Monoclonal antibodies against the 4-1BB T-cell activation molecule eradicate established tumors

Author:  ["Ignacio Melero","Walter W. Shuford","Stephanie Ashe Newby","Alejandro Aruffo","Jeffrey A. Ledbetter","Karl Erik Hellström","Robert S. Mittler","Lieping Chen"]

Publication:  Nature Medicine

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Tags:     Medicine

Abstract

The 4-1BB glycoprotein is a member of the tumor necrosis factor receptor superfamily1–4 and binds to a high-affinity ligand (4-1BBL) expressed on several antigen-presenting cells such as macrophages and activated B cells5,6. Expression of 4-1BB is restricted to primed CD4+ and CD8+ T cells7, and 4-1BB signaling either by binding to 4-1BBL or by antibody ligation delivers a dual mitogenic signal for T-cell activation and growth8–12. 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.

Cite this article

Melero, I., Shuford, W., Newby, S. et al. Monoclonal antibodies against the 4-1BB T-cell activation molecule eradicate established tumors. Nat Med 3, 682–685 (1997). https://doi.org/10.1038/nm0697-682

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