Source:http://linkedlifedata.com/resource/pubmed/id/15914842
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
Pt 6
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pubmed:dateCreated |
2005-5-25
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pubmed:abstractText |
Herpes simplex virus type 1 (HSV-1) is able to establish latency in infected individuals. In order to characterize potential new immune-escape mechanisms, mature dendritic cells (DCs) were infected with HSV-1 and total cellular RNA was isolated from infected and mock-infected populations at different time points. RNA profiling on Affymetrix Human Genome U133A arrays demonstrated a dramatic downregulation of the migration-mediating surface molecules CCR7 and CXCR4, an observation that was further confirmed by RT-PCR and fluorescence-activated cell sorting analyses. Furthermore, migration assays revealed that, upon infection of mature DCs, CCR7- and CXCR4-mediated migration towards the corresponding CCL19 and CXCL12 chemokine gradients was strongly reduced. It is noteworthy that the infection of immature DCs with HSV-1 prior to maturation led to a failure of CCR7 and CXCR4 upregulation during DC maturation and, as a consequence, also induced a block in their migratory capacity. Additional migration assays with a Deltavhs mutant virus lacking the virion host shutoff (vhs) gene, which is known to degrade cellular mRNAs, suggested a vhs-independent mechanism. These results indicate that HSV-1-infected mature DCs are limited in their capacity to migrate to secondary lymphoid organs, the areas of antigen presentation and T-cell stimulation, thus inhibiting an antiviral immune response. This represents a novel, previously unrecognized mechanism for HSV-1 to escape the human immune system.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CCR7 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR7,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CXCR4,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Chemokine,
http://linkedlifedata.com/resource/pubmed/chemical/Ribonucleases,
http://linkedlifedata.com/resource/pubmed/chemical/Viral Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/virion host shutoff protein...
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0022-1317
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pubmed:author |
pubmed-author:CoffinRobert SRS,
pubmed-author:EisemannJutta IJI,
pubmed-author:HackerChristineC,
pubmed-author:JuXinshengX,
pubmed-author:KobeltDieter JDJ,
pubmed-author:McGrathYvonneY,
pubmed-author:PrechtelAlexander TAT,
pubmed-author:SteinkassererAlexanderA,
pubmed-author:TurzaNadine MNM,
pubmed-author:ZenkeMartinM
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pubmed:issnType |
Print
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pubmed:volume |
86
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1645-57
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:15914842-Cell Differentiation,
pubmed-meshheading:15914842-Cell Movement,
pubmed-meshheading:15914842-Dendritic Cells,
pubmed-meshheading:15914842-Down-Regulation,
pubmed-meshheading:15914842-Herpes Simplex,
pubmed-meshheading:15914842-Herpesvirus 1, Human,
pubmed-meshheading:15914842-Humans,
pubmed-meshheading:15914842-Mutation,
pubmed-meshheading:15914842-RNA, Messenger,
pubmed-meshheading:15914842-Receptors, CCR7,
pubmed-meshheading:15914842-Receptors, CXCR4,
pubmed-meshheading:15914842-Receptors, Chemokine,
pubmed-meshheading:15914842-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:15914842-Ribonucleases,
pubmed-meshheading:15914842-Time Factors,
pubmed-meshheading:15914842-Viral Proteins
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pubmed:year |
2005
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pubmed:articleTitle |
Infection of mature dendritic cells with herpes simplex virus type 1 dramatically reduces lymphoid chemokine-mediated migration.
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pubmed:affiliation |
Department of Dermatology, University Hospital Erlangen, Hartmannstrasse 14, D-91052 Erlangen, Germany. derma.imed.uni-erlangen.de
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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