CD20
癌症研究
淋巴瘤
B细胞
T细胞
自然杀伤细胞
细胞
白细胞介素21
免疫学
生物
细胞毒性
医学
体外
免疫系统
抗体
遗传学
生物化学
作者
Olivier Demaria,Guillaume Habif,Marie Vétizou,Laurent Gauthier,Romain Remark,Laura Chiossone,Constance Vagne,Lucas Rebuffet,Rachel Courtois,Caroline Denis,François Le Floch,Marianna Müller,Mathilde Girard-Madoux,Séverine Augier,Julie Lopez,Barbara Carrette,Aurélie Maguer,Jean-Baptiste Vallier,Gwendoline Grondin,William Baron
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2024-11-15
卷期号:9 (101)
被引量:1
标识
DOI:10.1126/sciimmunol.adp3720
摘要
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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