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ImmTAC:基于 T 细胞受体的可溶性双特异性分子的新型平台

英文原题:ImmTAC: A Novel Platform of T-Cell Receptor-Based Soluble Bispecifics.

查看英文原题

ImmTAC: A Novel Platform of T-Cell Receptor-Based Soluble Bispecifics.

PubMed 2026/01/01(内容时间) Methods Mol Biol

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中文摘要

抗癌免疫动员单克隆 T 细胞受体(ImmTAC)分子是一类创新免疫疗法,旨在调动机体免疫系统对抗癌症。其靶向端为可溶性、亲和力增强的 T 细胞受体(TCR),并以共价方式连接一个 CD3 特异性抗体片段作为效应端,从而重定向 T 细胞并杀伤癌细胞。TCR 可识别细胞表面人类白细胞抗原(HLA)呈递的肽段,靶向细胞内抗原谱,从而拓展肿瘤特异性靶点的选择。ImmTAC 平台已获临床验证:tebentafusp 于 2022 年获批用于转移性葡萄膜黑色素瘤,是首个获准商业应用的 TCR 治疗药物,也是首个靶向实体瘤的可溶性双特异性药物。本文介绍可溶性亲和力增强 TCR 及高亲和力 ImmTAC 分子的制备方法。

展开英文摘要原文

Immune mobilizing monoclonal T-cell receptors Against Cancer (ImmTAC ) molecules are innovative immunotherapies designed to harness the body's immune system to fight cancer. They consist of a soluble affinity-enhanced T-cell receptor (TCR) as the targeting arm, covalently linked to an antibody fragment specific to CD3 as the effector arm, enabling T-cell redirection and cancer cell killing.

TCRs can target the intracellular antigenic landscape via recognition of peptides presented by surface localized Human Leukocyte Antigen (HLA) proteins, unlocking a choice of targets that are specific to the tumor. The ImmTAC platform has been validated in the clinic with the approval of tebentafusp in 2022 for the treatment of metastatic uveal melanoma. It is the first TCR therapeutic and first soluble bispecific targeting a solid tumor to be approved for commercial use.

Here, we describe the methods to produce soluble, affinity-enhanced TCRs and high-affinity ImmTAC molecules.

论文信息

作者
Oestringer BP、Vuidepot A
第一作者单位
Immunocore, Abingdon, UK.United Kingdom
通讯作者单位
Immunocore, Abingdon, UK. Annelise.vuidepot@immunocore.com.United Kingdom
期刊
Methods in molecular biology (Clifton, N.J.)2026
原文标识
PubMed 42108342 · DOI 10.1007/978-1-0716-5037-0_4