Tumor-reactive CD8+ T-cell responses after vaccination with NY-ESO-1 peptide, CpG 7909 and Montanide ISA-51: association with survival

Int J Cancer. 2010 Feb 15;126(4):909-18. doi: 10.1002/ijc.24850.

Abstract

Peptide-based vaccines have led to the induction of antigen-specific CD8(+) T-cell responses in patients with NY-ESO-1 positive cancers. However, vaccine-induced T-cell responses did not generally correlate with improved survival. Therefore, we tested whether a synthetic CpG 7909 ODN (deoxycytidyl-deoxyguanosin oligodeoxy-nucleotides) mixed with NY-ESO-1 peptide p157-165 and incomplete Freund's adjuvants (Montanide(R) ISA-51) led to enhanced NY-ESO-1 antigen-specific CD8(+) immune responses in patients with NY-ESO-1 or LAGE-1 expressing tumors. Of 14 HLA-A2+ patients enrolled in the study, 5 patients withdrew prematurely because of progressive disease and 9 patients completed 1 cycle of immunization. Nine of 14 patients developed measurable and sustained antigen-specific CD8(+) T-cell responses: Four had detectable CD8+ T-cells against NY-ESO-1 after only 2 vaccinations, whereas 5 patients showed a late-onset but durable induction of NY-ESO-1 p157-165 specific T-cell response during continued vaccination after 4 months. In 6 patients, vaccine-induced antigen-specific T-cells became detectable ex vivo and reached frequencies of up to 0.16 % of all circulating CD8(+) T-cells. Postvaccine T-cell clones were shown to recognize and lyse NY-ESO-1 expressing tumor cell lines in vitro. In 6 of 9 patients developing NY-ESO-1-specific immune responses, a favorable clinical outcome with overall survival times of 43+, 42+, 42+, 39+, 36+ and 27+ months, respectively, was observed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Neoplasm / therapeutic use*
  • Breast Neoplasms / immunology
  • Breast Neoplasms / pathology
  • CD8-Positive T-Lymphocytes / immunology*
  • Cancer Vaccines / therapeutic use*
  • Cell Line, Tumor
  • Female
  • Flow Cytometry
  • Humans
  • Immunotherapy / methods
  • Mannitol / analogs & derivatives*
  • Mannitol / therapeutic use
  • Melanoma / immunology
  • Membrane Proteins / therapeutic use*
  • Neoplasm Staging
  • Neoplasms / immunology*
  • Oleic Acids / therapeutic use*
  • Oligodeoxyribonucleotides / therapeutic use*
  • Ovarian Neoplasms / immunology
  • Ovarian Neoplasms / pathology
  • Sarcoma / immunology
  • Sarcoma / pathology
  • Vaccination / methods*

Substances

  • Antigens, Neoplasm
  • CTAG1B protein, human
  • Cancer Vaccines
  • Membrane Proteins
  • Oleic Acids
  • Oligodeoxyribonucleotides
  • ProMune
  • montanide ISA 51
  • Mannitol