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High-Resolution Temporal Response Patterns to Influenza Vaccine Reveal a Distinct Human Plasma Cell Gene Signature
To identify sources of inter-subject variation in vaccine responses, we performed high-frequency sampling of human peripheral blood cells post-vaccination, followed by a novel systems biology analysis. Functional principal component analysis was used to examine time varying B cell vaccine responses....
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Published in: | Scientific reports 2013-07, Vol.3 (1), p.2327, Article 2327 |
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description | To identify sources of inter-subject variation in vaccine responses, we performed high-frequency sampling of human peripheral blood cells post-vaccination, followed by a novel systems biology analysis. Functional principal component analysis was used to examine time varying B cell vaccine responses. In subjects vaccinated within the previous three years, 90% of transcriptome variation was explained by a single subject-specific mathematical pattern. Within individual vaccine response patterns, a common subset of 742 genes was strongly correlated with migrating plasma cells. Of these, 366 genes were associated with human plasmablasts differentiating
in vitro
. Additionally, subject-specific temporal transcriptome patterns in peripheral blood mononuclear cells identified migration of myeloid/dendritic cell lineage cells one day after vaccination. Upstream analyses of transcriptome changes suggested both shared and subject-specific transcription groups underlying larger patterns. With robust statistical methods, time-varying response characteristics of individual subjects were effectively captured along with a shared plasma cell gene signature. |
doi_str_mv | 10.1038/srep02327 |
format | article |
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in vitro
. Additionally, subject-specific temporal transcriptome patterns in peripheral blood mononuclear cells identified migration of myeloid/dendritic cell lineage cells one day after vaccination. Upstream analyses of transcriptome changes suggested both shared and subject-specific transcription groups underlying larger patterns. With robust statistical methods, time-varying response characteristics of individual subjects were effectively captured along with a shared plasma cell gene signature.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep02327</identifier><identifier>PMID: 23900141</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/250/2152/1566/1571 ; 631/250/590/1883 ; 631/553/1833 ; 631/553/2701 ; B-Lymphocytes - drug effects ; B-Lymphocytes - immunology ; Blood Proteins - genetics ; Blood Proteins - immunology ; Cell lineage ; Cells, Cultured ; Dendritic cells ; Gene expression ; Gene Expression Regulation - drug effects ; Gene Expression Regulation - genetics ; Gene Expression Regulation - immunology ; Genes ; Humanities and Social Sciences ; Humans ; Immunization ; Influenza ; Influenza Vaccines - administration & dosage ; Influenza Vaccines - immunology ; Leukocytes (mononuclear) ; Lymphocytes B ; multidisciplinary ; Peripheral blood mononuclear cells ; Plasma cells ; Science ; Transcription ; Transcriptome - drug effects ; Transcriptome - immunology ; Vaccination ; Vaccines</subject><ispartof>Scientific reports, 2013-07, Vol.3 (1), p.2327, Article 2327</ispartof><rights>The Author(s) 2013</rights><rights>Copyright Nature Publishing Group Jul 2013</rights><rights>Copyright © 2013, Macmillan Publishers Limited. All rights reserved 2013 Macmillan Publishers Limited. All rights reserved</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-be75e0a50e74da4a6f64e7cdede18769fe115a8cbbf5ed6bfffd46d030a3a4a43</citedby><cites>FETCH-LOGICAL-c438t-be75e0a50e74da4a6f64e7cdede18769fe115a8cbbf5ed6bfffd46d030a3a4a43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1897440320/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1897440320?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23900141$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Henn, Alicia D.</creatorcontrib><creatorcontrib>Wu, Shuang</creatorcontrib><creatorcontrib>Qiu, Xing</creatorcontrib><creatorcontrib>Ruda, Melissa</creatorcontrib><creatorcontrib>Stover, Michael</creatorcontrib><creatorcontrib>Yang, Hongmei</creatorcontrib><creatorcontrib>Liu, Zhiping</creatorcontrib><creatorcontrib>Welle, Stephen L.</creatorcontrib><creatorcontrib>Holden-Wiltse, Jeanne</creatorcontrib><creatorcontrib>Wu, Hulin</creatorcontrib><creatorcontrib>Zand, Martin S.</creatorcontrib><title>High-Resolution Temporal Response Patterns to Influenza Vaccine Reveal a Distinct Human Plasma Cell Gene Signature</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>To identify sources of inter-subject variation in vaccine responses, we performed high-frequency sampling of human peripheral blood cells post-vaccination, followed by a novel systems biology analysis. Functional principal component analysis was used to examine time varying B cell vaccine responses. In subjects vaccinated within the previous three years, 90% of transcriptome variation was explained by a single subject-specific mathematical pattern. Within individual vaccine response patterns, a common subset of 742 genes was strongly correlated with migrating plasma cells. Of these, 366 genes were associated with human plasmablasts differentiating
in vitro
. Additionally, subject-specific temporal transcriptome patterns in peripheral blood mononuclear cells identified migration of myeloid/dendritic cell lineage cells one day after vaccination. Upstream analyses of transcriptome changes suggested both shared and subject-specific transcription groups underlying larger patterns. 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Functional principal component analysis was used to examine time varying B cell vaccine responses. In subjects vaccinated within the previous three years, 90% of transcriptome variation was explained by a single subject-specific mathematical pattern. Within individual vaccine response patterns, a common subset of 742 genes was strongly correlated with migrating plasma cells. Of these, 366 genes were associated with human plasmablasts differentiating
in vitro
. Additionally, subject-specific temporal transcriptome patterns in peripheral blood mononuclear cells identified migration of myeloid/dendritic cell lineage cells one day after vaccination. Upstream analyses of transcriptome changes suggested both shared and subject-specific transcription groups underlying larger patterns. With robust statistical methods, time-varying response characteristics of individual subjects were effectively captured along with a shared plasma cell gene signature.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>23900141</pmid><doi>10.1038/srep02327</doi><oa>free_for_read</oa></addata></record> |
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subjects | 631/250/2152/1566/1571 631/250/590/1883 631/553/1833 631/553/2701 B-Lymphocytes - drug effects B-Lymphocytes - immunology Blood Proteins - genetics Blood Proteins - immunology Cell lineage Cells, Cultured Dendritic cells Gene expression Gene Expression Regulation - drug effects Gene Expression Regulation - genetics Gene Expression Regulation - immunology Genes Humanities and Social Sciences Humans Immunization Influenza Influenza Vaccines - administration & dosage Influenza Vaccines - immunology Leukocytes (mononuclear) Lymphocytes B multidisciplinary Peripheral blood mononuclear cells Plasma cells Science Transcription Transcriptome - drug effects Transcriptome - immunology Vaccination Vaccines |
title | High-Resolution Temporal Response Patterns to Influenza Vaccine Reveal a Distinct Human Plasma Cell Gene Signature |
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