Industrial Enzymes National Engineering Laboratory, Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin, China.
Institute of Structural Biology, Helmholtz Center Munich, German Research Center for Environmental Health, Neuherberg, Germany.
Curr Pharm Des. 2018;24(41):4932-4946. doi: 10.2174/1381612825666190206105232.
Peptides and proteins are two classes of molecules with attractive possibilities for therapeutic applications. However, the bottleneck for the therapeutic application of many peptides and proteins is their short halflives in vivo, typically just a few minutes to hours. Half-life extension strategies have been extensively studied and many of them have been proven to be effective in the generation of long-acting therapeutics with improved pharmacokinetic and pharmacodynamic properties. In this review, we summarize the recent advances in half-life extension strategies, illustrate their potential applications and give some examples, highlighting the strategies that have been used in approved drugs and for drugs in clinical trials. Meanwhile, several novel strategies that are still in the process of discovery or at a preclinical stage are also introduced. In these strategies, the two most frequently used half-life extension methods are the reduction in the rate of renal clearance or the exploitation of the recycling mechanism of FcRn by binding to the albumin or IgG-Fc. Here, we discuss half-life extension strategies of recombinant therapeutic protein via genetic fusion, rather than chemical conjugation such as PEGylation. With the rapid development of genetic engineering and protein engineering, novel strategies for half-life extension have been emerged consistently. Some of these will be evaluated in clinical trials and may become viable alternatives to current strategies for making next-generation biodrugs.
肽和蛋白质是两类具有治疗应用吸引力的分子。然而,许多肽和蛋白质的治疗应用的瓶颈是它们在体内的半衰期短,通常只有几分钟到几个小时。半衰期延长策略已被广泛研究,其中许多已被证明在生成具有改善的药代动力学和药效学特性的长效治疗药物方面是有效的。在这篇综述中,我们总结了半衰期延长策略的最新进展,说明了它们的潜在应用,并给出了一些例子,突出了已在批准药物和临床试验药物中使用的策略。同时,还介绍了一些仍处于发现过程或临床前阶段的新型策略。在这些策略中,最常使用的两种半衰期延长方法是降低肾脏清除率或通过与白蛋白或 IgG-Fc 结合利用 FcRn 的再循环机制。在这里,我们讨论通过基因融合延长重组治疗蛋白的半衰期的策略,而不是通过化学偶联(如 PEGylation)。随着基因工程和蛋白质工程的快速发展,不断出现新的半衰期延长策略。其中一些将在临床试验中进行评估,并可能成为当前用于制造下一代生物药物的策略的可行替代品。