| Literature DB >> 34035301 |
Matthias Becker1, Alex Dulovic1, Daniel Junker1, Natalia Ruetalo2, Philipp D Kaiser1, Yudi T Pinilla3, Constanze Heinzel3, Julia Haering1, Bjoern Traenkle1, Teresa R Wagner1,4, Mirjam Layer2, Martin Mehrlaender5, Valbona Mirakaj5, Jana Held3,6, Hannes Planatscher7, Katja Schenke-Layland1,8,9,10, Gérard Krause11,12, Monika Strengert11,12, Tamam Bakchoul13, Karina Althaus13, Rolf Fendel3,6, Andrea Kreidenweiss3,6, Michael Koeppen5, Ulrich Rothbauer14,15, Michael Schindler16, Nicole Schneiderhan-Marra17.
Abstract
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.Entities:
Year: 2021 PMID: 34035301 DOI: 10.1038/s41467-021-23473-6
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919