SARS-CoV-2 variant evasion of monoclonal antibodies based on in vitro studies

Alessandro M. Carabelli, MacGregor Cox, Thomas P Peacock, Will Harvey, Joseph Hughes, Derek Wright, Brian J. Willett, Emma Thompson, Ravinda Gupta, Sharon J Peacock, David L Robertson, The COVID-19 Genomics UK (COG-UK) Consortium [NRMICRO-22-182-TV4] The COVID-19 Genomics UK (COG-UK) Consortium [NRMICRO-22-182-TV4]

Research output: Contribution to journalReview articlepeer-review


Monoclonal antibodies (mAbs) offer a treatment option for individuals with severe COVID-19 and are especially important in high-risk individuals where vaccination is not an option. Given the importance of understanding the evolution of resistance to mAbs by SARS-CoV-2, we reviewed the available in vitro neutralization data for mAbs against live variants and viral constructs containing spike mutations of interest. Unfortunately, evasion of mAb-induced protection is being reported with new SARS-CoV-2 variants. The magnitude of neutralization reduction varied greatly among mAb-variant pairs. For example, sotrovimab retained its neutralization capacity against Omicron BA.1 but showed reduced efficacy against BA.2, BA.4 and BA.5, and BA.2.12.1. At present, only bebtelovimab has been reported to retain its efficacy against all SARS-CoV-2 variants considered here. Resistance to mAb neutralization was dominated by the action of epitope single amino acid substitutions in the spike protein. Although not all observed epitope mutations result in increased mAb evasion, amino acid substitutions at non-epitope positions and combinations of mutations also contribute to evasion of neutralization. This Review highlights the implications for the rational design of viral genomic surveillance and factors to consider for the development of novel mAb therapies.

Original languageEnglish
Article number3013
Pages (from-to)1-13
Number of pages13
JournalNature Reviews Microbiology
Early online date28 Oct 2022
Publication statusE-pub ahead of print - 28 Oct 2022


Dive into the research topics of 'SARS-CoV-2 variant evasion of monoclonal antibodies based on in vitro studies'. Together they form a unique fingerprint.

Cite this