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基于双特异性抗体的免疫细胞衔接器及其在肿瘤免疫治疗中的新兴治疗靶点

英文原题:Bispecific Antibody-Based Immune-Cell Engagers and Their Emerging Therapeutic Targets in Cancer Immunotherapy.

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Bispecific Antibody-Based Immune-Cell Engagers and Their Emerging Therapeutic Targets in Cancer Immunotherapy.

PubMed 2022/05/19(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

癌症是全球第二大死因,仅次于心血管疾病。利用免疫细胞的功能是增强肿瘤免疫治疗抗肿瘤效应的一种有前景的策略。重组 DNA 技术和抗体工程的近期进展开启了基于双特异性抗体(bsAb)的免疫细胞衔接器(ICE)新时代,其中包括 T 细胞和NK 细胞衔接器。自美国食品药品监督管理局(FDA)首次批准 blinatumomab 以来,多种基于 bsAb 的 ICE 已被开发用于有效治疗癌症患者;与此同时,人们也在多种癌症中发现了若干潜在治疗靶点。因此,本文综述 bsAb 类 ICE 的作用机制、设计与结构、临床开发进展及其获 FDA 批准用于人类恶性肿瘤治疗的情况,并总结目前已知及新兴的治疗靶点。本文还为下一代 ICE 的开发提供实际考量方面的见解。

展开英文摘要原文

Cancer is the second leading cause of death worldwide after cardiovascular diseases. Harnessing the power of immune cells is a promising strategy to improve the antitumor effect of cancer immunotherapy. Recent progress in recombinant DNA technology and antibody engineering has ushered in a new era of bispecific antibody (bsAb)-based immune-cell engagers (ICEs), including T- and natural-killer-cell engagers.

Since the first approval of blinatumomab by the United States Food and Drug Administration (US FDA), various bsAb-based ICEs have been developed for the effective treatment of patients with cancer. Simultaneously, several potential therapeutic targets of bsAb-based ICEs have been identified in various cancers.

Therefore, this review focused on not only highlighting the action mechanism, design and structure, and status of bsAb-based ICEs in clinical development and their approval by the US FDA for human malignancy treatment, but also on summarizing the currently known and emerging therapeutic targets in cancer. This review provides insights into practical considerations for developing next-generation ICEs.

论文信息

作者
Shin HG、Yang HR、Yoon A、Lee S
单位
Department of Biopharmaceutical Chemistry, College of Science and Technology, Kookmin University, Seoul 02707, Korea.South Korea
文献类型
综述
期刊
International journal of molecular sciences2022 May 19
原文标识
PubMed 35628495 · DOI 10.3390/ijms23105686