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TIL 治疗晚期子宫内膜癌的制备可行性与抗肿瘤活性

英文原题:Feasibility of Manufacturing and Antitumor Activity of TIL for Advanced Endometrial Cancers.

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Feasibility of Manufacturing and Antitumor Activity of TIL for Advanced Endometrial Cancers.

PubMed 2025/07/24(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

研究概要

这些发现证明了从 EC 肿瘤中体外扩增 TIL 的可行性。

中文摘要

Lifileucel 是一种获批用于晚期黑色素瘤的TIL(肿瘤浸润淋巴细胞)细胞疗法,也有望用于子宫内膜癌(EC)等其他实体瘤。本研究评估采用 Iovance 专有的 22 天 Gen2 制备流程从 EC 肿瘤制备 TIL 的可行性,并评估 TIL 产量、活率、免疫表型、TCR 克隆性和细胞毒活性等关键参数。11 份研究规模处理的 EC 肿瘤样本中,10 份(91%)成功产生超过 1 × 10⁹ 个活 TIL;中位产量为 1.1 × 10¹⁰ 个细胞,中位活率为 82.8%。4 份全规模处理的 EC 肿瘤样本均达到预设的总活细胞(TVC)和活率目标。推定的肿瘤反应性 T 细胞克隆在整个制备过程中得到保留。自体肿瘤刺激后,CD8⁺ T 细胞 4-1BB 和 CD4⁺ T 细胞 OX40 上调,IFN-γ 和 TNF-α 产生增加,体现出功能反应性。体外自体肿瘤类器官杀伤实验进一步证实抗肿瘤活性。结果表明,可从 EC 肿瘤进行体外 TIL 扩增,为启动 II 期 IOV-END-201 临床试验(NCT06481592)评估 lifileucel 治疗晚期 EC 患者提供依据。

展开英文摘要原文

Lifileucel, a tumor-infiltrating lymphocyte (TIL) cell therapy approved for advanced melanoma, demonstrates promise for treating other solid tumors, including endometrial cancer (EC). The current study evaluates the feasibility of manufacturing TILs from EC tumors using Iovance's proprietary 22-day Gen2 manufacturing process. Key parameters, including TIL yield, viability, immune phenotype, T-cell receptor clonality, and cytotoxic activity, were assessed. Of the 11 EC tumor samples processed at research scale, 10 (91%) successfully generated >1 10 9 viable TIL cells, with a median yield of 1.1 10 10 cells and a median viability of 82.8%. Of the four EC tumor samples processed at full scale, all achieved the pre-specified TVC and viability targets. Putative tumor-reactive T-cell clones were maintained throughout the manufacturing process. Functional reactivity was evidenced by the upregulation of 4-1BB in CD8+ T cells, OX40 in CD4+ T cells, and increased production of IFN- and TNF- upon autologous tumor stimulation. Furthermore, antitumor activity was confirmed using an in vitro autologous tumor organoid killing assay. These findings demonstrate the feasibility of ex vivo TIL expansion from EC tumors. This study provides a rationale for the initiation of the phase II clinical trial IOV-END-201 (NCT06481592) to evaluate lifileucel in patients with advanced EC.

论文信息

作者
Zhang Y、Moore KN、Jazaeri AA、Fang J、Patel I、Yuhas A、Innamarato P、Gilbert N
单位
Iovance Biotherapeutics, Inc., San Carlos, CA 94070, USA.United States
期刊
International journal of molecular sciences2025 Jul 24
原文标识
PubMed 40806287 · DOI 10.3390/ijms26157151