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A multispecific antibody confers pan-reactive SARS-CoV-2 neutralization and prevents immune escape.


ABSTRACT: Continued evolution of the SARS-CoV-2 spike poses a challenge to immune interventions. To develop antibodies that protect against evolving SARS-CoV-2 viruses, we combined antibodies that recognize different RBD sites to generate a trivalent antibody that potently neutralized all major variants, including the most recent Omicron lineages. Negative stain electron microscopy suggests that this multispecific achieves synergistic neutralization by engaging different epitopes in specific orientations that facilitate inter-spike binding. These interactions resulted in not only improved potency but also importantly prevented virus escape, a feature not seen with parental antibody cocktails or the most potent clinical antibody. Such multispecific antibodies simplify treatment, maximize coverage, decrease the likelihood of SARS-CoV-2 escape, and provide the basis for building universal SARS-CoV-2 antibody therapies that are more likely to maintain broad reactivity for future variants.

SUBMITTER: Misasi J 

PROVIDER: S-EPMC9387125 | biostudies-literature | 2022 Aug

REPOSITORIES: biostudies-literature

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A multispecific antibody prevents immune escape and confers pan-SARS-CoV-2 neutralization.

Misasi John J   Wei Ronnie R RR   Wang Lingshu L   Pegu Amarendra A   Wei Chih-Jen CJ   Oloniniyi Olamide K OK   Zhou Tongqing T   Moliva Juan I JI   Zhao Bingchun B   Choe Misook M   Yang Eun Sung ES   Zhang Yi Y   Boruszczak Marika M   Chen Man M   Leung Kwan K   Li Juan J   Yang Zhi-Yong ZY   Andersen Hanne H   Carlton Kevin K   Godbole Sucheta S   Harris Darcy R DR   Henry Amy R AR   Ivleva Vera B VB   Lei Paula P   Liu Cuiping C   Longobardi Lindsay L   Merriam Jonah S JS   Nase Danielle D   Olia Adam S AS   Pessaint Laurent L   Porto Maciel M   Shi Wei W   Wolff Jeremy J JJ   Douek Daniel C DC   Suthar Mehul S MS   Gall Jason J   Koup Richard A RA   Kwong Peter D PD   Mascola John R JR   Nabel Gary J GJ   Sullivan Nancy J NJ  

bioRxiv : the preprint server for biology 20221121


Despite effective countermeasures, SARS-CoV-2 persists worldwide due to its ability to diversify and evade human immunity<sup>1</sup>. This evasion stems from amino-acid substitutions, particularly in the receptor-binding domain of the spike, that confer resistance to vaccines and antibodies <sup>2-16</sup>. To constrain viral escape through resistance mutations, we combined antibody variable regions that recognize different receptor binding domain (RBD) sites<sup>17,18</sup> into multispecific  ...[more]

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