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Published on: June 5, 2021
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.
Durable immunity against SARS-CoV-2 may be provided by memory B cells (MBCs), even if antibody levels decrease. Most COVID-19 patients develop these S-RBD-specific MBCs, indicating lasting B cell protection after infection.
Area of Science:
- Immunology
- Virology
- Infectious Diseases
Background:
- Antibody levels against SARS-CoV-2 wane over time post-infection.
- This waning immunity raises concerns about the durability of humoral immunity and potential reinfection risk.
- Memory B cells (MBCs) are crucial for long-term immunity and may persist even when antibody titers decline.
Purpose of the Study:
- To investigate the presence and characteristics of SARS-CoV-2-specific memory B cells (MBCs) in individuals recovering from COVID-19.
- To determine if MBCs contribute to durable humoral immunity following SARS-CoV-2 infection.
- To compare MBC responses in patients with mild versus moderate-to-severe COVID-19.
Main Methods:
- Multidimensional flow cytometry was used to analyze S protein receptor binding domain-specific (S-RBD-specific) MBCs.
- Cohorts included ambulatory patients with mild COVID-19 (n=7) and hospitalized patients with moderate-to-severe disease (n=7).
- Analysis was performed at a median of 54 days post-symptom onset.
Main Results:
- S-RBD-specific class-switched MBCs were detected in 13 out of 14 participants.
- Resting MBCs (rMBCs) constituted the majority of S-RBD-specific MBCs.
- FCRL5 upregulation on rMBCs was more pronounced after mild infection compared to severe infection.
Conclusions:
- Most individuals infected with SARS-CoV-2 develop S-RBD-specific, class-switched resting MBCs.
- These MBCs resemble those induced by vaccination against other pathogens, suggesting durable B cell-mediated immunity.
- The findings provide evidence for lasting humoral immunity against SARS-CoV-2 following both mild and severe disease.
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