Immunogenic dendritic cells primed by social defeat enhance adaptive immunity to influenza A virus.
Identifieur interne : 000678 ( PubMed/Corpus ); précédent : 000677; suivant : 000679Immunogenic dendritic cells primed by social defeat enhance adaptive immunity to influenza A virus.
Auteurs : Nicole D. Powell ; Jacqueline W. Mays ; Michael T. Bailey ; Mark L. Hanke ; John F. SheridanSource :
- Brain, behavior, and immunity [ 1090-2139 ] ; 2011.
English descriptors
- KwdEn :
- Adaptive Immunity (immunology), Animals, Antigens, Viral (immunology), CD11 Antigens (immunology), CD8-Positive T-Lymphocytes (immunology), Cell Count, Competitive Behavior (physiology), Dendritic Cells (immunology), Epitopes (immunology), Flow Cytometry, Immunologic Memory, Influenza A virus (immunology), Interferon-alpha (biosynthesis), Interferon-gamma (biosynthesis), Male, Mice, Mice, Inbred C57BL, Reverse Transcriptase Polymerase Chain Reaction, Social Dominance, Social Environment, Stress, Psychological (immunology).
- MESH :
- chemical , biosynthesis : Interferon-alpha, Interferon-gamma.
- chemical , immunology : Antigens, Viral, CD11 Antigens, Epitopes.
- immunology : Adaptive Immunity, CD8-Positive T-Lymphocytes, Dendritic Cells, Influenza A virus, Stress, Psychological.
- physiology : Competitive Behavior.
- Animals, Cell Count, Flow Cytometry, Immunologic Memory, Male, Mice, Mice, Inbred C57BL, Reverse Transcriptase Polymerase Chain Reaction, Social Dominance, Social Environment.
Abstract
Dendritic cells (DCs) sample their surrounding microenvironment and consequently send immunogenic or regulatory signals to T cells during DC/T cell interactions, shaping the primary adaptive immune response to infection. The microenvironment resulting from repeated social defeat increases DC co-stimulatory molecule expression and primes DCs for enhanced cytokine responses in vitro. In this study, we show that social disruption stress (SDR) results in the generation of immunogenic DCs, capable of conferring enhanced adaptive immunity to influenza A/PR/8/34 infection. Mice infected with influenza A/PR/8/34 virus 24 h after the adoptive transfer of DCs from SDR mice had significantly increased numbers of D(b)NP(366-74)CD8(+) T cells, increased IFN-γ and IFN-α mRNA, and decreased influenza M1 mRNA expression in the lung during the peak primary response (9 days post-infection), compared to mice that received DCs from naïve mice. These data demonstrate that repeated social defeat is a significant environmental influence on immunogenic DC activation and function.
DOI: 10.1016/j.bbi.2010.07.243
PubMed: 20656014
Links to Exploration step
pubmed:20656014Le document en format XML
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Hanke</name></author><author><name sortKey="Sheridan, John F" sort="Sheridan, John F" uniqKey="Sheridan J" first="John F" last="Sheridan">John F. Sheridan</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2011">2011</date><idno type="RBID">pubmed:20656014</idno><idno type="pmid">20656014</idno><idno type="doi">10.1016/j.bbi.2010.07.243</idno><idno type="wicri:Area/PubMed/Corpus">000678</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000678</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Immunogenic dendritic cells primed by social defeat enhance adaptive immunity to influenza A virus.</title><author><name sortKey="Powell, Nicole D" sort="Powell, Nicole D" uniqKey="Powell N" first="Nicole D" last="Powell">Nicole D. Powell</name><affiliation><nlm:affiliation>Section of Oral Biology, College of Dentistry, The Ohio State University, Columbus, OH, USA. Nicole.Powell@osumc.edu</nlm:affiliation></affiliation></author><author><name sortKey="Mays, Jacqueline W" sort="Mays, Jacqueline W" uniqKey="Mays J" first="Jacqueline W" last="Mays">Jacqueline W. Mays</name></author><author><name sortKey="Bailey, Michael T" sort="Bailey, Michael T" uniqKey="Bailey M" first="Michael T" last="Bailey">Michael T. Bailey</name></author><author><name sortKey="Hanke, Mark