Department of Antibody Discovery and Protein Engineering, MedImmune Ltd, Granta Park, Cambridge, CB21 6GH, UK.
Department of Respiratory, Inflammation and Autoimmunity, MedImmune Ltd, Granta Park, Cambridge, CB21 6GH, UK.
Pharmacol Ther. 2017 Jan;169:113-123. doi: 10.1016/j.pharmthera.2016.04.013. Epub 2016 May 3.
The development of recombinant antibody therapeutics continues to be a significant area of growth in the pharmaceutical industry with almost 50 approved monoclonal antibodies on the market in the US and Europe. Therapeutic drug targets such as soluble cytokines, growth factors and single transmembrane spanning receptors have been successfully targeted by recombinant monoclonal antibodies and the development of new product candidates continues. Despite this growth, however, certain classes of important disease targets have remained intractable to therapeutic antibodies due to the complexity of the target molecules. These complex target molecules include G protein-coupled receptors and ion channels which represent a large target class for therapeutic intervention with monoclonal antibodies. Although these targets have typically been addressed by small molecule approaches, the exquisite specificity of antibodies provides a significant opportunity to provide selective modulation of these important regulators of cell function. Given this opportunity, a significant effort has been applied to address the challenges of targeting these complex molecules and a number of targets are linked to the pathophysiology of respiratory diseases. In this review, we provide a summary of the importance of GPCRs and ion channels involved in respiratory disease and discuss advantages offered by antibodies as therapeutics at these targets. We highlight some recent GPCRs and ion channels linked to respiratory disease mechanisms and describe in detail recent progress made in the strategies for discovery of functional antibodies against challenging membrane protein targets such as GPCRs and ion channels.
重组抗体治疗药物的开发一直是制药行业的一个重要增长领域,在美国和欧洲市场上已有近 50 种批准的单克隆抗体。治疗性药物靶点,如可溶性细胞因子、生长因子和单跨膜受体,已经被重组单克隆抗体成功靶向,并且新的候选药物仍在不断开发。然而,尽管有了这种增长,由于靶分子的复杂性,某些重要疾病靶类仍然无法用治疗性抗体来治疗。这些复杂的靶分子包括 G 蛋白偶联受体和离子通道,它们是治疗性单克隆抗体干预的一个重要靶类。尽管这些靶点通常是通过小分子方法来解决的,但抗体的高度特异性为这些重要细胞功能调节剂的选择性调节提供了一个重要的机会。考虑到这个机会,人们已经付出了巨大的努力来解决靶向这些复杂分子的挑战,并且许多靶点与呼吸疾病的病理生理学有关。在这篇综述中,我们总结了 GPCR 和离子通道在呼吸疾病中的重要性,并讨论了抗体作为这些靶点治疗药物的优势。我们强调了一些与呼吸疾病机制有关的最近的 GPCR 和离子通道,并详细描述了针对 GPCR 和离子通道等具有挑战性的膜蛋白靶点发现功能性抗体的最新策略进展。