Merkuleva Yu A, Shcherbakov D N, Ilyichev A A
Vector State Research Center of Virology and Biotechnology, Rospotrebnadzor, World-Class Genomic Research Center for Biological Safety and Technological Independence, Federal Scientific and Technical Program for the Development of Genetic Technologies, 630559 Koltsovo, Novosibirsk oblast Russia.
Russ J Bioorg Chem. 2022;48(2):256-272. doi: 10.1134/S1068162022020169. Epub 2022 May 26.
A viral threat can arise suddenly and quickly turn into a major epidemic or pandemic. In such a case, it is necessary to develop effective means of therapy and prevention in a short time. Vaccine development takes decades, and the use of antiviral compounds is often ineffective and unsafe. A quick response may be the use of convalescent plasma, but a number of difficulties associated with it forced researchers to switch to the development of safer and more effective drugs based on monoclonal antibodies (mAbs). In order to provide protection, such drugs must have a key characteristic-neutralizing properties, i.e., the ability to block viral infection. Currently, there are several approaches to produce mAbs in the researchers' toolkit, however, none of them may serve as a gold standard. Each approach has its own advantages and disadvantages. The choice of the method depends both on the characteristics of the virus and on time constraints and technical challenges. This review provides a comparative analysis of modern methods to produce neutralizing mAbs and describes current trends in the design of antibodies for therapy and prevention of viral diseases.
病毒威胁可能突然出现,并迅速演变成大规模流行病或大流行。在这种情况下,有必要在短时间内开发出有效的治疗和预防手段。疫苗研发需要数十年时间,而使用抗病毒化合物往往既无效又不安全。快速应对措施可能是使用康复期血浆,但与之相关的一些困难迫使研究人员转而研发基于单克隆抗体(mAb)的更安全、更有效的药物。为了提供保护,此类药物必须具备一个关键特性——中和特性,即阻断病毒感染的能力。目前,研究人员的工具包中有几种生产单克隆抗体的方法,但没有一种可作为金标准。每种方法都有其优缺点。方法的选择既取决于病毒的特性,也取决于时间限制和技术挑战。本综述对生产中和性单克隆抗体的现代方法进行了比较分析,并描述了用于治疗和预防病毒性疾病的抗体设计的当前趋势。