针对癌症的抗体-药物偶联物和双特异性抗体:点击化学的应用

IF 6.9 3区 医学 Q1 CHEMISTRY, MEDICINAL Archives of Pharmacal Research Pub Date : 2023-03-06 DOI:10.1007/s12272-023-01433-6
Yeji Hong, Su-Min Nam, Aree Moon
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引用次数: 12

摘要

使用抗体药物偶联物(adc)和双特异性抗体(bsAbs)的工程方法旨在克服传统化疗和治疗性抗体的局限性,如耐药性和非特异性毒性。癌症免疫疗法已被证明是临床成功的检查点阻断和嵌合抗原受体T细胞治疗;然而,过度活跃的免疫系统仍然是一个主要问题。考虑到肿瘤环境的复杂性,针对两个或更多分子的策略将是有利的。我们强调针对癌症的多靶点平台策略的必要性和重要性。目前,约有400种adc和200多种bsab正在临床开发,用于几种适应症,具有良好的治疗活性迹象。adc包括识别肿瘤抗原的抗体,稳定连接药物的连接物,以及强大的细胞毒性药物,也被称为有效载荷。adc通过靶向具有强有效载荷的癌症具有直接的治疗作用。另一种使用抗体的药物是bsab,通过连接抗原识别位点或桥接细胞毒性免疫细胞与肿瘤细胞来靶向两种抗原,从而实现癌症免疫治疗。三种bsab和一种ADC已于2022年被FDA和EMA批准使用。其中,两种bsab和一种ADC用于癌症。我们在本综述中介绍了bsADC, ADC和bsab的组合,尚未获得批准,几个候选药物处于临床开发的早期阶段。bsADCs技术有助于提高adc的特异性或bsab的内化和杀伤能力。我们还简要讨论了点击化学作为一种共轭策略在adc和bsab的高效开发中的应用。本文综述了已获批或正在开发的adc、bsab和bsADCs。这些策略选择性地将药物输送到恶性肿瘤细胞,并可作为治疗各种类型癌症的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Antibody–drug conjugates and bispecific antibodies targeting cancers: applications of click chemistry

Engineering approaches using antibody drug conjugates (ADCs) and bispecific antibodies (bsAbs) are designed to overcome the limitations of conventional chemotherapies and therapeutic antibodies such as drug resistance and non-specific toxicity. Cancer immunotherapies have been shown to be clinically successful with checkpoint blockade and chimeric antigen receptor T cell therapy; however, overactive immune systems still represent a major problem. Given the complexity of a tumor environment, it would be advantageous to have a strategy targeting two or more molecules. We highlight the necessity and importance of a multi-target platform strategy against cancer. Approximately 400 ADCs and over 200 bsAbs are currently being clinically developed for several indications, with promising signs of therapeutic activity. ADCs include antibodies that recognize tumor antigens, linkers that stably connect drugs, and powerful cytotoxic drugs, also known as payloads. ADCs have direct therapeutic effects by targeting cancers with a strong payload. Another type of drug that uses antibodies are bsAbs, targeting two antigens by linking to antigen recognition sites or bridging cytotoxic immune cells to tumor cells, resulting in cancer immunotherapy. Three bsAbs and one ADC have been approved for use by the FDA and the EMA in 2022. Among these, two of the bsAbs and the one ADC are used for cancers. We introduced that bsADC, a combination of ADC and bsAbs, has yet to be approved and several candidates are in the early stages of clinical development in this review. bsADCs technology helps increase the specificity of ADCs or the internalization and killing ability of bsAbs. We also briefly discuss the application of click chemistry in the efficient development of ADCs and bsAbs as a conjugation strategy. The present review summarizes the ADCs, bsAbs, and bsADCs that have been approved for anti-cancer or currently in development. These strategies selectively deliver drugs to malignant tumor cells and can be used as therapeutic approaches for various types of cancer.

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来源期刊
CiteScore
13.40
自引率
9.00%
发文量
48
审稿时长
3.3 months
期刊介绍: Archives of Pharmacal Research is the official journal of the Pharmaceutical Society of Korea and has been published since 1976. Archives of Pharmacal Research is an interdisciplinary journal devoted to the publication of original scientific research papers and reviews in the fields of drug discovery, drug development, and drug actions with a view to providing fundamental and novel information on drugs and drug candidates.
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