Richards Daniel A
Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK.
Drug Discov Today Technol. 2018 Dec;30:35-46. doi: 10.1016/j.ddtec.2018.10.005. Epub 2018 Nov 8.
The field of targeted therapeutics has benefitted immeasurably from the development of high-affinity antibodies. These important ligands have facilitated the development of effective therapies, particularly when conjugated to potent cytotoxic payloads i.e. in antibody-drug conjugates (ADCs). The success of ADCs is evidenced by rapid adoption within the pharmaceuticals community; many major companies have dedicated ADC research programmes. However, despite the advantages, the field of ADCs has failed to live up to its full potential. Studies have emerged suggesting that traditional IgG scaffolds may not be the optimal format for targeted payload delivery. In response, the protein engineering community has begun to explore alternative high-binding protein scaffolds as antibody mimics. In this short review I will summarise the generation, modification, and application of emerging antibody fragments and synthetic antibody mimics, with a focus on their use as drug carriers. The review aims to highlight the advantages of antibody mimics, and how they could be employed to overcome the issues and limitations of traditional ADCs.
靶向治疗领域从高亲和力抗体的发展中受益匪浅。这些重要的配体推动了有效疗法的开发,特别是当与强效细胞毒性载荷偶联时,即抗体药物偶联物(ADC)。ADC在制药界迅速得到应用,证明了其成功;许多大公司都有专门的ADC研究项目。然而,尽管有这些优势,ADC领域尚未充分发挥其潜力。有研究表明,传统的IgG支架可能不是靶向载荷递送的最佳形式。作为回应,蛋白质工程界已开始探索替代的高结合蛋白支架作为抗体模拟物。在这篇简短的综述中,我将总结新兴抗体片段和合成抗体模拟物的产生、修饰及应用,重点关注它们作为药物载体的用途。这篇综述旨在突出抗体模拟物的优势,以及它们如何被用于克服传统ADC的问题和局限性。