SARS-CoV-2 mRNA Vaccines Foster Potent Antigen-Specific Germinal Center Responses Associated with Neutralizing Antibody Generation
ABSTRACT: The deployment of effective vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is critical to eradicate the coronavirus disease 2019 (COVID-19) pandemic. Many licensed vaccines confer protection by inducing long-lived plasma cells (LLPCs) and memory B cells (MBCs...
- Autores:
-
Castaño Monsalve, Diana María
Lederer, Katlyn
Gómez Atria, Daniela
Oguin III, Thomas H.
Sidney, Wang
Tomaz B., Manzoni
Muramatsu, Hiromi
Hogan, Michael J.
Amanat, Fatima
Cherubin, Patrick
Lundgreen, Kendall A.
Tam, Ying K
Steven H.Y., Fan
Laurence C., Eisenlohr
Maillard, Ivan
Weissman, Drew
Bates, Paul
Krammer, Florian
Sempowsk, Gregory D.
Pardi, Norbert
Locci, Michela
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2020
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/42018
- Acceso en línea:
- https://hdl.handle.net/10495/42018
- Palabra clave:
- COVID-19
Anticuerpos Neutralizantes
Antibodies, Neutralizing
Antígenos Virales
Antigens, Viral
Linfocitos B
B-Lymphocytes
Células Cultivadas
Cells, Cultured
Centro Germinal
Germinal Center
Vacunas de ARNm
mRNA Vaccines
Epítopos
Epitopes
Activación de Linfocitos
Lymphocyte Activation
SARS-CoV-2
https://id.nlm.nih.gov/mesh/D000086382
https://id.nlm.nih.gov/mesh/D057134
https://id.nlm.nih.gov/mesh/D000956
https://id.nlm.nih.gov/mesh/D001402
https://id.nlm.nih.gov/mesh/D002478
https://id.nlm.nih.gov/mesh/D018858
https://id.nlm.nih.gov/mesh/D000087503
https://id.nlm.nih.gov/mesh/D000939
https://id.nlm.nih.gov/mesh/D008213
https://id.nlm.nih.gov/mesh/D000086402
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-nd/4.0/
| Summary: | ABSTRACT: The deployment of effective vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is critical to eradicate the coronavirus disease 2019 (COVID-19) pandemic. Many licensed vaccines confer protection by inducing long-lived plasma cells (LLPCs) and memory B cells (MBCs), cell types canonically generated during germinal center (GC) reactions. Here, we directly compared two vaccine platforms—mRNA vaccines and a recombinant protein formulated with an MF59-like adjuvant—looking for their abilities to quantitatively and qualitatively shape SARS-CoV-2-specific primary GC responses over time. We demonstrated that a single immunization with SARS-CoV-2 mRNA, but not with the recombinant protein vaccine, elicited potent SARS-CoV-2-specific GC B and T follicular helper (Tfh) cell responses as well as LLPCs and MBCs. Importantly, GC responses strongly correlated with neutralizing antibody production. mRNA vaccines more efficiently induced key regulators of the Tfh cell program and influenced the functional properties of Tfh cells. Overall, this study identifies SARS-CoV-2 mRNA vaccines as strong candidates for promoting robust GC-derived immune responses. |
|---|
