Selective Inhibition of T Cell Tolerance as a Means of Enhancing Tumor Vaccines in a Mouse Model of Breast Cancer

Abstract

To determine if the addition of Go6976 to vaccine protocols will inhibit neu specific tolerance and enhance immunotherapy for breast cancer. Scope: In the Her-2/neu model of spontaneous breast cancer the immune system of these transgenic mice are tolerant to the neu protein. While immunity to neu can be demonstrated in the neu-transgenic mice (partial breaking of tolerance), this immunity is inadequate to prevent the spontaneous development of tumors and to prevent death from tumor challenge. Findings: By combining our regimen with a dose of cytoxan we can promote survival of tumor bearing mice when compared with no treatment, vaccine alone or vaccine + cytoxan. In particular, this combination is very effective in inhibiting tumor growth in the early period post-tumor challenge. Unfortunately, during the last year efforts to improve long term survival have not been successful. Significance: These data support the notion that the novel combination of PKC inhibitor + vaccine can enhance the efficacy of tumor vaccines. More work needs to be done to optimized the dosing schedule of this approach.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Jun 01, 2006
Accession Number
ADA460797

Entities

People

  • Jonathan Powell

Organizations

  • Johns Hopkins University

Tags

DTIC Thesaurus Topics

  • Biomedical Research
  • Breast Cancer
  • Cells
  • Department Of Defense
  • Diseases And Disorders
  • Immune System
  • Immune System Phenomena
  • Immunity
  • Immunomodulation
  • Immunotherapy
  • Inhibitors
  • Lymphatic System
  • Lymphocytes
  • Neoplasms
  • Survival
  • Therapy

Fields of Study

  • Biology

Readers

  • Immunology
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech