BCR-ABL peptide vaccination in healthy subjects: immunological responses are equivalent to those in chronic myeloid leukaemia patients

Leuk Res. 2011 Mar;35(3):369-72. doi: 10.1016/j.leukres.2010.05.028. Epub 2010 Jun 22.

Abstract

We and others have reported that vaccination of chronic myeloid leukaemia (CML) patients with e14a2 BCR-ABL junctional peptides can elicit moderate but transient T cell responses. To determine whether CML patients may be tolerised to BCR-ABL, here we used the same schedule to vaccinate 5 healthy subjects. Although IFN-γ and granzyme-B production, and proliferative responses to the vaccine peptides were detected in all 5 cases, responses were statistically similar to CML patients. CML patients are therefore not appreciably tolerised to BCR-ABL, and junctional peptides may only be moderately immunogenic, underlining the importance of antigen immunogenicity when designing vaccination strategies.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cancer Vaccines / immunology*
  • Cancer Vaccines / therapeutic use
  • Case-Control Studies
  • Cell Proliferation
  • Enzyme-Linked Immunosorbent Assay
  • Fusion Proteins, bcr-abl / genetics
  • Fusion Proteins, bcr-abl / immunology*
  • Granzymes / metabolism
  • Humans
  • Interferon-gamma / metabolism
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics
  • Leukemia, Lymphocytic, Chronic, B-Cell / immunology*
  • Leukemia, Lymphocytic, Chronic, B-Cell / pathology*
  • Peptide Fragments / immunology*
  • Prognosis
  • T-Lymphocytes / immunology*

Substances

  • Cancer Vaccines
  • Peptide Fragments
  • Interferon-gamma
  • Fusion Proteins, bcr-abl
  • Granzymes