Source:http://linkedlifedata.com/resource/pubmed/id/21525347
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
13
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pubmed:dateCreated |
2011-6-10
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pubmed:abstractText |
Interleukin-10 (IL-10) mRNA is rapidly upregulated in the central nervous system (CNS) following infection with neurotropic coronavirus and remains elevated during persistent infection. Infection of transgenic IL-10/green fluorescent protein (GFP) reporter mice revealed that CNS-infiltrating T cells were the major source of IL-10, with minimal IL-10 production by macrophages and resident microglia. The proportions of IL-10-producing cells were initially similar in CD8(+) and CD4(+) T cells but diminished rapidly in CD8(+) T cells as the virus was controlled. Overall, the majority of IL-10-producing CD8(+) T cells were specific for the immunodominant major histocompatibility complex (MHC) class I epitope. Unlike CD8(+) T cells, a large proportion of CD4(+) T cells within the CNS retained IL-10 production throughout persistence. Furthermore, elevated frequencies of IL-10-producing CD4(+) T cells in the spinal cord supported preferential maintenance of IL-10 production at the site of viral persistence and tissue damage. IL-10 was produced primarily by the CD25(+) CD4(+) T cell subset during acute infection but prevailed in CD25(-) CD4(+) T cells during the transition to persistent infection and thereafter. Overall, these data demonstrate significant fluidity in the T-cell-mediated IL-10 response during viral encephalitis and persistence. While IL-10 production by CD8(+) T cells was limited primarily to the time of acute effector function, CD4(+) T cells continued to produce IL-10 throughout infection. Moreover, a shift from predominant IL-10 production by CD25(+) CD4(+) T cells to CD25(-) CD4(+) T cells suggests that a transition to nonclassical regulatory T cells precedes and is retained during CNS viral persistence.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1098-5514
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
85
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6702-13
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pubmed:meshHeading |
pubmed-meshheading:21525347-Acute Disease,
pubmed-meshheading:21525347-Animals,
pubmed-meshheading:21525347-CD4-Positive T-Lymphocytes,
pubmed-meshheading:21525347-CD8-Positive T-Lymphocytes,
pubmed-meshheading:21525347-Central Nervous System,
pubmed-meshheading:21525347-Chronic Disease,
pubmed-meshheading:21525347-Encephalitis, Viral,
pubmed-meshheading:21525347-Encephalomyelitis,
pubmed-meshheading:21525347-Interleukin-10,
pubmed-meshheading:21525347-Interleukin-2 Receptor alpha Subunit,
pubmed-meshheading:21525347-Mice,
pubmed-meshheading:21525347-Mice, Inbred C57BL,
pubmed-meshheading:21525347-Murine hepatitis virus,
pubmed-meshheading:21525347-T-Lymphocyte Subsets
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pubmed:year |
2011
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pubmed:articleTitle |
Shifting hierarchies of interleukin-10-producing T cell populations in the central nervous system during acute and persistent viral encephalomyelitis.
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pubmed:affiliation |
Department of Neuroscience, Lerner Research Institute, The Cleveland Clinic, 9500 Euclid Avenue, NC30, Cleveland, OH 44195, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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