Humoral immune response against melanoma antigens induced by vaccination with cytokine gene-modified autologous tumor cells

Int J Cancer. 2004 Jan 10;108(2):307-13. doi: 10.1002/ijc.11537.

Abstract

Although the existence of a humoral response against tumor-associated antigens is well appreciated, a systematic analysis of its possible induction by the tumor remains missing. We compared the specific IgG response of Stage IV melanoma patients during vaccination. Patients had been treated within 2 clinical trials with autologous tumor cells gene-modified for IL-7 or IL-12. A panel of 27 tumor-associated antigens (HD-MM-01 to HD-MM-27) was isolated by a SEREX screening of a testis cDNA library using a pool of 5 sera from patients after vaccination. All antigens were retested with individual sera of 12 patients both pre- and post-vaccination. A serological response was induced during vaccination against 18 antigens. Remarkably, induction was detected only in patients included in the screening pool. The low overlap between sero-reactivity of the 12 patients suggested a very individualized immunological reaction. Two of 5 sera included in the screening pool exhibited a high frequency of induced humoral responses. The same patients had been shown to have a high Karnovsky index and had generated lytic cytotoxic T cells against the tumor. Besides 2 known cancer-germline genes (SCP-1 and PLU-1), the other isolated antigens were expressed in a non-tumor-specific fashion as analyzed by virtual Northern blot or RT-PCR. The properties of homologues to several of the identified tumor-antigens, especially PLU-1, SCP-1, DNEL2, CLOCK, and PIASx-alpha, suggest further investigation of their possible function in malignant melanoma. We conclude that a strong humoral response against tumor-associated antigens is inducible by tumor cells and that this response is very individual.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Neoplasm / blood*
  • Antigens, Neoplasm / immunology*
  • Cancer Vaccines / therapeutic use*
  • Cloning, Molecular
  • Cytotoxicity, Immunologic
  • DNA Primers / chemistry
  • Gene Library
  • Genetic Therapy
  • Humans
  • Immunotherapy
  • Interleukin-12 / genetics
  • Interleukin-7 / genetics
  • Interleukins / genetics*
  • Male
  • Melanoma / immunology*
  • Melanoma / therapy
  • Reverse Transcriptase Polymerase Chain Reaction
  • Skin Neoplasms / immunology*
  • Skin Neoplasms / therapy
  • Testis / metabolism
  • Vaccination

Substances

  • Antibodies, Neoplasm
  • Antigens, Neoplasm
  • Cancer Vaccines
  • DNA Primers
  • Interleukin-7
  • Interleukins
  • Interleukin-12