Antibody Research Platform, Chongqing International Institute for Immunology, Chongqing, China.
School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing, China.
Front Immunol. 2024 Mar 6;15:1374913. doi: 10.3389/fimmu.2024.1374913. eCollection 2024.
The emergence of SARS-CoV-2 Omicron subvariants has presented a significant challenge to global health, as these variants show resistance to most antibodies developed early in the pandemic. Therapeutic antibodies with potent efficacy to the Omicron variants are urgently demanded.
Utilizing the rapid antibody discovery platform, Berkeley Lights Beacon, we isolated two monoclonal neutralizing antibodies, 2173-A6 and 3462-A4. These antibodies were isolated from individuals who recently recovered from Omicron infections.
Both antibodies, 2173-A6 and 3462-A4, demonstrated high affinity for the RBD and effectively neutralized pseudoviruses from various Omicron lineages, including BA.4/5, XBB.1.16, XBB.1.5, and EG.5.1. This neutralization was achieved through binding to identical or overlapping epitopes.
The use of the Beacon platform enabled the rapid isolation and identification of effective neutralizing antibodies within less than 10 days. This process significantly accelerates the development of novel therapeutic antibodies, potentially reducing the time required to respond to unknown infectious diseases in the future.
SARS-CoV-2 奥密克戎亚变种的出现对全球健康构成了重大挑战,因为这些变种对大流行早期开发的大多数抗体表现出耐药性。迫切需要对奥密克戎变体具有强大疗效的治疗性抗体。
我们利用快速抗体发现平台——伯克利之光 Beacon,从最近从奥密克戎感染中康复的个体中分离出两种单克隆中和抗体 2173-A6 和 3462-A4。
两种抗体 2173-A6 和 3462-A4 均对 RBD 具有高亲和力,并能有效中和来自各种奥密克戎谱系的假病毒,包括 BA.4/5、XBB.1.16、XBB.1.5 和 EG.5.1。这种中和作用是通过与相同或重叠的表位结合实现的。
Beacon 平台的使用使得在不到 10 天的时间内快速分离和鉴定有效的中和抗体成为可能。这一过程显著加快了新型治疗性抗体的开发速度,可能会缩短未来应对未知传染病所需的时间。