Salivary antibodies induced by BA.4/BA.5-convalescence or bivalent booster Immunoglobulin vaccination protect against novel SARS-COV-2 variants of concern

ABSTRACT Currently, SARS-CoV-2 Omicron BA.5 subvariants BF.7 and BQ.1.1 are rapidly emerging worldwide. To evaluate the SARS-CoV-2-neutralizing capacity of sera and saliva from triple vaccinated individuals, either boosted with an adapted bivalent COVID-19 vaccine or recovered from BA.4/BA.5 infecti...

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Main Authors: Gabriel Diem, Stefanie Dichtl, Viktoria Zaderer, Cornelia Lass-Flörl, Markus Reindl, Gaia Lupoli, Christopher Dächert, Maximilian Muenchhoff, Alexander Graf, Helmut Blum, Oliver T. Keppler, Doris Wilflingseder, Wilfried Posch
Format: Article
Language:English
Published: American Society for Microbiology 2023-10-01
Series:Microbiology Spectrum
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Online Access:https://journals.asm.org/doi/10.1128/spectrum.01793-23
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author Gabriel Diem
Stefanie Dichtl
Viktoria Zaderer
Cornelia Lass-Flörl
Markus Reindl
Gaia Lupoli
Christopher Dächert
Maximilian Muenchhoff
Alexander Graf
Helmut Blum
Oliver T. Keppler
Doris Wilflingseder
Wilfried Posch
author_facet Gabriel Diem
Stefanie Dichtl
Viktoria Zaderer
Cornelia Lass-Flörl
Markus Reindl
Gaia Lupoli
Christopher Dächert
Maximilian Muenchhoff
Alexander Graf
Helmut Blum
Oliver T. Keppler
Doris Wilflingseder
Wilfried Posch
author_sort Gabriel Diem
collection DOAJ
description ABSTRACT Currently, SARS-CoV-2 Omicron BA.5 subvariants BF.7 and BQ.1.1 are rapidly emerging worldwide. To evaluate the SARS-CoV-2-neutralizing capacity of sera and saliva from triple vaccinated individuals, either boosted with an adapted bivalent COVID-19 vaccine or recovered from BA.4/BA.5 infection, we analyzed the sensitivity of replication-competent SARS-CoV-2 Omicron subvariants BA.4/5, BQ.1.1 and BF.7 to neutralization. Analysis of SARS-CoV-2-specific IgGs and IgAs showed increased serum IgG titers in the vaccinated group, while the serum and salivary IgA levels were comparable. Similar and efficient serum neutralization against the ancestral strain of SARS-CoV-2 and Omicron BA.4/BA.5 was detected in both cohorts, but critically reduced for BQ.1.1 and BF.7. In contrast, salivary neutralization against BA.4/BA.5 was increased in the convalescent compared to the vaccinated group, while salivary neutralizing capacity against BQ.1.1 and BF.7 was comparable in these groups. Further, personalized protective effects studied in a human 3D respiratory model revealed the importance of salivary protection against different Omicron subvariants. IMPORTANCE In BA.4/BA.5-convalescent versus vaccinated groups, salivary neutralization capacity increased against SARS-CoV-2 Omicron BA.4/BA.5. In contrast, it neutralized novel Omicron subvariants BQ.1.1 and BF.7 similarly. Salivary protection against various Omicron subvariants was even more evident when tested in a personalized approach using highly differentiated respiratory human 3D models.
