CD20-Specific Immunoligands Engaging NKG2D Enhance gamma delta T Cell-Mediated Lysis of Lymphoma Cells

摘要

Human gamma delta T cells are innate-like T cells which are able to kill a broad range of tumour cells and thus may have potential for cancer immunotherapy. The activating receptor natural killer group 2 member D (NKG2D) plays a key role in regulating immune responses driven by gamma delta T cells. Here, we explored whether recombinant immunoligands consisting of a CD20 single-chain fragment variable (scFv) linked to a NKG2D ligand, either MHC class I chain-related protein A (MICA) or UL16 binding protein 2 (ULBP2), could be employed to engage gamma delta T cells for tumour cell killing. The two immunoligands, designated MICA: 7D8 and ULBP2: 7D8, respectively, enhanced cytotoxicity of ex vivo-expanded gamma delta T cells against CD20-positive lymphoma cells. Both V delta 1 and V delta 2 gamma delta T cells were triggered by MICA: 7D8 or ULBP2: 7D8. Killing of CD20-negative tumour cells was not induced by the immunoligands, indicating their antigen specificity. MICA: 7D8 and ULBP2: 7D8 acted in a dose-dependent manner and induced cytotoxicity at nanomolar concentrations. Importantly, chronic lymphocytic leukaemia (CLL) cells isolated from patients were sensitized by the two immunoligands for gamma delta T cell cytotoxicity. In a combination approach, the immunoligands were combined with bromohydrin pyrophosphate (BrHPP), an agonist for Vd2 gamma delta T cells, which further enhanced the efficacy in target cell killing. Thus, employing tumour-directed recombinant immunoligands which engage NKG2D may represent an attractive strategy to enhance antitumour cytotoxicity of gamma delta T cells.