens, Neoplasm
  • Biopolymers
  • Cancer Vaccines
  • Cytokines
  • Fluorescent Dyes
  • HLA Antigens
  • Streptavidin