<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Martin V</submitter><funding>Medical Research Council</funding><funding>Biotechnology and Biological Sciences Research Council</funding><pagination>20140237</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4528414</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>370(1676)</volume><pubmed_abstract>Older people are more susceptible to infection, less responsive to vaccination and have a more inflammatory immune environment. Using spectratype analysis, we have previously shown that the B-cell repertoire of older people shows evidence of inappropriate clonal expansions in the absence of challenge, and that this loss of B-cell diversity correlates with poor health. Studies on response to vaccination, using both spectratyping and high-throughput sequencing of the repertoire, indicate that older responses to challenge are lacking in magnitude and/or delayed significantly. Also that some of the biologically significant differences may be in different classes of antibody. We have also previously shown that normal young B-cell repertoires can vary between different phenotypic subsets of B ce</pubmed_abstract><journal>Philosophical transactions of the Royal Society of London. Series B, Biological sciences</journal><pubmed_title>Ageing of the B-cell repertoire.</pubmed_title><pmcid>PMC4528414</pmcid><funding_grant_id>886421</funding_grant_id><funding_grant_id>MR/L01257X/1</funding_grant_id><funding_grant_id>BB/G017190/1</funding_grant_id><pubmed_authors>Martin V</pubmed_authors><pubmed_authors>Kipling D</pubmed_authors><pubmed_authors>Dunn-Walters D</pubmed_authors><pubmed_authors>Bryan Wu YC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ageing of the B-cell repertoire.</name><description>Older people are more susceptible to infection, less responsive to vaccination and have a more inflammatory immune environment. Using spectratype analysis, we have previously shown that the B-cell repertoire of older people shows evidence of inappropriate clonal expansions in the absence of challenge, and that this loss of B-cell diversity correlates with poor health. Studies on response to vaccination, using both spectratyping and high-throughput sequencing of the repertoire, indicate that older responses to challenge are lacking in magnitude and/or delayed significantly. Also that some of the biologically significant differences may be in different classes of antibody. We have also previously shown that normal young B-cell repertoires can vary between different phenotypic subsets of B ce</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Sep</publication><modification>2025-04-04T21:25:28.796Z</modification><creation>2019-03-26T22:39:15Z</creation></dates><accession>S-EPMC4528414</accession><cross_references><pubmed>26194751</pubmed><doi>10.1098/rstb.2014.0237</doi></cross_references></HashMap>