Source:http://linkedlifedata.com/resource/pubmed/id/15882355
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2005-5-10
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pubmed:abstractText |
A decline in T-cell responses and a switch to memory T-cell predominance occur with aging. We have used the T-cell receptor (TCR) transgenic mouse model to study age-associated changes in T-cell responses that are a consequence of shifts in subset representation versus changes intrinsic to T cells versus changes in the 'aged' microenvironment. We found that naive transgene-expressing (Tg(+)) CD4(+) T cells from aged mice respond to antigen with reduced interleukin-2 (IL-2) production, decreased cell expansion, and limited differentiation to effectors. Comparable to the characteristic accumulation of memory phenotype T cells in aged humans and conventional rodents, Tg(+) CD4(+) T cells from old OTII and 6.5 TCR transgenic mice acquire a memory phenotype without immunization and become hyporesponsive. The naive Tg(+) CD8(+) T cells from aged 2C mice expressed activation markers, produced IL-2, proliferated, and differentiated into cytotoxic T lymphocytes as efficiently as their young counterparts. Responses by adoptive transferred Tg(+) cells from young mice, immunized in young and old conventional hosts, indicated that the host age influences the onset of cell division, level of cell expansion, and number of cytokine-producing cells. Co-transfer of dendritic cells (DCs) from young and less so from aged conventional mice partially restored responses. Furthermore, DCs and T-cell migration to draining lymphoid organs was reduced due to deficiencies intrinsic to aged cells and the aged environment. Thus, alterations in T-cell responses in aging are attributable to intrinsic and environmental influences.
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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 |
Jun
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pubmed:issn |
0105-2896
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
205
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
207-19
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:15882355-Aging,
pubmed-meshheading:15882355-Animals,
pubmed-meshheading:15882355-Antigens,
pubmed-meshheading:15882355-Cell Proliferation,
pubmed-meshheading:15882355-Environment,
pubmed-meshheading:15882355-Humans,
pubmed-meshheading:15882355-Receptors, Antigen, T-Cell,
pubmed-meshheading:15882355-T-Lymphocytes
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pubmed:year |
2005
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pubmed:articleTitle |
Intrinsic versus environmental influences on T-cell responses in aging.
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pubmed:affiliation |
Sidney Kimmel Cancer Center, San Diego, CA 92121, USA. plinton@skcc.org
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Review,
Research Support, N.I.H., Extramural
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