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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
和
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