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一种 TCR 样嵌合抗原受体通过 mRNA 疫苗接种促进敏感的抗原识别和受控的 T 细胞扩增。

A TCR-like CAR Promotes Sensitive Antigen Recognition and Controlled T-cell Expansion Upon mRNA Vaccination.

机构信息

TRON - Translational Oncology at the University Medical Center of the Johannes Gutenberg University gGmbH (non-profit), Mainz, Germany.

Biopharmaceutical New Technologies (BioNTech) Corporation, BioNTech Cell & Gene Therapies GmbH, Mainz, Germany.

出版信息

Cancer Res Commun. 2022 Aug 18;2(8):827-841. doi: 10.1158/2767-9764.CRC-21-0154. eCollection 2022 Aug.

Abstract

UNLABELLED

Chimeric antigen receptor (CAR) T cells are efficacious in patients with B-cell malignancies, while their activity is limited in patients with solid tumors. We developed a novel heterodimeric TCR-like CAR (TCAR) designed to achieve optimal chain pairing and integration into the T-cell CD3 signaling complex. The TCAR mediated high antigen sensitivity and potent antigen-specific T-cell effector functions in short-term assays. Both persistence and functionality of TCAR T cells were augmented by provision of costimulatory signals, which improved proliferation and . Combination with a nanoparticulate RNA vaccine, developed for expansion of CAR T cells, promoted tightly controlled expansion, survival, and antitumor efficacy of TCAR T cells .

SIGNIFICANCE

A novel TCAR is tightly controlled by RNA vaccine-mediated costimulation and may provide an alternative to second-generation CARs for the treatment of solid tumors.

摘要

未注明

嵌合抗原受体 (CAR) T 细胞在 B 细胞恶性肿瘤患者中有效,而在实体瘤患者中其活性有限。我们开发了一种新型的异二聚体 TCR 样 CAR(TCAR),旨在实现最佳的链配对和整合到 T 细胞 CD3 信号复合物中。TCAR 介导高抗原敏感性和有效的抗原特异性 T 细胞效应功能在短期分析中。通过提供共刺激信号,TCAR T 细胞的持久性和功能得到增强,这提高了增殖和细胞因子产生。与纳米颗粒 RNA 疫苗结合,该疫苗用于 CAR T 细胞的扩增,促进了 TCAR T 细胞的严格控制扩增、存活和抗肿瘤疗效。

意义

一种新型的 T CAR 受 RNA 疫苗介导的共刺激的严格控制,可能为治疗实体瘤提供替代第二代 CAR 的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73d9/10010320/bdc26cbea5db/crc-21-0154_fig1.jpg

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