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Activation Dynamics and Immunoglobulin Evolution of Pre-existing and Newly Generated Human Memory B cell Responses to Influenza Hemagglutinin.
- Source :
-
Immunity (10747613) . Aug2019, Vol. 51 Issue 2, p398-398. 1p. - Publication Year :
- 2019
-
Abstract
- Vaccine-induced memory B cell responses to evolving viruses like influenza A involve activation of pre-existing immunity and generation of new responses. To define the contribution of these two types of responses, we analyzed the response to H7N9 vaccination in H7N9-naive adults. We performed comprehensive comparisons at the single-cell level of the kinetics, Ig repertoire, and activation phenotype of established pre-existing memory B cells recognizing conserved epitopes and the newly generated memory B cells directed toward H7 strain-specific epitopes. The recall response to conserved epitopes on H7 HA involved a transient expansion of memory B cells with little observed adaptation. However, the B cell response to newly encountered epitopes was phenotypically distinct and generated a sustained memory population that evolved and affinity matured months after vaccination. These findings establish clear differences between newly generated and pre-existing memory B cells, highlighting the challenges in achieving long-lasting, broad protection against an ever-evolving virus. • Newly generated memory B cells evolve and affinity mature over several months • Long-term pre-existing memory B cells evolve little upon re-vaccination • Newly generated memory B cells transiently become atypical, T-bethi CD21lo CD27− • T-betlo CD21hi CD27−, but not CD27+, resting memory B cells are maintained long-term Influenza vaccination occurs in the context of pre-existing immunity. Andrews et al. compare the pre-existing memory IgG B cell response recognizing conserved epitopes on influenza hemagglutinin with the newly generated response to strain-specific epitopes upon H7N9 vaccination. The differences in magnitude, phenotype, and affinity maturation between the two responses highlight the challenges in achieving long-lasting, broad protection against an ever-evolving virus. [ABSTRACT FROM AUTHOR]
- Subjects :
- *B cells
*MEMORY
*HEMAGGLUTININ
*INFLUENZA
*INFLUENZA vaccines
Subjects
Details
- Language :
- English
- ISSN :
- 10747613
- Volume :
- 51
- Issue :
- 2
- Database :
- Academic Search Index
- Journal :
- Immunity (10747613)
- Publication Type :
- Academic Journal
- Accession number :
- 138097581
- Full Text :
- https://doi.org/10.1016/j.immuni.2019.06.024