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T and B Cell Receptor Immune Repertoire Analysis using Next-generation Sequencing
Published on: January 12, 2021
Naive and Memory B Cell BCR Repertoires in Individuals Immunized with an Inactivated SARS-CoV-2 Vaccine
Renato Kaylan Alves de Oliveira França1,2, Pedro Henrique Aragão Barros1,3, Jacyelle Medeiros Silva1
1Department of Cellular Biology, Institute of Biological Science, University of Brasília, Brasilia 70910-900, DF, Brazil.
This study analyzed B-cell memory after CoronaVac vaccination, finding it elicits antibodies similar to neutralizing ones. Immunization is key for generating convergent antibodies against viral infections like COVID-19.
Area of Science:
- Immunology
- Vaccinology
- Molecular Biology
Background:
- The COVID-19 pandemic necessitated rapid vaccine development, including inactivated virus vaccines like CoronaVac.
- CoronaVac showed limitations against emerging SARS-CoV-2 variants.
- Memory B-cells are crucial for adaptive immunity and producing neutralizing antibodies.
Purpose of the Study:
- To investigate the B-cell memory repertoire following two doses of the CoronaVac vaccine.
- To understand the characteristics of antibodies generated by CoronaVac.
Main Methods:
- Isolation of memory B-cells from vaccinated and pre-pandemic individuals.
- In vitro stimulation of B-cells.
- High-throughput sequencing of the Heavy Chain Variable (VH) repertoire.
Main Results:
- A shift in the VH repertoire was observed, with increased HCDR3 length and specific VH gene enrichment for IgA and IgG B-cell receptors (BCRs).
- Significant expansion of IgA-specific clonal populations and shared IgA VH sequences were found in vaccinated individuals.
- Vaccinee antibody sequences showed convergence with known SARS-CoV-2 neutralizing antibodies.
Conclusions:
- CoronaVac elicits antibodies with characteristics of neutralizing antibodies, supporting its protective role.
- Immunization is vital for generating convergent antibodies, enhancing the antiviral immune response.
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