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Durable SARS-CoV-2 B cell immunity after mild or severe disease
Clinton O Ogega1, Nicole E Skinner1, Paul W Blair1
1Division of Infectious Diseases, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Medrxiv : the Preprint Server for Health Sciences
|November 3, 2020
Summary
SARS-CoV-2 infection induces durable B cell immunity. Memory B cells (MBC) persist after antibody levels decline, suggesting long-term protection against COVID-19.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- Waning SARS-CoV-2 antibody levels raise concerns about durable humoral immunity and reinfection risk.
- Memory B cells (MBC) are crucial for long-term immunity, even if antibody titers decrease.
Approach:
- Analyzed S protein receptor binding domain (S-RBD)-specific MBC in mild and severe COVID-19 patients using multi-dimensional flow cytometry.
- Assessed MBC phenotype and frequency at a median of 54 days post-symptom onset.
Key Points:
- S-RBD-specific class-switched MBC were detected in most participants, including those with low antibody levels.
- Resting MBC (rMBC) constituted the majority of S-RBD-specific MBC.
- FCRL5, a marker of functional memory, was highly expressed on S-RBD-specific rMBC.
Conclusions:
- Most SARS-CoV-2 infected individuals develop durable B cell-mediated immunity.
- The identified MBC resemble those induced by effective vaccination, indicating long-term protection potential.
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