| Literature DB >> 31155232 |
Laurent Gauthier1, Ariane Morel2, Nadia Anceriz2, Benjamin Rossi2, Audrey Blanchard-Alvarez2, Gwendoline Grondin2, Sylvia Trichard2, Cédric Cesari2, Melody Sapet2, Frédéric Bosco2, Hélène Rispaud-Blanc2, Franceline Guillot2, Stéphanie Cornen2, Alain Roussel3, Béatrice Amigues3, Guillaume Habif2, Flavien Caraguel2, Sandrine Arrufat2, Romain Remark2, François Romagné4, Yannis Morel2, Emilie Narni-Mancinelli5, Eric Vivier6.
Abstract
Over the last decade, various new therapies have been developed to promote anti-tumor immunity. Despite interesting clinical results in hematological malignancies, the development of bispecific killer-cell-engager antibody formats directed against tumor cells and stimulating anti-tumor T cell immunity has proved challenging, mostly due to toxicity problems. We report here the generation of trifunctional natural killer (NK) cell engagers (NKCEs), targeting two activating receptors, NKp46 and CD16, on NK cells and a tumor antigen on cancer cells. Trifunctional NKCEs were more potent in vitro than clinical therapeutic antibodies targeting the same tumor antigen. They had similar in vivo pharmacokinetics to full IgG antibodies and no off-target effects and efficiently controlled tumor growth in mouse models of solid and invasive tumors. Trifunctional NKCEs thus constitute a new generation of molecules for fighting cancer. VIDEO ABSTRACT.Entities:
Keywords: cancer immunotherapy; monoclonal antibodies; natural killer cells
Year: 2019 PMID: 31155232 DOI: 10.1016/j.cell.2019.04.041
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582