A tetraspecific engager armed with a non-alpha IL-2 variant harnesses natural killer cells against B cell non-Hodgkin lymphoma

Olivier Demaria(Innate Pharma (France)), Guillaume Habif(Innate Pharma (France)), Marie Vétizou(Innate Pharma (France)), Laurent Gauthier(Innate Pharma (France)), Romain Remark(Innate Pharma (France)), Laura Chiossone(Innate Pharma (France)), Constance Vagne(Innate Pharma (France)), Lucas Rebuffet(Centre National de la Recherche Scientifique), Rachel Courtois(Innate Pharma (France)), Caroline Denis(Innate Pharma (France)), François Le Floch(Innate Pharma (France)), Marianna Müller(Innate Pharma (France)), Mathilde Girard-Madoux(Innate Pharma (France)), Séverine Augier(Innate Pharma (France)), Julie Lopez(Innate Pharma (France)), Barbara Carrette(Innate Pharma (France)), Aurélie Maguer(Innate Pharma (France)), Jean-Baptiste Vallier(Innate Pharma (France)), Gwendoline Grondin(Innate Pharma (France)), William Baron(Innate Pharma (France)), Justine Galluso(Innate Pharma (France)), Nadia Yessaad(Innate Pharma (France)), Marilyn Giordano(Innate Pharma (France)), Léa Simon(Innate Pharma (France)), Fabien Chanuc(Innate Pharma (France)), Audrey Blanchard Alvarez(Innate Pharma (France)), Ivan Perrot(Innate Pharma (France)), Cécile Bonnafous(Innate Pharma (France)), Agnès Représa(Innate Pharma (France)), Benjamín Rossi(Innate Pharma (France)), Ariane Morel(Innate Pharma (France)), Yannis Morel(Innate Pharma (France)), Carine Paturel(Innate Pharma (France)), Éric Vivier(Centre National de la Recherche Scientifique)
Science Immunology
November 15, 2024
Cited by 17

Abstract

NK cells offer a promising alternative to T cell therapies in cancer. We evaluated IPH6501, a clinical-stage, tetraspecific NK cell engager (NKCE) armed with a non-alpha IL-2 variant (IL-2v), which targets CD20 and was developed for treating B cell non-Hodgkin lymphoma (B-NHL). CD20-NKCE-IL2v boosts NK cell proliferation and cytotoxicity, showing activity against a range of B-NHL cell lines, including those with low CD20 density. Whereas it presented reduced toxicities compared with those commonly associated with T cell therapies, CD20-NKCE-IL2v showed greater killing efficacy over a T cell engager targeting CD20 in in vitro preclinical models. CD20-NKCE-IL2v also increased the cell surface expression of NK cell-activating receptors, leading to activity against CD20-negative tumor cells. In vivo studies in nonhuman primates and tumor mouse models further validated its efficacy and revealed that CD20-NKCE-IL2v induces peripheral NK cell homing at the tumor site. CD20-NKCE-IL2v emerges as a potential alternative in the treatment landscape of B-NHL.


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