Hong Yeji, Nam Su-Min, Moon Aree
College of Pharmacy, Duksung Innovative Drug Center, Duksung Women's University, Seoul, 01369, Korea.
Arch Pharm Res. 2023 Mar;46(3):131-148. doi: 10.1007/s12272-023-01433-6. Epub 2023 Mar 6.
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.
使用抗体药物偶联物(ADC)和双特异性抗体(bsAb)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。癌症免疫疗法在检查点阻断和嵌合抗原受体T细胞疗法方面已显示出临床成功;然而,免疫系统过度活跃仍然是一个主要问题。鉴于肿瘤环境的复杂性,采用针对两种或更多分子的策略将具有优势。我们强调了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正在针对多种适应症进行临床开发,具有有前景的治疗活性迹象。ADC包括识别肿瘤抗原的抗体、稳定连接药物的连接子以及强大的细胞毒性药物,也称为有效载荷。ADC通过携带强大的有效载荷靶向癌症而具有直接治疗作用。另一种使用抗体的药物是bsAb,它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。2022年,三种bsAb和一种ADC已获美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准使用。其中,两种bsAb和一种ADC用于癌症治疗。我们在本综述中介绍,ADC和bsAb的组合——双特异性抗体药物偶联物(bsADC)尚未获批,有几种候选药物正处于临床开发的早期阶段。bsADC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偶联策略在ADC和bsAb高效开发中的应用。本综述总结了已获批用于抗癌或目前正在开发的ADC类、bsAb类和bsADC类药物。这些策略可将药物选择性地递送至恶性肿瘤细胞,可用作各类癌症的治疗方法。