<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>39(8)</volume><submitter>Wang S</submitter><pubmed_abstract>The rapidly spreading Omicron variant is highly resistant to vaccines, convalescent sera, and neutralizing antibodies (nAbs), highlighting the urgent need for potent therapeutic nAbs. Here, a panel of human nAbs from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) convalescent patients show diverse neutralization against Omicron, of which XMA01 and XMA04 maintain nanomolar affinities and excellent neutralization (half maximal inhibitory concentration [IC50]: ∼20 ng/mL). nAb XMA09 shows weak but unattenuated neutralization against all variants of concern (VOCs) as well as SARS-CoV. Structural analysis reveals that the above three antibodies could synergistically bind to the receptor-binding domains (RBDs) of both wild-type and Omicron spikes and defines the critical determinant</pubmed_abstract><journal>Cell reports</journal><pagination>110862</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9080080</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Three SARS-CoV-2 antibodies provide broad and synergistic neutralization against variants of concern, including Omicron.</pubmed_title><pmcid>PMC9080080</pmcid><pubmed_authors>Tang Z</pubmed_authors><pubmed_authors>Zheng Z</pubmed_authors><pubmed_authors>Liu L</pubmed_authors><pubmed_authors>Zhang J</pubmed_authors><pubmed_authors>Yuan Q</pubmed_authors><pubmed_authors>Yuan L</pubmed_authors><pubmed_authors>Zheng Q</pubmed_authors><pubmed_authors>Yu H</pubmed_authors><pubmed_authors>Cheng T</pubmed_authors><pubmed_authors>Guan Y</pubmed_authors><pubmed_authors>Zhang T</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Li T</pubmed_authors><pubmed_authors>Chen Z</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Ying D</pubmed_authors><pubmed_authors>Xia N</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Sun H</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Xiong H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Three SARS-CoV-2 antibodies provide broad and synergistic neutralization against variants of concern, including Omicron.</name><description>The rapidly spreading Omicron variant is highly resistant to vaccines, convalescent sera, and neutralizing antibodies (nAbs), highlighting the urgent need for potent therapeutic nAbs. Here, a panel of human nAbs from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) convalescent patients show diverse neutralization against Omicron, of which XMA01 and XMA04 maintain nanomolar affinities and excellent neutralization (half maximal inhibitory concentration [IC50]: ∼20 ng/mL). nAb XMA09 shows weak but unattenuated neutralization against all variants of concern (VOCs) as well as SARS-CoV. Structural analysis reveals that the above three antibodies could synergistically bind to the receptor-binding domains (RBDs) of both wild-type and Omicron spikes and defines the critical determinant</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2026-05-31T05:03:59.828Z</modification><creation>2025-02-19T01:54:56.63Z</creation></dates><accession>S-EPMC9080080</accession><cross_references><pubmed>35594869</pubmed><doi>10.1016/j.celrep.2022.110862</doi></cross_references></HashMap>