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Cellectis在 AACR-IO 2025上展示“智能 CAR T”策略以提高对实体瘤的疗效

Cellectis Presents ‘Smart CAR T’ Strategy to Enhance Efficacy Against Solid Tumors at AACR-IO 2025

Cellectis 等信源发布 2025-02-24 14:37

可切换为仅中文


New York, NY – February 24, 2025

美国纽约州纽约市——2025年2月24日

- Cellectis (the “Company”) (Euronext Growth: ALCLS - NASDAQ: CLLS), a clinical-stage biotechnology company using its pioneering gene-editing platform to develop life-saving cell and gene therapies, showcases an innovative strategy for T cell engineering that leverages the pro-inflammatory properties of interleukin 2 (IL-2) with the objective to enhance CAR T cell efficacy against solid tumors, at the American Association for Cancer Research – Immuno-oncology (AACR-IO), taking place on February 23-26, 2025 in Los Angeles, CA.

Cellectis(“公司”)(泛欧交易所成长板:ALCLS - 纳斯达克:CLLS),一家处于临床阶段的生物技术公司,利用其开创性的基因编辑平台开发挽救生命的细胞和基因疗法,展示了一种创新的T细胞工程策略,该策略利用白细胞介素2(IL-2)的促炎特性,旨在增强CAR-T细胞对实体瘤的疗效。这一展示将在2025年2月23日至26日于加利福尼亚州洛杉矶举行的美国癌症研究协会-免疫肿瘤学(AACR-IO)会议上进行。

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The data are presented in a poster:

数据以海报形式呈现:

CAR induced expression of synthetically engineered FAP-IL2v immunocytokine boosts persistent anti-tumor activity of TALEN-edited allogeneic CAR T-cells without associated IL-2 toxicity

CAR诱导合成工程FAP-IL2v免疫细胞因子的表达,增强TALEN编辑的同种异体CAR T细胞的持久抗肿瘤活性,且无相关IL-2毒性。

Presenter:

主持人:

Shipra Das, Ph.D., Associate Director Immuno-Oncology, at Cellectis.

Shipra Das,博士,Cellectis公司免疫肿瘤学副总监。

Date/Time:

日期/时间:

February 25,

2月25日,

2025,

2025,

1:45-4:45 p.m. PT

下午1:45-4:45(太平洋时间)

Session

会话

: Poster Session B

:海报会议 B

CAR T-cell therapies have transformed the treatment landscape for specific hematological malignancies and have shown promising preliminary efficacy in solid tumors.

CAR T细胞疗法已经改变了特定血液系统恶性肿瘤的治疗格局,并在实体瘤中显示出有希望的初步疗效。

Recent studies suggest a link between the

最近的研究表明两者之间存在联系

in vivo

体内

expansion and persistence of CAR-T cells and enhanced therapeutic outcomes in patients. The co-administration of interleukin-2 (IL-2) has been demonstrated to improve CAR T-cell engraftment, expansion, and functionality in preclinical models but poses toxicity risks at high doses.

CAR-T细胞的扩增和持久性以及患者治疗效果的增强。白细胞介素-2(IL-2)的共同给药已被证明在临床前模型中可以改善CAR-T细胞的植入、扩增和功能,但在高剂量下存在毒性风险。

Using Cellectis’ TALEN

使用Cellectis的TALEN技术

®

®

gene editing technology, we developed ‘Smart CAR T cells’ with the ability to express a CAR-inducible IL-2 variant (IL-2v) immunocytokine, potentiated by tumor-specific cues for localized activity within the solid tumor microenvironment (TME).

通过基因编辑技术,我们开发了“智能CAR-T细胞”,这种细胞能够在肿瘤特异性信号的刺激下表达一种CAR诱导的IL-2变体(IL-2v)免疫细胞因子,并在实体瘤微环境(TME)中发挥局部活性。

CAR-inducible expression of this recombinant FAP

CAR诱导的这种重组FAP的表达

scFv

单链抗体片段

-IL2v boosts anti-tumor activity of engineered CAR T-cells both

-IL2v 增强了工程化 CAR T 细胞的抗肿瘤活性

in vitro

体外

and

in vivo

体内

. Notably, the enhancement of CAR T-cell activity mediated by IL-2v relies on its anchoring to the FAP protein, which is uniquely present in the TME, thus minimizing the systemic toxicity typically associated with circulating free IL-2 cytokines.

特别是,IL-2v介导的CAR T细胞活性增强依赖于其锚定在TME中独特存在的FAP蛋白上,从而最大限度地减少了通常与循环游离IL-2细胞因子相关的全身毒性。

This proposed cellular engineering strategy would represent an effective and safe method to substantially improve CAR T cell expansion and anti-tumor activity, while confining IL-2 activity to the tumor microenvironment.

该拟议的细胞工程策略将代表一种有效且安全的方法,可在大幅改善CAR T细胞扩增和抗肿瘤活性的同时,将IL-2活性限制在肿瘤微环境中。

The poster is published on

海报发布于

Cellectis’ website

Cellectis的网站

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Download the PDF file

下载PDF文件