Source:http://linkedlifedata.com/resource/pubmed/id/16818741
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2006-7-4
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pubmed:abstractText |
Mechanisms for the generation of memory CD4 T cells and their delineation into diverse subsets remain largely unknown. In this study, we demonstrate in two Ag systems, divergent generation of heterogeneous memory CD4 T cells from activated precursors in distinct differentiation stages. Specifically, we show that influenza hemagglutinin- and OVA-specific CD4 T cells activated for 1, 2, and 3 days, respectively, exhibit gradations of differentiation by cell surface phenotype, IFN-gamma production, and proliferation, yet all serve as direct precursors for functional memory CD4 T cells when transferred in vivo into Ag-free mouse hosts. Using a conversion assay to track the immediate fate of activated precursors in vivo, we show that day 1- to 3-activated cells all rapidly convert from an activated phenotype (CD25(high)IL-7R(low)CD44(high)) to a resting memory phenotype (IL-7R(high)CD25(low)CD44(high)) 1 day after antigenic withdrawal. Paradoxically, stable memory subset delineation from undifferentiated (day 1- to 2-activated) precursors was predominantly an effector memory (CD62L(low)) profile, with an increased proportion of central memory (CD62L(high)) T cells arising from more differentiated (day 3-activated) precursors. Our findings support a divergent model for generation of memory CD4 T cells directly from activated precursors in multiple differentiation states, with subset heterogeneity maximized by increased activation and differentiation during priming.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
177
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
869-76
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16818741-Amino Acid Sequence,
pubmed-meshheading:16818741-Animals,
pubmed-meshheading:16818741-CD4-Positive T-Lymphocytes,
pubmed-meshheading:16818741-Cell Differentiation,
pubmed-meshheading:16818741-Cells, Cultured,
pubmed-meshheading:16818741-Epitopes, T-Lymphocyte,
pubmed-meshheading:16818741-Hemagglutinin Glycoproteins, Influenza Virus,
pubmed-meshheading:16818741-Immunologic Memory,
pubmed-meshheading:16818741-Lymphocyte Activation,
pubmed-meshheading:16818741-Mice,
pubmed-meshheading:16818741-Mice, Inbred BALB C,
pubmed-meshheading:16818741-Mice, Transgenic,
pubmed-meshheading:16818741-Molecular Sequence Data,
pubmed-meshheading:16818741-Ovalbumin,
pubmed-meshheading:16818741-Stem Cells,
pubmed-meshheading:16818741-Time Factors
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pubmed:year |
2006
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pubmed:articleTitle |
Divergent generation of heterogeneous memory CD4 T cells.
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pubmed:affiliation |
Department of Surgery, Division of Transplantation, University of Maryland School of Medicine, 685 West Baltimore Street, Baltimore, MD 21201, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, N.I.H., Extramural
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