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Adults with Trisomy 21 Have Differential Antibody Responses to Influenza A
Down syndrome is caused by an extra copy of chromosome 21. In the past two decades, the life expectancy of individuals with Down syndrome has significantly increased from early 20s to early 60s, creating a population of individuals of which little is known about how well they are protected against i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324516/ https://www.ncbi.nlm.nih.gov/pubmed/35891309 http://dx.doi.org/10.3390/vaccines10071145 |
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author | James, Stephanie Haight, Robert C. Hanna, Cassandra Furton, Lindsey |
author_facet | James, Stephanie Haight, Robert C. Hanna, Cassandra Furton, Lindsey |
author_sort | James, Stephanie |
collection | PubMed |
description | Down syndrome is caused by an extra copy of chromosome 21. In the past two decades, the life expectancy of individuals with Down syndrome has significantly increased from early 20s to early 60s, creating a population of individuals of which little is known about how well they are protected against infectious disease. The goal of this work is to better understand if adults with Down syndrome are well protected against influenza following vaccination. We obtained plasma samples from 18 adults (average age = 31yo) with Down syndrome and 17 age/gender-matched disomic individuals, all vaccinated against influenza. Antibody concentration to influenza A was measured using ELISA and antibody titers were measured using a hemagglutinin inhibition assay. Statistical analysis was performed using Stata Statistical Software. Adults with Down syndrome had a significantly increased concentration of antibodies to a mixture of influenza A viral proteins; however, they had a significantly decreased titer to the Influenza A/Hong Kong compared to disomic controls. These findings suggest that more vigorous studies of B- and T-cell function in adults with Down syndrome with respect to influenza vaccination are warranted, and that this population may benefit from a high-dose influenza vaccine. |
format | Online Article Text |
id | pubmed-9324516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93245162022-07-27 Adults with Trisomy 21 Have Differential Antibody Responses to Influenza A James, Stephanie Haight, Robert C. Hanna, Cassandra Furton, Lindsey Vaccines (Basel) Brief Report Down syndrome is caused by an extra copy of chromosome 21. In the past two decades, the life expectancy of individuals with Down syndrome has significantly increased from early 20s to early 60s, creating a population of individuals of which little is known about how well they are protected against infectious disease. The goal of this work is to better understand if adults with Down syndrome are well protected against influenza following vaccination. We obtained plasma samples from 18 adults (average age = 31yo) with Down syndrome and 17 age/gender-matched disomic individuals, all vaccinated against influenza. Antibody concentration to influenza A was measured using ELISA and antibody titers were measured using a hemagglutinin inhibition assay. Statistical analysis was performed using Stata Statistical Software. Adults with Down syndrome had a significantly increased concentration of antibodies to a mixture of influenza A viral proteins; however, they had a significantly decreased titer to the Influenza A/Hong Kong compared to disomic controls. These findings suggest that more vigorous studies of B- and T-cell function in adults with Down syndrome with respect to influenza vaccination are warranted, and that this population may benefit from a high-dose influenza vaccine. MDPI 2022-07-19 /pmc/articles/PMC9324516/ /pubmed/35891309 http://dx.doi.org/10.3390/vaccines10071145 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Brief Report James, Stephanie Haight, Robert C. Hanna, Cassandra Furton, Lindsey Adults with Trisomy 21 Have Differential Antibody Responses to Influenza A |
title | Adults with Trisomy 21 Have Differential Antibody Responses to Influenza A |
title_full | Adults with Trisomy 21 Have Differential Antibody Responses to Influenza A |
title_fullStr | Adults with Trisomy 21 Have Differential Antibody Responses to Influenza A |
title_full_unstemmed | Adults with Trisomy 21 Have Differential Antibody Responses to Influenza A |
title_short | Adults with Trisomy 21 Have Differential Antibody Responses to Influenza A |
title_sort | adults with trisomy 21 have differential antibody responses to influenza a |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9324516/ https://www.ncbi.nlm.nih.gov/pubmed/35891309 http://dx.doi.org/10.3390/vaccines10071145 |
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