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一种用于小鼠癌症免疫治疗的树突状细胞疫苗,既可用于疫苗接种,也可用于新抗原反应性 T 细胞的制备

英文原题:A dendritic cell vaccine for both vaccination and neoantigen-reactive T cell preparation for cancer immunotherapy in mice.

PubMed 2024/11/29(内容时间) Nat Commun Q1 · IF 18.1(JCR 2025)

研究概要

我们提出了一种制备NRTs的方法,该方法提高了ACT疗效,并为个性化免疫疗法的设计铺平了道路。

中文摘要

使用新抗原特异性 T 细胞的过继细胞转移(ACT)是一种有效的免疫治疗策略。然而,新抗原特异性 T 细胞难以分离,限制了 ACT 的临床应用。在此,我们提出了一种在负载肿瘤裂解物的树突状细胞(DC)疫苗免疫后制备用于 ACT 的新抗原反应性 T 细胞(NRT)的方法。我们表明,该 DC 疫苗不仅在体内在荷肺癌小鼠中诱导新抗原反应性免疫应答,而且在体外促进 NRT 细胞的制备。将 NRT 作为联合疗法过继转移至 DC 疫苗免疫的 LL/2 荷瘤小鼠中,可使输注的 NRT 浸润,以及新抗原反应性、非 ACT/NRT T 细胞富集到肿瘤微环境中,这些新抗原反应性 T 细胞受体的功能在体外得到验证。总之,我们提出了一种制备 NRT 的方法,可提高 ACT 疗效,并为个性化免疫疗法的设计铺平道路。

展开英文摘要原文

Adoptive cell transfer (ACT) using neoantigen-specific T cells is an effective immunotherapeutic strategy. However, the difficult isolation of neoantigen-specific T cells limits the clinical application of ACT. Here, we propose a method to prepare neoantigen-reactive T cells (NRT) for ACT following immunization with a tumor lysate-loaded dendritic cell (DC) vaccine. We show that the DC vaccine not only induces a neoantigen-reactive immune response in lung cancer-bearing mice in vivo, but also facilitate NRT cell preparation in vitro. Adoptive transfer of the NRTs as combinatorial therapy into DC vaccine-immunized, LL/2 tumor-bearing mice allows infiltration of the infused NRTs, as well as the enrichment of neoantigen reactive, non-ACT/NRT T cells into the tumor microenvironment with the function of these neoantigen-reactive T-cell receptors validated in vitro. In summary, we propose a method for preparing NRTs that increases ACT efficacy and paves the way to the design of personalized immunotherapies.

论文信息

作者
Li Q、Zeng H、Liu T、Wang P、Zhang R、Zhao B、Feng T、Yang Y
第一作者单位
Department of Biotherapy, Cancer Center, National Clinical Research Center for Geriatrics, West China Hospital, Sichuan University, Chengdu, China.China
通讯作者单位
Department of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China. dingzhenyu@scu.edu.cn.China
文献类型
非美国政府资助研究
期刊
Nature communications2024 Nov 29
原文标识
PubMed 39613742 · DOI 10.1038/s41467-024-54650-y