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NEO-STIM 推进了个性化新抗原特异性过继性 T 细胞疗法

英文原题:NEO-STIM advances personalized neoantigen-specific adoptive T cell therapy.

查看英文原题

NEO-STIM advances personalized neoantigen-specific adoptive T cell therapy.

PubMed 2026/02/05(内容时间) Nat Commun Q1 · IF 18.1(JCR 2025)

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中文摘要

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。

展开英文摘要原文

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.

论文信息

作者
Lenkala D、Kohler J、McCarthy B、Nelson M、Bakker NAM、de Boer R、Jackson EK、Sheen JHF
第一作者单位
BioNTech US, Cambridge, MA, USA.United States
通讯作者单位
BioNTech US, Cambridge, MA, USA. Marit.vanBuuren@biontech.us.United States
文献类型
I 期临床试验
期刊
Nature communications2026 Feb 5
原文标识
PubMed 41644530 · DOI 10.1038/s41467-026-68680-1