B7-1, IFN gamma and anti-CTLA-4 co-operate to prevent T-cell tolerization during immunotherapy against a murine T-lymphoma

Int J Cancer. 2000 Aug 15;87(4):539-47.

Abstract

We previously reported on a murine T lymphoma cell line, BW-Sp3, with inherent immunogenicity. BW-Sp3 tumors can elicit an anti-tumor CD8(+) CTL response capable of mediating a regression of subcutaneous tumors. However, this immune response is inadequate to eliminate cancer cells completely in a significant percentage of the recipients, resulting in progressing tumors. In this tumor model, tumor progression correlated with a tolerization of tumor-reactive T cells and cellular immunotherapy of tumor bearing animals, with or without B7-mediated costimulation, even increased tumor progression (Raes et al, 1998). In the present study, we investigated whether the co-expression of IFN gamma, together with B7-1, could have beneficial effects on immunotherapy. Although immunotherapy with IFN gamma and B7-1 single transfectants tended to tolerize anti-tumor T-cells and consequently increased tumor growth, the B7-1/IFN gamma double transfectants resulted in a more beneficial outcome. This phenomenon correlated with an increased CTL-inducing potential of the double transfectants. Secondly, we wondered whether CTLA-4 signalling was involved in the down-regulation of the anti-tumor response. Indeed, when immunotherapy was provided along with anti-CTLA-4, the protection by B71/IFN gamma double transfectants was further improved and the tumor-promoting effect of BW-Sp3(B7-1) was compensated for. Our results indicate that B7-1, IFN gamma and the blockade of CTLA-4 cooperate to tilt the balance in favour of tumor elimination, while either factor alone fails to do so or even promotes tumor growth.

MeSH terms

  • Abatacept
  • Animals
  • Antibodies, Monoclonal / immunology*
  • Antigens, CD
  • Antigens, Differentiation / immunology*
  • Antigens, Differentiation / physiology
  • B7-1 Antigen / genetics
  • B7-1 Antigen / immunology*
  • CTLA-4 Antigen
  • Cancer Vaccines / genetics
  • Cancer Vaccines / immunology
  • Female
  • Immune Tolerance / immunology
  • Immunoconjugates*
  • Immunotherapy, Active / methods*
  • Interferon-gamma / genetics
  • Interferon-gamma / immunology*
  • Lymphoma, T-Cell / immunology*
  • Lymphoma, T-Cell / therapy
  • Mice
  • Mice, Inbred AKR
  • Neoplasm Transplantation
  • Signal Transduction / physiology
  • T-Lymphocytes, Cytotoxic / immunology*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • Antigens, Differentiation
  • B7-1 Antigen
  • CTLA-4 Antigen
  • Cancer Vaccines
  • Ctla4 protein, mouse
  • Immunoconjugates
  • Abatacept
  • Interferon-gamma