University for International Integration of the Afro-Brazilian Lusophony, Institute of Health Sciences, Ceara, Brazil.
Federal University of Ceara, College of Medicine, Department of Physiology and Pharmacology, Fortaleza, Ceara, Brazil.
Curr Med Chem. 2021;28(13):2485-2520. doi: 10.2174/0929867327666200525161359.
Targeted therapy has been recently highlighted due to the reduction of side effects and improvement in overall efficacy and survival from different types of cancers. Considering the approval of many monoclonal antibodies in the last twenty years, cancer treatment can be accomplished by the combination of monoclonal antibodies and small molecule chemotherapeutics. Thus, strategies to combine both drugs in a single administration system are relevant in the clinic. In this context, two strategies are possible and will be further discussed in this review: antibody-drug conjugates (ADCs) and antibody-functionalized nanoparticles. First, it is important to better understand the possible molecular targets for cancer therapy, addressing different antigens that can selectively bind to antibodies. After selecting the best target, ADCs can be prepared by attaching a cytotoxic drug to an antibody able to target a cancer cell antigen. Briefly, an ADC will be formed by a monoclonal antibody (MAb), a cytotoxic molecule (cytotoxin) and a chemical linker. Usually, surface-exposed lysine or the thiol group of cysteine residues are used as anchor sites for linker-drug molecules. Another strategy that should be considered is antibody-functionalized nanoparticles. Basically, liposomes, polymeric and inorganic nanoparticles can be attached to specific antibodies for targeted therapy. Different conjugation strategies can be used, but nanoparticles coupling between maleimide and thiolated antibodies or activation with the addition of ethyl-3-(3-dimethyl aminopropyl) carbodiimide (EDC)/ N-hydroxysuccinimide (NHS) (1:5) and further addition of the antibody are some of the most used strategies. Herein, molecular targets and conjugation strategies will be presented and discussed to better understand the in vitro and in vivo applications presented. Also, the clinical development of ADCs and antibody-conjugated nanoparticles are addressed in the clinical development section. Finally, due to the innovation related to the targeted therapy, it is convenient to analyze the impact on patenting and technology. Information related to the temporal evolution of the number of patents, distribution of patent holders and also the number of patents related to cancer types are presented and discussed. Thus, our aim is to provide an overview of the recent developments in immunoconjugates for cancer targeting and highlight the most important aspects for clinical relevance and innovation.
近年来,由于减少了副作用,提高了不同类型癌症的整体疗效和生存率,靶向治疗受到了关注。考虑到过去 20 年批准了许多单克隆抗体,癌症治疗可以通过单克隆抗体和小分子化疗药物的联合来完成。因此,将这两种药物结合在单一给药系统中的策略在临床上是相关的。在这种情况下,有两种策略是可能的,并且在本文中将进一步讨论:抗体药物偶联物(ADC)和抗体功能化纳米颗粒。首先,更好地了解癌症治疗的可能分子靶点很重要,针对可以选择性结合抗体的不同抗原。在选择最佳靶标后,可以通过将细胞毒性药物连接到能够靶向癌细胞抗原的抗体上来制备 ADC。简而言之,ADC 将由单克隆抗体(MAb)、细胞毒性分子(细胞毒素)和化学连接子组成。通常,表面暴露的赖氨酸或半胱氨酸残基的巯基用作连接子-药物分子的锚定点。另一种需要考虑的策略是抗体功能化纳米颗粒。基本上,脂质体、聚合物和无机纳米颗粒可以连接到用于靶向治疗的特定抗体上。可以使用不同的偶联策略,但最常用的策略是马来酰亚胺和巯基化抗体之间的纳米颗粒偶联或通过添加乙基-3-(3-二甲基氨基丙基)碳二亚胺(EDC)/N-羟基琥珀酰亚胺(NHS)(1:5)进行激活,然后添加抗体。本文将介绍和讨论分子靶点和偶联策略,以更好地了解体外和体内应用。此外,还在临床开发部分中讨论了 ADC 和抗体偶联纳米颗粒的临床开发。最后,由于靶向治疗的创新性,分析其对专利和技术的影响是很方便的。介绍并讨论了与专利数量的时间演变、专利持有者的分布以及与癌症类型相关的专利数量相关的信息。因此,我们的目的是提供癌症靶向免疫缀合物的最新发展概述,并强调与临床相关性和创新性相关的最重要方面。