研究概要
次要终点为评估安全性和有效性,以及评估免疫动力学。
中文摘要
恒定自然杀伤T(iNKT)细胞具有细胞毒活性和免疫调节功能,在癌症免疫治疗中受到关注。我们开展了一项1期首次人体临床试验,评估由诱导多能干细胞生成的临床级同种异体iNKT细胞(iPSC-iNKT细胞)在复发性头颈癌患者中的安全性和疗效(jRCT2033200116)。主要终点是剂量限制性毒性(DLT)的发生率。次要终点是评估安全性和疗效,以及评估免疫动力学。iPSC-iNKT细胞经动脉给药于10例患者。1例受试者在第二次给药时出现3级皮疹,被确定为DLT。未在任何患者中观察到其他严重不良事件。2例患者的肿瘤进展受到抑制,在这些患者中观察到记忆表型和效应表型CD8+ T细胞的克隆扩增,同时伴有IFN-γ信号通路的激活。在此,我们表明iPSC-iNKT细胞是安全的,并具有作为实体瘤免疫治疗的治疗潜力。
展开英文摘要原文
Invariant Natural killer T (iNKT) cells exhibit cytotoxic activity and immunomodulatory functions and have gained interest in cancer immunotherapy. We conducted a phase 1, first-in human clinical trial to evaluate the safety and efficacy of clinical-grade allogeneic iNKT cells generated from induced pluripotent stem cells (iPSC-iNKT cells) in patients with recurrent head and neck cancer (jRCT2033200116). The primary endpoint was the incidence of dose-limiting toxicity (DLT). The secondary endpoints were to assess safety and efficacy, as well as to evaluate immunological dynamics. iPSC-iNKT cells were administered intra-arterially to 10 patients. One subject developed grade 3 skin rash at the second dose, identified as DLT. No other severe adverse events were observed in any patients. Tumor progression was suppressed in two patients, in whom clonal expansion of memory- and effector-phenotype CD8 + T cells was observed, along with activation of the IFN-γ signaling pathway. Here, we show that iPSC-iNKT cells are safe and possess therapeutic potential as an immunotherapy for solid tumors.
论文信息
- 作者
- Iinuma T、Kurokawa T、Aoki T、Onodera A、Fukazawa T、Yamada D、Kitahara G、Okoshi M
- 第一作者单位
- Department of Otorhinolaryngology, Head and Neck Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.Japan
- 通讯作者单位
- Department of Medical Immunology, Graduate School of Medicine, Chiba University, Chiba, Japan. motohashi@faculty.chiba-u.jp.Japan
- 文献类型
- I 期临床试验 · 非美国政府资助研究
- 期刊
- Nature communications2025 Nov 26