Protein Chemistry Department, Genentech, United States.
Methods. 2019 Feb 1;154:102-117. doi: 10.1016/j.ymeth.2018.10.026. Epub 2018 Nov 3.
Bispecific molecules redirecting the cytotoxicity of T-cells are a growing class of therapeutics with numerous molecules being tested in clinical trials. However, it has been a long way since the proof of concept studies in the mid 1980's. In the process we have learnt about the impact of different variables related to the bispecific molecule and the target antigen on the potency of this type of drugs. This work reviews the insights gained and how that knowledge has been used to design more potent bispecific T-cell engagers. The more recent advancement of antibodies with this modality into safety studies in non-human primates and as well as in clinical studies has revealed potential toxicity liabilities for the mode of action. Modifications in existing antibody formats and new experimental molecules designed to mitigate these problems are discussed.
双特异性分子将 T 细胞的细胞毒性重新导向是一类不断发展的治疗药物,许多分子正在临床试验中进行测试。然而,自 20 世纪 80 年代中期的概念验证研究以来,这已经是一条漫长的道路。在此过程中,我们了解到与双特异性分子和靶抗原相关的不同变量对这类药物效力的影响。这项工作回顾了所获得的见解,以及如何利用这些知识来设计更有效的双特异性 T 细胞衔接器。最近,这种模式的抗体在非人类灵长类动物和临床研究中的安全性研究中的进展揭示了作用模式的潜在毒性缺陷。讨论了对现有抗体形式的修改和旨在减轻这些问题的新实验分子。