Multifunctional Natural Killer Cell Engagers Targeting NKp46 Trigger Protective Tumor Immunity
Author(s) -
Laurent Gauthier,
Ariane Morel,
Nadia Anceriz,
Benjamín Rossi,
Audrey Blanchard-Alvarez,
Gwendoline Grondin,
Sylvia Trichard,
Cédric Cesari,
Melody Sapet,
Frédéric Bosco,
Hélène Rispaud-Blanc,
Franceline Guillot,
Stéphanie Cornen,
Alain Roussel,
Béatrice Amigues,
Guillaume Habif,
Flavien Caraguel,
Sandrine Arrufat,
Romain Remark,
François Romagné,
Yannis Morel,
Émilie Narni-Mancinelli,
Éric Vivier
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.04.041
Subject(s) - biology , cd16 , chimeric antigen receptor , antigen , antibody , immunity , immunology , natural killer cell , cancer research , immunotherapy , immune system , in vitro , cytotoxic t cell , cd8 , cd3 , biochemistry
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.
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