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Antibody evolution to SARS-CoV-2 after single-dose Ad26.COV2.S vaccine
Alice Cho; Frauke Muecksch; Zijun Wang; Tarek Ben Tanfous; Justin DaSilva; Raphael Raspe; Brianna Johnson; Eva Bednarski; Victor Ramos; Dennis Schaefer-Babajew; Irina Shimeliovich; Juan Dizon; Kai-Hui Yao; Fabian Schmidt; Katrina G Millard; Martina Turroja; Mila Jankovic; Thiago Y Oliveira; Anna Gazumyan; Christian Gaebler; Marina Caskey; Theodora Hatziioannou; Paul D Bieniasz; Michel C Nussenzweig.
Affiliation
  • Alice Cho; Rockefeller University
  • Frauke Muecksch; The Rockefeller University
  • Zijun Wang; The Rockefeller University
  • Tarek Ben Tanfous; The Rockefeller University
  • Justin DaSilva; The Rockefeller University
  • Raphael Raspe; The Rockefeller University
  • Brianna Johnson; The Rockefeller University
  • Eva Bednarski; The Rockefeller University
  • Victor Ramos; The Rockefeller University
  • Dennis Schaefer-Babajew; The Rockefeller University
  • Irina Shimeliovich; The Rockefeller University
  • Juan Dizon; The Rockefeller University
  • Kai-Hui Yao; The Rockefeller University
  • Fabian Schmidt; The Rockefeller University
  • Katrina G Millard; The Rockefeller University
  • Martina Turroja; The Rockefeller University
  • Mila Jankovic; The Rockefeller University
  • Thiago Y Oliveira; The Rockefeller University
  • Anna Gazumyan; The Rockefeller University
  • Christian Gaebler; The Rockefeller University
  • Marina Caskey; The Rockefeller University
  • Theodora Hatziioannou; The Rockefeller University
  • Paul D Bieniasz; The Rockefeller University
  • Michel C Nussenzweig; The Rockefeller University
Preprint in English | bioRxiv | ID: ppbiorxiv-486548
ABSTRACT
The single dose Ad.26.COV.2 (Janssen) vaccine elicits lower levels of neutralizing antibodies and shows more limited efficacy in protection against infection than either of the available mRNA vaccines. In addition, the Ad.26.COV.2 has been less effective in protection against severe disease during the Omicron surge. Here, we examined the memory B cell response to single dose Ad.26.COV.2 vaccination. Compared to mRNA vaccines, Ad.26.COV.2 recipients had significantly lower numbers of RBD-specific memory B cells 1.5 or 6 months after vaccination. Memory antibodies elicited by both vaccine types show comparable neutralizing potency against SARS-CoV-2 and Delta. However, the number of memory cells producing Omicron neutralizing antibodies was somewhat lower after Ad.26.COV.2 than mRNA vaccination. The data help explain why boosting Ad.26.COV.2 vaccine recipients with mRNA vaccines is effective, and why the Janssen vaccine appears to have been less protective against severe disease during the Omicron surge than the mRNA vaccine. One-Sentence SummaryAd.26.COV.2 vaccine results in lower quantity but comparable quality of protective memory B cells compared to mRNA vaccines.
License
cc_by_nc_nd
Full text: Available Collection: Preprints Database: bioRxiv Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: bioRxiv Language: English Year: 2022 Document type: Preprint
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