单细胞追踪揭示黑色素瘤 TIL 治疗过程中肿瘤反应性 T 细胞的可塑性
Single-cell tracking reveals tumor-reactive T cell plasticity during melanoma TIL therapy.
TIL(肿瘤浸润淋巴细胞)过继细胞治疗可在转移性黑色素瘤中诱导持久缓解,然而在体外扩增过程中及回输后,调控肿瘤反应性T细胞命运的克隆和转录动态仍知之甚少。
英文原题:Feasibility of Manufacturing and Antitumor Activity of TIL for Advanced Endometrial Cancers.
Feasibility of Manufacturing and Antitumor Activity of TIL for Advanced Endometrial Cancers.
这些发现证明了从 EC 肿瘤中体外扩增 TIL 的可行性。
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。
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.
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