研究概要
这些结果证明了 CYT-303 有潜力成为针对 HCC 的安全有效疗法。
中文摘要
Glypican-3(GPC3)是一种胚胎性肿瘤抗原,在肝细胞癌等多种实体瘤中高表达,而成人正常组织中几乎不表达(胎盘除外)。NKp46激活受体表达于所有NK细胞,包括肿瘤浸润NK细胞。FLEX-NK是一种制备四价多功能NK细胞衔接抗体的平台。CYT-303基于FLEX-NK构建,含新型人源化NKp46结合结构域(不诱导NKp46内化)及靶向GPC3近膜结构域的人源化结合结构域,可重定向NK细胞杀伤肝癌。CYT-303对GPC3和NKp46均具有亚纳摩尔级亲和力,能高效介导NK细胞杀伤多种肝癌细胞系和肿瘤球。更值得注意的是,它可逆转NK细胞经多轮连续肿瘤杀伤后产生的功能障碍;还能介导GPC3阳性肝癌的抗体依赖性细胞吞噬和补体依赖性细胞毒作用。食蟹猴每周静脉给药、连续28天、剂量最高60 mg/kg,未出现毒性或细胞因子释放。结果显示CYT-303可能成为安全有效的肝细胞癌治疗方法。
展开英文摘要原文
Glypican-3 (GPC3) is an oncofetal antigen that is highly expressed in multiple solid tumors, including hepatocellular carcinoma, and is barely expressed in adult normal tissues except the placenta. NKp46 activation receptor is expressed in all-natural killer (NK) cells, including tumor-infiltrating NK cells. FLEX-NK TM is a platform for the production of tetravalent multifunctional antibody NK cell engagers (NKE). CYT-303 was designed using the FLEX-NK scaffold, incorporating a novel humanized NKp46 binder that does not induce NKp46 internalization and a humanized GPC3 binder that targets the membrane-proximal lobe to mediate NK cell-redirected killing of HCC tumors. CYT-303 shows sub-nanomolar binding affinities to both GPC3 and NKp46. CYT-303 was highly potent and effective in mediating NK cell-redirected cytotoxicity against multiple HCC tumor cell lines and tumor spheroids. More interestingly, it can reverse the dysfunction induced in NK cells following repeated rounds of serial killing of tumors. It also mediated antibody-dependent cellular phagocytosis (ADCP) and complement-dependent cytotoxicity against GPC3-expressing HCC tumors. In vivo, CYT-303 showed no toxicity or cytokine release in cynomolgus monkeys up to the highest dose (60 mg/kg), administered weekly by intravenous infusion for 28 days. These results demonstrate the potential of CYT-303 to be a safe and effective therapy against HCC.
论文信息
- 作者
- Arulanandam A、Lin L、Chang HM、Cerutti M、Choblet S、Gao P、Rath A、Bensussan A
- 单位
- Cytovia Therapeutics, Inc., Natick, MA 01760, USA.United States
- 文献类型
- 非美国政府资助研究
- 期刊
- Cells2023 Mar 24