Toll-like Receptors 3 and 7 Agonists Enhance Tumor Cell Lysis by Human gamma delta T Cells

作者：Shojaei Harried; Oberg Hans Heinrich; Juricke Matthias; Marischen Lothar; Kunz Monika; Mundhenke Christoph; Gieseler Frank; Kabelitz Dieter; Wesch Daniela^*

来源：Cancer Research, 2009, 69(22): 8710-8717.

DOI：10.1158/0008-5472.CAN-09-1602

Toll-like receptor (TLR) agonists are considered adjuvants in clinical trials of cancer immunotherapy. Here, we investigated the modulation of gamma delta T cell-mediated tumor cell lysts by TLR ligands. gamma delta T-cell cytotoxicity and granzyme A/B production were enhanced after pretreatment of tumor cells with TLR3 [poly(I:C)] or TLR7 ligand (imiquimod). We examined TLR3- and TLR7-expressing pancreatic adenocarcinomas, squamous cell carcinomas of head and neck and lung carcinomas. Poly(I:C) treatment of pancreatic adenocarcinomas followed by coculture with gamma delta T cells resulted in an upregulation of CD54 on the tumor cells. The interaction of CD54 and the corresponding ligand CD11a/CD18 expressed on gamma delta T cells is responsible for triggering effector function in gamma delta T cells. Moreover, treatment with imiquimod downregulated MHC class I molecules on tumor cells possibly resulting in a reduced binding affinity for inhibitory receptor NKG2A expressed on gamma delta T cells. These results indicate that TLR3 or TLR7 ligand stimulation of tumor cells enhances the cytotoxic activity of expanded gamma delta T cells of cancer patients in vitro. [Cancer Res 2009;69(22):8710-7]

• 出版日期2009-11-15