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spelling doaj.art-527ce07995894168987669d2926baf8e2023-10-17T13:04:36ZengAmerican Society for MicrobiologyMicrobiology Spectrum2165-04972023-10-0111510.1128/spectrum.01793-23Salivary antibodies induced by BA.4/BA.5-convalescence or bivalent booster Immunoglobulin vaccination protect against novel SARS-COV-2 variants of concernGabriel Diem0Stefanie Dichtl1Viktoria Zaderer2Cornelia Lass-Flörl3Markus Reindl4Gaia Lupoli5Christopher Dächert6Maximilian Muenchhoff7Alexander Graf8Helmut Blum9Oliver T. Keppler10Doris Wilflingseder11Wilfried Posch12Institute of Hygiene and Medical Microbiology, Medical University of Innsbruck , Innsbruck, AustriaInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck , Innsbruck, AustriaInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck , Innsbruck, AustriaInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck , Innsbruck, AustriaClinical Department of Neurology, Medical University of Innsbruck , Innsbruck, AustriaMax von Pettenkofer Institute and Gene Center, Virology, LMU München , Munich, GermanyMax von Pettenkofer Institute and Gene Center, Virology, LMU München , Munich, GermanyMax von Pettenkofer Institute and Gene Center, Virology, LMU München , Munich, GermanyLaboratory for Functional Genome Analysis, Gene Center, LMU München , Munich, GermanyLaboratory for Functional Genome Analysis, Gene Center, LMU München , Munich, GermanyMax von Pettenkofer Institute and Gene Center, Virology, LMU München , Munich, GermanyInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck , Innsbruck, AustriaInstitute of Hygiene and Medical Microbiology, Medical University of Innsbruck , Innsbruck, AustriaABSTRACT Currently, SARS-CoV-2 Omicron BA.5 subvariants BF.7 and BQ.1.1 are rapidly emerging worldwide. To evaluate the SARS-CoV-2-neutralizing capacity of sera and saliva from triple vaccinated individuals, either boosted with an adapted bivalent COVID-19 vaccine or recovered from BA.4/BA.5 infection, we analyzed the sensitivity of replication-competent SARS-CoV-2 Omicron subvariants BA.4/5, BQ.1.1 and BF.7 to neutralization. Analysis of SARS-CoV-2-specific IgGs and IgAs showed increased serum IgG titers in the vaccinated group, while the serum and salivary IgA levels were comparable. Similar and efficient serum neutralization against the ancestral strain of SARS-CoV-2 and Omicron BA.4/BA.5 was detected in both cohorts, but critically reduced for BQ.1.1 and BF.7. In contrast, salivary neutralization against BA.4/BA.5 was increased in the convalescent compared to the vaccinated group, while salivary neutralizing capacity against BQ.1.1 and BF.7 was comparable in these groups. Further, personalized protective effects studied in a human 3D respiratory model revealed the importance of salivary protection against different Omicron subvariants. IMPORTANCE In BA.4/BA.5-convalescent versus vaccinated groups, salivary neutralization capacity increased against SARS-CoV-2 Omicron BA.4/BA.5. In contrast, it neutralized novel Omicron subvariants BQ.1.1 and BF.7 similarly. Salivary protection against various Omicron subvariants was even more evident when tested in a personalized approach using highly differentiated respiratory human 3D models.https://journals.asm.org/doi/10.1128/spectrum.01793-23SARS-CoV-2variants of concernsalivary antibodiesOmicronvaccinationconvalescence
spellingShingle Gabriel Diem
Stefanie Dichtl
Viktoria Zaderer
Cornelia Lass-Flörl
Markus Reindl
Gaia Lupoli
Christopher Dächert
Maximilian Muenchhoff
Alexander Graf
Helmut Blum
Oliver T. Keppler
Doris Wilflingseder
Wilfried Posch
Salivary antibodies induced by BA.4/BA.5-convalescence or bivalent booster Immunoglobulin vaccination protect against novel SARS-COV-2 variants of concern
Microbiology Spectrum
SARS-CoV-2
variants of concern
salivary antibodies
Omicron
vaccination
convalescence
title Salivary antibodies induced by BA.4/BA.5-convalescence or bivalent booster Immunoglobulin vaccination protect against novel SARS-COV-2 variants of concern
title_full Salivary antibodies induced by BA.4/BA.5-convalescence or bivalent booster Immunoglobulin vaccination protect against novel SARS-COV-2 variants of concern
title_fullStr Salivary antibodies induced by BA.4/BA.5-convalescence or bivalent booster Immunoglobulin vaccination protect against novel SARS-COV-2 variants of concern
title_full_unstemmed Salivary antibodies induced by BA.4/BA.5-convalescence or bivalent booster Immunoglobulin vaccination protect against novel SARS-COV-2 variants of concern
title_short Salivary antibodies induced by BA.4/BA.5-convalescence or bivalent booster Immunoglobulin vaccination protect against novel SARS-COV-2 variants of concern
title_sort salivary antibodies induced by ba 4 ba 5 convalescence or bivalent booster immunoglobulin vaccination protect against novel sars cov 2 variants of concern
topic SARS-CoV-2
variants of concern
salivary antibodies
Omicron
vaccination
convalescence
url https://journals.asm.org/doi/10.1128/spectrum.01793-23
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