医学
皮疹
不利影响
细胞毒性T细胞
免疫疗法
临床试验
癌症研究
免疫学
毒性
临床终点
干细胞
头颈部癌
临床研究阶段
诱导多能干细胞
癌症免疫疗法
黑色素瘤
肿瘤科
自然杀伤性T细胞
癌症
内科学
细胞疗法
免疫系统
恶性转化
恶性细胞
癌细胞
作者
Tomohisa Iinuma,Tomoya Kurokawa,Takahiro Aoki,Atsushi Onodera,Tominaga Fukazawa,Daisuke Yamada,Genta Kitahara,Momoko Okoshi,M Yamaguchi,Hiroko Okura,Satoko Sasaki,Yoshie Sasako,Sachiko Kira,Jafar Sharif,Yukio Tsuchiyama,Midori Kobayashi,Norihiko Kobayashi,Takuro Horikoshi,Yosuke Inaba,Hideki Hanaoka
标识
DOI:10.1038/s41467-025-66801-w
摘要
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.
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