| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10900120 | Cancer Letters | 2008 | 7 Pages | 
Abstract
												huHMFG-1 (AS1402) is a humanised IgG1 against MUC1, which exerts tumour cell killing through antibody-dependent cellular cytotoxicity (ADCC) mediated by natural killer (NK) cells. Here, we explored the capacity of invariant NKT (iNKT) cells, which are known to activate NK cells, and toll-like receptor (TLR) ligands which activate both iNKT and NK cells, to enhance huHMFG-1-ADCC. Addition of iNKT cells, as well as TLR2/6, 7, 8 and 9 agonists to PBMC improved the efficacy of huHMFG-1. These results suggest that transfer of ex vivo expanded iNKT cells or TLR agonist treatment may improve the efficacy of NK cell-mediated antibody-based tumour immunotherapies.
											Keywords
												
											Related Topics
												
													Life Sciences
													Biochemistry, Genetics and Molecular Biology
													Cancer Research
												
											Authors
												MarÃa Moreno, Berber M. Mol, Silvia von Mensdorff-Pouilly, René H.M. Verheijen, B.Mary E. von Blomberg, Alfons J.M. van den Eertwegh, Rik J. Scheper, Hetty J. Bontkes, 
											