Structural serology of polyclonal antibody responses to mRNA-1273 and NVX-CoV2373 COVID-19 vaccines
2024

Study of Antibody Responses to COVID-19 Vaccines

Sample size: 20 publication 15 minutes Evidence: moderate

Author Information

Author(s): Bangaru Sandhya, Jackson Abigail M., Copps Jeffrey, Fernández-Quintero Monica L., Torres Jonathan L., Richey Sara T., Nogal Bartek, Sewall Leigh M., de la Peña Alba Torrents, Rehman Asma, Guebre-Xabier Mimi, Girard Bethany, Das Rituparna, Corbett-Helaire Kizzmekia S., Seder Robert A., Graham Barney S., Edwards Darin K., Patel Nita, Smith Gale, Ward Andrew B.

Primary Institution: The Scripps Research Institute

Hypothesis

How do mRNA-1273 and NVX-CoV2373 vaccines induce antibody responses?

Conclusion

Both mRNA-1273 and NVX-CoV2373 vaccines elicit diverse antibody responses, particularly targeting the NTD supersite, which is susceptible to variant mutations.

Supporting Evidence

  • Both vaccines induce diverse polyclonal antibody responses to the N-terminal domain and receptor-binding domain of the Spike protein.
  • NTD supersite antibodies were the most susceptible to variant mutations compared to other specificities.
  • High-resolution cryo-EMPEM studies revealed extensive pAb responses to and around the supersite.

Takeaway

The study looked at how two COVID-19 vaccines make antibodies in people and found that they both create strong responses, especially to a specific part of the virus that can change.

Methodology

Electron microscopy-based polyclonal epitope mapping (EMPEM) was used to analyze serum from immunized non-human primates and clinical trial donors.

Limitations

The study primarily focused on two vaccines and may not represent responses to other COVID-19 vaccines.

Participant Demographics

The study involved non-human primates and clinical trial donors, including both male and female participants.

Digital Object Identifier (DOI)

10.1101/2024.12.11.628030

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