<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Park YJ</submitter><funding>Howard Hughes Medical Institute</funding><funding>NIAID NIH HHS</funding><funding>NIH HHS</funding><pagination>619-627</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12945441</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>378(6620)</volume><pubmed_abstract>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron sublineages carry distinct spike mutations resulting in escape from antibodies induced by previous infection or vaccination. We show that hybrid immunity or vaccine boosters elicit plasma-neutralizing antibodies against Omicron BA.1, BA.2, BA.2.12.1, and BA.4/5, and that breakthrough infections, but not vaccination alone, induce neutralizing antibodies in the nasal mucosa. Consistent with immunological imprinting, most antibodies derived from memory B cells or plasma cells of Omicron breakthrough cases cross-react with the Wuhan-Hu-1, BA.1, BA.2, and BA.4/5 receptor-binding domains, whereas Omicron primary infections elicit B cells of narrow specificity up to 6 months after infection. Although most clinical antibodies hav</pubmed_abstract><journal>Science (New York, N.Y.)</journal><pubmed_title>Imprinted antibody responses against SARS-CoV-2 Omicron sublineages.</pubmed_title><pmcid>PMC12945441</pmcid><funding_grant_id>S10 OD023476</funding_grant_id><funding_grant_id>DP1 AI158186</funding_grant_id><funding_grant_id>R01 AI163019</funding_grant_id><funding_grant_id>75N93022C00036</funding_grant_id><pubmed_authors>Rajesh A</pubmed_authors><pubmed_authors>Franko NM</pubmed_authors><pubmed_authors>Montiel-Ruiz M</pubmed_authors><pubmed_authors>Guarino B</pubmed_authors><pubmed_authors>Giannini O</pubmed_authors><pubmed_authors>di Iulio J</pubmed_authors><pubmed_authors>Abdelnabi R</pubmed_authors><pubmed_authors>Ceschi A</pubmed_authors><pubmed_authors>Schnell G</pubmed_authors><pubmed_authors>Park YJ</pubmed_authors><pubmed_authors>Corti D</pubmed_authors><pubmed_authors>Soriaga L</pubmed_authors><pubmed_authors>Sprouse KR</pubmed_authors><pubmed_authors>Stewart C</pubmed_authors><pubmed_authors>Addetia A</pubmed_authors><pubmed_authors>Bowen JE</pubmed_authors><pubmed_authors>Benigni F</pubmed_authors><pubmed_authors>Bassi J</pubmed_authors><pubmed_authors>Ferrari P</pubmed_authors><pubmed_authors>Logue JK</pubmed_authors><pubmed_authors>Schmid MA</pubmed_authors><pubmed_authors>Pizzuto MS</pubmed_authors><pubmed_authors>Noack J</pubmed_authors><pubmed_authors>Whelan SPJ</pubmed_authors><pubmed_authors>De Marco A</pubmed_authors><pubmed_authors>Dang HV</pubmed_authors><pubmed_authors>Hauser K</pubmed_authors><pubmed_authors>Neyts J</pubmed_authors><pubmed_authors>Pinto D</pubmed_authors><pubmed_authors>Lanzavecchia A</pubmed_authors><pubmed_authors>Piccoli L</pubmed_authors><pubmed_authors>Bourhy H</pubmed_authors><pubmed_authors>Virgin HW</pubmed_authors><pubmed_authors>Rivera W</pubmed_authors><pubmed_authors>Silacci-Fregni C</pubmed_authors><pubmed_authors>Kergoat L</pubmed_authors><pubmed_authors>Farhat N</pubmed_authors><pubmed_authors>Kaiser H</pubmed_authors><pubmed_authors>de Melo GD</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Janer J</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors><pubmed_authors>Chu HY</pubmed_authors><pubmed_authors>Purcell LA</pubmed_authors><pubmed_authors>Veesler D</pubmed_authors><pubmed_authors>Lempp FA</pubmed_authors><pubmed_authors>Walls AC</pubmed_authors><pubmed_authors>Snell G</pubmed_authors><pubmed_authors>Zatta F</pubmed_authors><pubmed_authors>Saliba C</pubmed_authors><pubmed_authors>Maes P</pubmed_authors><pubmed_authors>Giurdanella M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Imprinted antibody responses against SARS-CoV-2 Omicron sublineages.</name><description>Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron sublineages carry distinct spike mutations resulting in escape from antibodies induced by previous infection or vaccination. We show that hybrid immunity or vaccine boosters elicit plasma-neutralizing antibodies against Omicron BA.1, BA.2, BA.2.12.1, and BA.4/5, and that breakthrough infections, but not vaccination alone, induce neutralizing antibodies in the nasal mucosa. Consistent with immunological imprinting, most antibodies derived from memory B cells or plasma cells of Omicron breakthrough cases cross-react with the Wuhan-Hu-1, BA.1, BA.2, and BA.4/5 receptor-binding domains, whereas Omicron primary infections elicit B cells of narrow specificity up to 6 months after infection. Although most clinical antibodies hav</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-07-16T21:53:59Z</modification><creation>2026-07-10T03:15:40.52Z</creation></dates><accession>S-EPMC12945441</accession><cross_references><pubmed>36264829</pubmed><doi>10.1126/science.adc9127</doi></cross_references></HashMap>