Source:http://linkedlifedata.com/resource/pubmed/id/15277404
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rdf:type | |
lifeskim:mentions |
umls-concept:C0003209,
umls-concept:C0011306,
umls-concept:C0033414,
umls-concept:C0079189,
umls-concept:C0086418,
umls-concept:C0108747,
umls-concept:C0234402,
umls-concept:C0445356,
umls-concept:C0851285,
umls-concept:C0871261,
umls-concept:C1414555,
umls-concept:C1515895,
umls-concept:C1515999,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2348205,
umls-concept:C2911692
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pubmed:issue |
9
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pubmed:dateCreated |
2004-8-16
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pubmed:abstractText |
We previously demonstrated that tumor necrosis factor (TNF)-alpha-matured CD16- and CD16+ human monocyte-derived dendritic cells (16-mDC and 16+mDC) differentially stimulate naive CD4+ lymphocytes by inducing Th1- and Th2-like responses, respectively. Here, we further characterized the role of different DC maturation factors on Th polarization. Immature 16+mDC and 16-mDC (iDC) obtained by culture of purified monocytes with GM-CSF and IL-4 were maturated with (i) Toll-like receptor (TLR) ligands [lipopolysaccharide (LPS)], (ii) lymphocyte-derived (soluble CD40 ligand, IFN-gamma) and (iii) endogenous inflammatory stimuli [TNF-alpha, prostaglandin (PG)E2]. After activation with these stimuli, DC secrete IL-12 only in presence of LPS, and 16+mDC produced lower amounts of IL-12 and IL-10 than 16-mDC. Allogeneic CD4+CD45RO- lymphocytes co-cultured with 16+mDC secreted higher levels of IL-4 and IL-10 than those co-cultured with 16-mDC, regardless of the maturation stimuli. Results were similar when DC were activated with TLR-2 or TLR-3 ligands. The higher induction of IL-4 by 16+mDC was primarily dependent on IL-12, IL-4 and IL-10. IFN-gamma production by CD4+ T cells was similar with all the conditions except with LPS-16+mDC, which induced reduced amounts of this cytokine. Those differences were totally eliminated by neutralization of IL-12, IL-4 or IL-10. Finally, 16-mDC could reverse the Th2 phenotype of already committed lymphocytes toward a Th1 pattern in short-term cultures, whereas 16+mDC had less ability to skew this phenotype. These results indicate that 16+mDC elicit superior Th2 responses independently of the maturation factors that they received, and suggest that they could represent an important population of regulatory DC.
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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/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-10,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-12,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-4,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, IgG
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0953-8178
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1251-63
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:15277404-Cytokines,
pubmed-meshheading:15277404-Dendritic Cells,
pubmed-meshheading:15277404-Humans,
pubmed-meshheading:15277404-Immunophenotyping,
pubmed-meshheading:15277404-Interferon-gamma,
pubmed-meshheading:15277404-Interleukin-10,
pubmed-meshheading:15277404-Interleukin-12,
pubmed-meshheading:15277404-Interleukin-4,
pubmed-meshheading:15277404-Lymphocyte Activation,
pubmed-meshheading:15277404-Monocytes,
pubmed-meshheading:15277404-Receptors, IgG,
pubmed-meshheading:15277404-Th2 Cells
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pubmed:year |
2004
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pubmed:articleTitle |
CD16+ human monocyte-derived dendritic cells matured with different and unrelated stimuli promote similar allogeneic Th2 responses: regulation by pro- and anti-inflammatory cytokines.
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pubmed:affiliation |
Department of Molecular Biomedicine, Centro de Investigación y de Estudios Avanzados-IPN, Instituto de Investigaciones Biomédicas, UNAM, Mexico City, Mexico.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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