Source:http://linkedlifedata.com/resource/pubmed/id/14991598
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2004-3-1
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pubmed:abstractText |
Naive CD4 T cells develop Th2 activity early in primary responses to alum-precipitated proteins by producing IL-4 mRNA and inducing B cells to produce gamma1 and epsilon switch transcripts. Both IL-4-dependent and IL-4-independent pathways for IL-4 induction are recognized, but their relative contribution to the different phases of primary Th2 responses in vivo is uncertain. We show the primary induction of IL-4 synthesis in lymph nodes responding to alum-precipitated protein is overwhelmingly in antigen-specific CD4 T cells and is unimpaired in IL-4Ralpha(-/-) mice, which can produce but do not respond to IL-4 and IL-13. Ig class-switching in extra-follicular responses, reflecting Th2 activity, is also unimpaired in these mice. By contrast, 7 days after immunization--when T cells are selecting B cells in germinal centers and T cell priming has occurred--non-responsiveness to IL-4 is associated with smaller germinal centers, increased levels of T-bet and gamma2a switch transcripts and reduced gamma1 and epsilon transcripts. These data indicate that Th2 characteristics acquired during T cell priming and the initial CD4 T cell interaction with B cells are largely IL-4-independent, whereas IL-4 production induced during priming has a significant role in maintaining the Th2 phenotype as T cells select B cells in germinal centers.
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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 |
Mar
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pubmed:issn |
0014-2980
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
34
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
686-94
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14991598-Animals,
pubmed-meshheading:14991598-Antibody Formation,
pubmed-meshheading:14991598-B-Lymphocytes,
pubmed-meshheading:14991598-CD4-Positive T-Lymphocytes,
pubmed-meshheading:14991598-Cells, Cultured,
pubmed-meshheading:14991598-Germinal Center,
pubmed-meshheading:14991598-Interleukin-13,
pubmed-meshheading:14991598-Interleukin-4,
pubmed-meshheading:14991598-Lymph Nodes,
pubmed-meshheading:14991598-Lymphocyte Activation,
pubmed-meshheading:14991598-Mice,
pubmed-meshheading:14991598-Mice, Knockout,
pubmed-meshheading:14991598-Ovalbumin,
pubmed-meshheading:14991598-Receptors, Interleukin-4,
pubmed-meshheading:14991598-Signal Transduction,
pubmed-meshheading:14991598-Th1 Cells,
pubmed-meshheading:14991598-Th2 Cells
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pubmed:year |
2004
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pubmed:articleTitle |
Pinpointing IL-4-independent acquisition and IL-4-influenced maintenance of Th2 activity by CD4 T cells.
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pubmed:affiliation |
The Medical Research Council Centre for Immune Regulation, University of Birmingham, Birmingham, GB.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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