L" sort="Hanke, Mark L" uniqKey="Hanke M" first="Mark L" last="Hanke">Mark L. Hanke</name></author><author><name sortKey="Sheridan, John F" sort="Sheridan, John F" uniqKey="Sheridan J" first="John F" last="Sheridan">John F. Sheridan</name></author></analytic><series><title level="j">Brain, behavior, and immunity</title><idno type="eISSN">1090-2139</idno><imprint><date when="2011" type="published">2011</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adaptive Immunity (immunology)</term><term>Animals</term><term>Antigens, Viral (immunology)</term><term>CD11 Antigens (immunology)</term><term>CD8-Positive T-Lymphocytes (immunology)</term><term>Cell Count</term><term>Competitive Behavior (physiology)</term><term>Dendritic Cells (immunology)</term><term>Epitopes (immunology)</term><term>Flow Cytometry</term><term>Immunologic Memory</term><term>Influenza A virus (immunology)</term><term>Interferon-alpha (biosynthesis)</term><term>Interferon-gamma (biosynthesis)</term><term>Male</term><term>Mice</term><term>Mice, Inbred C57BL</term><term>Reverse Transcriptase Polymerase Chain Reaction</term><term>Social Dominance</term><term>Social Environment</term><term>Stress, Psychological (immunology)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="biosynthesis" xml:lang="en"><term>Interferon-alpha</term><term>Interferon-gamma</term></keywords><keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en"><term>Antigens, Viral</term><term>CD11 Antigens</term><term>Epitopes</term></keywords><keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>Adaptive Immunity</term><term>CD8-Positive T-Lymphocytes</term><term>Dendritic Cells</term><term>Influenza A virus</term><term>Stress, Psychological</term></keywords><keywords scheme="MESH" qualifier="physiology" xml:lang="en"><term>Competitive Behavior</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Cell Count</term><term>Flow Cytometry</term><term>Immunologic Memory</term><term>Male</term><term>Mice</term><term>Mice, Inbred C57BL</term><term>Reverse Transcriptase Polymerase Chain Reaction</term><term>Social Dominance</term><term>Social Environment</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Dendritic cells (DCs) sample their surrounding microenvironment and consequently send immunogenic or regulatory signals to T cells during DC/T cell interactions, shaping the primary adaptive immune response to infection. The microenvironment resulting from repeated social defeat increases DC co-stimulatory molecule expression and primes DCs for enhanced cytokine responses in vitro. In this study, we show that social disruption stress (SDR) results in the generation of immunogenic DCs, capable of conferring enhanced adaptive immunity to influenza A/PR/8/34 infection. Mice infected with influenza A/PR/8/34 virus 24 h after the adoptive transfer of DCs from SDR mice had significantly increased numbers of D(b)NP(366-74)CD8(+) T cells, increased IFN-γ and IFN-α mRNA, and decreased influenza M1 mRNA expression in the lung during the peak primary response (9 days post-infection), compared to mice that received DCs from naïve mice. These data demonstrate that repeated social defeat is a significant environmental influence on immunogenic DC activation and function.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">20656014</PMID><DateCompleted><Year>2011</Year><Month>03</Month><Day>10</Day></DateCompleted><DateRevised><Year>2018</Year><Month>11</Month><Day>13</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1090-2139</ISSN><JournalIssue CitedMedium="Internet"><Volume>25</Volume><Issue>1</Issue><PubDate><Year>2011</Year><Month>Jan</Month></PubDate></JournalIssue><Title>Brain, behavior, and immunity</Title><ISOAbbreviation>Brain Behav. Immun.</ISOAbbreviation></Journal><ArticleTitle>Immunogenic dendritic cells primed by social defeat enhance adaptive immunity to influenza A virus.