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A broadly neutralizing monoclonal antibody overcomes the mutational landscape of emerging SARS-CoV-2 variants of concern.

Authors :
Hilal Ahmad Parray
Naveen Narayanan
Sonal Garg
Zaigham Abbas Rizvi
Tripti Shrivastava
Sachin Kushwaha
Janmejay Singh
Praveenkumar Murugavelu
Anbalagan Anantharaj
Farha Mehdi
Nisha Raj
Shivam Singh
Jyotsna Dandotiya
Asha Lukose
Deepti Jamwal
Sandeep Kumar
Adarsh K Chiranjivi
Samridhi Dhyani
Nitesh Mishra
Sanjeev Kumar
Kamini Jakhar
Sudipta Sonar
Anil Kumar Panchal
Manas Ranjan Tripathy
Shirlie Roy Chowdhury
Shubbir Ahmed
Sweety Samal
Shailendra Mani
Sankar Bhattacharyya
Supratik Das
Subrata Sinha
Kalpana Luthra
Gaurav Batra
Devinder Sehgal
Guruprasad R Medigeshi
Chandresh Sharma
Amit Awasthi
Pramod Kumar Garg
Deepak T Nair
Rajesh Kumar
Source :
PLoS Pathogens, Vol 18, Iss 12, p e1010994 (2022)
Publication Year :
2022
Publisher :
Public Library of Science (PLoS), 2022.

Abstract

The emergence of new variants of SARS-CoV-2 necessitates unremitting efforts to discover novel therapeutic monoclonal antibodies (mAbs). Here, we report an extremely potent mAb named P4A2 that can neutralize all the circulating variants of concern (VOCs) with high efficiency, including the highly transmissible Omicron. The crystal structure of the P4A2 Fab:RBD complex revealed that the residues of the RBD that interact with P4A2 are a part of the ACE2-receptor-binding motif and are not mutated in any of the VOCs. The pan coronavirus pseudotyped neutralization assay confirmed that the P4A2 mAb is specific for SARS-CoV-2 and its VOCs. Passive administration of P4A2 to K18-hACE2 transgenic mice conferred protection, both prophylactically and therapeutically, against challenge with VOCs. Overall, our data shows that, the P4A2 mAb has immense therapeutic potential to neutralize the current circulating VOCs. Due to the overlap between the P4A2 epitope and ACE2 binding site on spike-RBD, P4A2 may also be highly effective against a number of future variants.

Details

Language :
English
ISSN :
15537366 and 15537374
Volume :
18
Issue :
12
Database :
Directory of Open Access Journals
Journal :
PLoS Pathogens
Publication Type :
Academic Journal
Accession number :
edsdoj.3ba087963a9548d5823331f44d97566f
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.ppat.1010994