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The 4-1BB glycoprotein is a member of the tumor necrosis factor receptor superfamily and binds to a high-affinity ligand (4-1BBL) expressed on several antigen-presenting cells such as macrophages and activated B cells. Expression of 4-1BB is restricted to primed CD4+ and CD8+ T cells, and 4-1BB signaling either by binding to 4-1BBL or by antibody ligation delivers a dual mitogenic signal for T-cell activation and growth. These observations suggest an important role for 4-1BB in the amplification of T cell-mediated immune responses. We now show that administration of anti-4-1BB monoclonal antibodies can eradicate established large tumors in mice, including the poorly immunogenic Ag104A sarcoma and the highly tumorigenic P815 masto cytoma. The immune response induced by anti-4- 1BB monoclonal antibodies is mediated by both CD8+ and CD4+ T cells and is accompanied by a marked augmentation of tumor-selective cytolytic T-cell activity. Our data suggest that a similar approach may be efficacious for immunotherapy of human cancer.

Original publication

DOI

10.1038/nm0697-682

Type

Journal article

Journal

Nature medicine

Publication Date

06/1997

Volume

3

Pages

682 - 685

Addresses

Bristol-Myers Squibb Pharmaceutical Research Institute, Seattle, Washington 98121, USA.

Keywords

CD4-Positive T-Lymphocytes, CD8-Positive T-Lymphocytes, T-Lymphocytes, Cytotoxic, Tumor Cells, Cultured, Animals, Mice, Inbred C3H, Mice, Inbred DBA, Mice, Mast-Cell Sarcoma, Sarcoma, Experimental, Receptors, Tumor Necrosis Factor, Receptors, Nerve Growth Factor, Antigens, CD, Antibodies, Monoclonal, Neoplasm Transplantation, Female, Tumor Necrosis Factor Receptor Superfamily, Member 9