</ArticleTitle><Pagination><MedlinePgn>46-52</MedlinePgn></Pagination><ELocationID EIdType="doi" ValidYN="Y">10.1016/j.bbi.2010.07.243</ELocationID><Abstract><AbstractText>Dendritic cells (DCs) sample their surrounding microenvironment and consequently send immunogenic or regulatory signals to T cells during DC/T cell interactions, shaping the primary adaptive immune response to infection. The microenvironment resulting from repeated social defeat increases DC co-stimulatory molecule expression and primes DCs for enhanced cytokine responses in vitro. In this study, we show that social disruption stress (SDR) results in the generation of immunogenic DCs, capable of conferring enhanced adaptive immunity to influenza A/PR/8/34 infection. Mice infected with influenza A/PR/8/34 virus 24 h after the adoptive transfer of DCs from SDR mice had significantly increased numbers of D(b)NP(366-74)CD8(+) T cells, increased IFN-γ and IFN-α mRNA, and decreased influenza M1 mRNA expression in the lung during the peak primary response (9 days post-infection), compared to mice that received DCs from naïve mice. These data demonstrate that repeated social defeat is a significant environmental influence on immunogenic DC activation and function.</AbstractText><CopyrightInformation>Copyright © 2010 Elsevier Inc. All rights reserved.</CopyrightInformation></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Powell</LastName><ForeName>Nicole D</ForeName><Initials>ND</Initials><AffiliationInfo><Affiliation>Section of Oral Biology, College of Dentistry, The Ohio State University, Columbus, OH, USA. Nicole.Powell@osumc.edu</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Mays</LastName><ForeName>Jacqueline W</ForeName><Initials>JW</Initials></Author><Author ValidYN="Y"><LastName>Bailey</LastName><ForeName>Michael T</ForeName><Initials>MT</Initials></Author><Author ValidYN="Y"><LastName>Hanke</LastName><ForeName>Mark L</ForeName><Initials>ML</Initials></Author><Author ValidYN="Y"><LastName>Sheridan</LastName><ForeName>John F</ForeName><Initials>JF</Initials></Author></AuthorList><Language>eng</Language><GrantList CompleteYN="Y"><Grant><GrantID>R01 MH046801-16</GrantID><Acronym>MH</Acronym><Agency>NIMH NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>T32DE014320-6</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01MH046801-16</GrantID><Acronym>MH</Acronym><Agency>NIMH NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>R01 MH046801</GrantID><Acronym>MH</Acronym><Agency>NIMH NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>T32 DE014320-06</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant><Grant><GrantID>T32 DE014320</GrantID><Acronym>DE</Acronym><Agency>NIDCR NIH HHS</Agency><Country>United States</Country></Grant></GrantList><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D052061">Research Support, N.I.H., Extramural</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2010</Year><Month>07</Month><Day>23</Day></ArticleDate></Article><MedlineJournalInfo><Country>Netherlands</Country><MedlineTA>Brain Behav Immun</MedlineTA><NlmUniqueID>8800478</NlmUniqueID><ISSNLinking>0889-1591</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D000956">Antigens, 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MajorTopicYN="N">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018845" MajorTopicYN="N">CD11 Antigens</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D018414" MajorTopicYN="N">CD8-Positive T-Lymphocytes</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="N">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D002452" MajorTopicYN="N">Cell Count</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D003163" MajorTopicYN="N">Competitive Behavior</DescriptorName><QualifierName UI="Q000502" MajorTopicYN="Y">physiology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D003713" MajorTopicYN="N">Dendritic Cells</DescriptorName><QualifierName UI="Q000276" MajorTopicYN="Y">immunology</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D000939" MajorTopicYN="N">Epitopes</DescriptorName><QualifierName UI="Q000276" 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