Bortezomib improves adoptive T cell therapy by sensitizing cancer cells to FasL cytotoxicity

Cancer immunotherapy shows great promise but many patients fail to show objective responses, including in cancers that can respond well such as melanoma and renal adenocarcinoma. The proteasome inhibitor bortezomib sensitizes solid tumors to apoptosis in response to TNF-family death ligands.

Since T cells provide multiple death ligands at the tumor site, we investigated the effects of bortezomib on T cell responses in immunotherapy models involving low-avidity antigens. Bortezomib did not affect lymphocyte or tissue-resident CD11c+CD8+ dendritic cell counts in tumor-bearing mice, did not inhibit dendritic cell expression of co-stimulatory molecules and did not decrease MHC class I/II-associated antigen presentation to cognate T cells. Rather, bortezomib activated NF-κB p65 in CD8+ T cells, stabilizing expression of T cell receptor CD3ζ and IL-2 receptor-α, while maintaining IFN-γ secretion to improve FasL-mediated tumor lysis. Notably, bortezomib increased tumor cell surface expression of Fas in mice as well as human melanoma tissue from a responsive patient. In renal tumor-bearing immunodeficient Rag2-/- mice, bortezomib treatment after adoptive T cell immunotherapy reduced lung metastases and enhanced host survival. Our findings highlight the potential of proteasome inhibitors to enhance antitumor T cell function in the context of cancer immunotherapy.

Cancer research. 2015 Oct 22 [Epub ahead of print]

Anil Shanker, Samuel T Pellom, Duafalia F Dudimah, Menaka C Thounaojam, Rachel L de Kluyver, Alan D Brooks, Hideo Yagita, Daniel W McVicar, William J Murphy, Dan L Longo, Thomas J Sayers

Biochemistry and Cancer Biology, Meharry Medical College/ Vanderbilt-Ingram Cancer Center, Biochemistry and Cancer Biology, Meharry Medical College/ Vanderbilt-Ingram Cancer Center. , Biochemistry and Cancer Biology, Meharry Medical College/ Vanderbilt-Ingram Cancer Center. , Biochemistry and Cancer Biology, Meharry Medical College. , Cancer and Inflammation Program, National Cancer Institute. , Cancer and Inflammation Program, SAIC-Frederick, Inc. , National Cancer Institute - Frederick. , Department of Immunology, Juntendo University School of Medicine. , Cancer and Inflammation Program, National Cancer Institute. , Dermatology & Internal Medicine, School of Medicine, University of California, Davis. , Laboratory of Molecular Biology and Immunology, Biomedical Research Center, National Institute on Aging. , CIP, NCI.

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