Ontology highlight
ABSTRACT: Background
The introduction of new SARS-CoV-2 Omicron strains has made it extremely difficult to create broadly neutralizing antibodies (nAbs) with assured therapeutic potential. Currently approved neutralizing antibodies have displayed substantially decreased or abolished efficacy against emerging Omicron variants including XBB and BQ.1 Due to the potential of reinfection from new emerging VOCs, this emphasizes the urgent need for developing widely active mAbs that offer preventive and therapeutic advantages to high-risk patients. Here, we aimed to investigate the feasibility of redirecting existing mAbs which are in late-stage development in clinical trials against new variants of SARS-CoV-2.Methods
In vitro affinity maturation libraries against BA.2 RBD were constructed
SUBMITTER: Huang Y
PROVIDER: S-EPMC12584199 | biostudies-literature | 2025 Nov
REPOSITORIES: biostudies-literature