Immune response to SARS-CoV-2 variants of concern in vaccinated individuals

被引:0
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作者
Matthias Becker
Alex Dulovic
Daniel Junker
Natalia Ruetalo
Philipp D. Kaiser
Yudi T. Pinilla
Constanze Heinzel
Julia Haering
Bjoern Traenkle
Teresa R. Wagner
Mirjam Layer
Martin Mehrlaender
Valbona Mirakaj
Jana Held
Hannes Planatscher
Katja Schenke-Layland
Gérard Krause
Monika Strengert
Tamam Bakchoul
Karina Althaus
Rolf Fendel
Andrea Kreidenweiss
Michael Koeppen
Ulrich Rothbauer
Michael Schindler
Nicole Schneiderhan-Marra
机构
[1] NMI Natural and Medical Sciences Institute at the University of Tübingen,Institute for Medical Virology and Epidemiology
[2] University Hospital Tübingen,Institute of Tropical Medicine
[3] University of Tübingen,Pharmaceutical Biotechnology
[4] University of Tübingen,Department of Anaesthesiology and Intensive Care Medicine
[5] University Hospital Tübingen,German Center for Infection Research (DZIF)
[6] partner site Tübingen,Cluster of Excellence iFIT (EXC2180) “Image
[7] Signatope GmbH,Guided and Functionally Instructed Tumor Therapies”
[8] University of Tübingen,Department of Women’s Health, Research Institute for Women’s Health
[9] University of Tübingen,Department of Medicine/Cardiology, Cardiovascular Research Laboratories
[10] David Geffen School of Medicine at UCLA,TWINCORE GmbH, Centre for Experimental and Clinical Infection Research
[11] Helmholtz Centre for Infection Research,Institute for Clinical and Experimental Transfusion Medicine
[12] a joint venture of the Hannover Medical School and the Helmholtz Centre for Infection Research,undefined
[13] University Hospital Tübingen,undefined
来源
Nature Communications | / 12卷
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摘要
SARS-CoV-2 is evolving with mutations in the receptor binding domain (RBD) being of particular concern. It is important to know how much cross-protection is offered between strains following vaccination or infection. Here, we obtain serum and saliva samples from groups of vaccinated (Pfizer BNT-162b2), infected and uninfected individuals and characterize the antibody response to RBD mutant strains. Vaccinated individuals have a robust humoral response after the second dose and have high IgG antibody titers in the saliva. Antibody responses however show considerable differences in binding to RBD mutants of emerging variants of concern and substantial reduction in RBD binding and neutralization is observed against a patient-isolated South African variant. Taken together our data reinforce the importance of the second dose of Pfizer BNT-162b2 to acquire high levels of neutralizing antibodies and high antibody titers in saliva suggest that vaccinated individuals may have reduced transmission potential. Substantially reduced neutralization for the South African variant further highlights the importance of surveillance strategies to detect new variants and targeting these in future vaccines.
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