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Impaired memory B-cell recall responses in the elderly following recurrent influenza vaccination
Influenza is a highly contagious viral respiratory disease that affects million of people worldwide each year. Annual vaccination is recommended by the World Health Organization with the goal of reducing influenza severity and limiting transmission through elicitation of antibodies targeting the hem...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341655/ https://www.ncbi.nlm.nih.gov/pubmed/34351920 http://dx.doi.org/10.1371/journal.pone.0254421 |
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author | Abreu, Rodrigo B. Kirchenbaum, Greg A. Sautto, Giuseppe A. Clutter, Emily F. Ross, Ted M. |
author_facet | Abreu, Rodrigo B. Kirchenbaum, Greg A. Sautto, Giuseppe A. Clutter, Emily F. Ross, Ted M. |
author_sort | Abreu, Rodrigo B. |
collection | PubMed |
description | Influenza is a highly contagious viral respiratory disease that affects million of people worldwide each year. Annual vaccination is recommended by the World Health Organization with the goal of reducing influenza severity and limiting transmission through elicitation of antibodies targeting the hemagglutinin (HA) glycoprotein. The antibody response elicited by current seasonal influenza virus vaccines is predominantly strain-specific, but pre-existing influenza virus immunity can greatly impact the serological antibody response to vaccination. However, it remains unclear how B cell memory is shaped by recurrent annual vaccination over the course of multiple seasons, especially in high-risk elderly populations. Here, we systematically profiled the B cell response in young adult (18–34 year old) and elderly (65+ year old) vaccine recipients that received annual split inactivated influenza virus vaccination for 3 consecutive seasons. Specifically, the antibody serological and memory B-cell compartments were profiled for reactivity against current and historical influenza A virus strains. Moreover, multiparametric analysis and antibody landscape profiling revealed a transient increase in strain-specific antibodies in the elderly, but with an impaired recall response of pre-existing memory B-cells, plasmablast (PB) differentiation and long-lasting serological changes. This study thoroughly profiles and compares the immune response to recurrent influenza virus vaccination in young and elderly participants unveiling the pitfalls of current influenza virus vaccines in high-risk populations. |
format | Online Article Text |
id | pubmed-8341655 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-83416552021-08-06 Impaired memory B-cell recall responses in the elderly following recurrent influenza vaccination Abreu, Rodrigo B. Kirchenbaum, Greg A. Sautto, Giuseppe A. Clutter, Emily F. Ross, Ted M. PLoS One Research Article Influenza is a highly contagious viral respiratory disease that affects million of people worldwide each year. Annual vaccination is recommended by the World Health Organization with the goal of reducing influenza severity and limiting transmission through elicitation of antibodies targeting the hemagglutinin (HA) glycoprotein. The antibody response elicited by current seasonal influenza virus vaccines is predominantly strain-specific, but pre-existing influenza virus immunity can greatly impact the serological antibody response to vaccination. However, it remains unclear how B cell memory is shaped by recurrent annual vaccination over the course of multiple seasons, especially in high-risk elderly populations. Here, we systematically profiled the B cell response in young adult (18–34 year old) and elderly (65+ year old) vaccine recipients that received annual split inactivated influenza virus vaccination for 3 consecutive seasons. Specifically, the antibody serological and memory B-cell compartments were profiled for reactivity against current and historical influenza A virus strains. Moreover, multiparametric analysis and antibody landscape profiling revealed a transient increase in strain-specific antibodies in the elderly, but with an impaired recall response of pre-existing memory B-cells, plasmablast (PB) differentiation and long-lasting serological changes. This study thoroughly profiles and compares the immune response to recurrent influenza virus vaccination in young and elderly participants unveiling the pitfalls of current influenza virus vaccines in high-risk populations. Public Library of Science 2021-08-05 /pmc/articles/PMC8341655/ /pubmed/34351920 http://dx.doi.org/10.1371/journal.pone.0254421 Text en © 2021 Abreu et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Abreu, Rodrigo B. Kirchenbaum, Greg A. Sautto, Giuseppe A. Clutter, Emily F. Ross, Ted M. Impaired memory B-cell recall responses in the elderly following recurrent influenza vaccination |
title | Impaired memory B-cell recall responses in the elderly following recurrent influenza vaccination |
title_full | Impaired memory B-cell recall responses in the elderly following recurrent influenza vaccination |
title_fullStr | Impaired memory B-cell recall responses in the elderly following recurrent influenza vaccination |
title_full_unstemmed | Impaired memory B-cell recall responses in the elderly following recurrent influenza vaccination |
title_short | Impaired memory B-cell recall responses in the elderly following recurrent influenza vaccination |
title_sort | impaired memory b-cell recall responses in the elderly following recurrent influenza vaccination |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8341655/ https://www.ncbi.nlm.nih.gov/pubmed/34351920 http://dx.doi.org/10.1371/journal.pone.0254421 |
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