Enhancement of antitumor immunity by CTLA-4 blockade

Science. 1996 Mar 22;271(5256):1734-6. doi: 10.1126/science.271.5256.1734.

Abstract

One reason for the poor immunogenicity of many tumors may be that they cannot provide signals for CD28-mediated costimulation necessary to fully activate T cells. It has recently become apparent that CTLA-4, a second counterreceptor for the B7 family of costimulatory molecules, is a negative regulator of T cell activation. Here, in vivo administration of antibodies to CTLA-4 resulted in the rejection of tumors, including preestablished tumors. Furthermore, this rejection resulted in immunity to a secondary exposure to tumor cells. These results suggest that blockade of the inhibitory effects of CTLA-4 can allow for, and potentiate, effective immune responses against tumor cells.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abatacept
  • Animals
  • Antibodies / immunology
  • Antigens, CD
  • Antigens, Differentiation / immunology*
  • B7-1 Antigen / immunology
  • CD28 Antigens / immunology
  • CTLA-4 Antigen
  • Female
  • Graft Rejection
  • Immunoconjugates*
  • Immunologic Memory
  • Lymphocyte Activation*
  • Mice
  • Mice, Inbred A
  • Mice, Inbred BALB C
  • Neoplasm Transplantation
  • Neoplasms, Experimental / immunology*
  • T-Lymphocytes / immunology*
  • Transfection
  • Tumor Cells, Cultured

Substances

  • Antibodies
  • Antigens, CD
  • Antigens, Differentiation
  • B7-1 Antigen
  • CD28 Antigens
  • CTLA-4 Antigen
  • Ctla4 protein, mouse
  • Immunoconjugates
  • Abatacept