Laboratory of Protein Engineering, Beijing Institute of Biotechnology, Beijing, China.
J Med Virol. 2022 Aug;94(8):3791-3800. doi: 10.1002/jmv.27801. Epub 2022 May 7.
The emerging coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is the causative agent of coronavirus disease 2019 (COVID-19), which has become a severe threat to global public health and local economies. In this study, several single-chain antibody fragments that bind to the receptor-binding domain (RBD) of the SARS-CoV-2 spike (S) protein were identified and used to construct human-mouse chimeric antibodies and humanized antibodies. These antibodies exhibited strong binding to RBD and neutralization activity towards a SARS-CoV-2 pseudovirus. Moreover, these antibodies recognize different RBD epitopes and exhibit synergistic neutralizing activity. These provide candidate to combination use or bispecific antibody to potential clinical therapy for COVID-19.
新兴冠状病毒,严重急性呼吸系统综合症冠状病毒 2(SARS-CoV-2),是造成 2019 年冠状病毒病(COVID-19)的病原体,这已成为严重威胁全球公共健康和地方经济的因素。在这项研究中,鉴定了几种与 SARS-CoV-2 刺突(S)蛋白受体结合域(RBD)结合的单链抗体片段,并用于构建人-鼠嵌合抗体和人源化抗体。这些抗体表现出对 RBD 的强结合和对 SARS-CoV-2 假病毒的中和活性。此外,这些抗体识别不同的 RBD 表位,并表现出协同的中和活性。这些为 COVID-19 的联合使用或双特异性抗体的潜在临床治疗提供了候选。