葡萄糖剥夺的肿瘤微环境激活 AMP 活化蛋白激酶驱动过继转移的 T 辅助 9 细胞衰老
Glucose-deprived tumor microenvironment activates AMP-activated protein kinase to drive adoptively transferred T helper 9 cell senescence.
辅助性T细胞9(Th9)细胞在针对实体瘤的过继细胞治疗(ACT)中显示出前景。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:NEO-STIM advances personalized neoantigen-specific adoptive T cell therapy.
NEO-STIM advances personalized neoantigen-specific adoptive T cell therapy.
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基于新抗原的过继性T细胞疗法(ACT)因其卓越的肿瘤特异性,在癌症免疫治疗中代表了一条有前景的途径。首个用于实体瘤的细胞免疫疗法,由TIL(肿瘤浸润淋巴细胞)组成,最近获得了FDA批准。在此基础上,我们设计了一种独特的ACT方法,即从自体外周血中系统性地产生针对个体化新抗原的T细胞应答。在此,我们报道了NEO-STIM的建立,这是一种体外诱导过程,用于激活和扩增预先存在的记忆性以及新产生的CD8+和CD4+ T细胞应答,从而突显了产生强效新抗原特异性T细胞应答的关键参数。药物产品包含突变反应性、多功能且具有细胞毒性的CD8+和CD4+ T细胞,能够识别自体肿瘤物质。输注后,在患者的肿瘤和血液中检测到T细胞应答,并显示出活化/耗竭及细胞毒性表型。一项首次人体临床试验(NCT04625205)最近进一步验证了概念验证,支持该ACT方法的持续开发。
Neoantigen-based adoptive T cell therapies (ACTs) represent a promising avenue in cancer immunotherapy due to their exquisite tumor specificity. The first cell-based immunotherapy for a solid tumor, comprising tumor-infiltrating lymphocytes, recently received FDA approval. Building on this, we designed a distinct ACT approach, where T cell responses against personalized neoantigens are systematically generated from autologous peripheral blood.
Here we report the establishment of NEO-STIM, an ex vivo induction process to prime and expand pre-existing memory and de novo CD8 + and CD4 + T cell responses, thereby highlighting critical parameters for generating potent neoantigen-specific T cell responses. The drug products comprise mutant-reactive, polyfunctional, and cytotoxic CD8 + and CD4 + T cells, able to recognize autologous tumor material.
Following infusion, T cell responses are detected in tumor and blood of a patient, and display activated/exhausted and cytotoxic phenotypes. A first-in-human clinical trial (NCT04625205) recently further validated proof-of-concept, supporting continued development of this ACT approach.
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