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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1991-4-22
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pubmed:abstractText |
Lymphokines derived from activated T cells regulate the proliferation and postmitotic differentiation of eosinophils in vitro. We investigated whether peripheral blood eosinophilia, which is a characteristic feature of both allergic and nonallergic asthma, correlates with T cell activation and lymphokine production in asthmatic patients. Flow cytometric analysis of T cell activation markers revealed that asthmatic individuals are characterized by increased numbers of IL-2R (CD25)-bearing T cell subsets. The absolute number of IL-2R+ T cells correlated with the eosinophilia observed in the asthmatic patients. Purified CD4+ and CD8+ T cells from allergic and nonallergic asthmatic individuals spontaneously secreted factors that extend the lifespan of eosinophils in vitro. T cells from normal donors displayed this effect only after polyclonal stimulation with anti-CD3 antibody. The eosinophil lifespan-extending factors were also found in sera of asthmatic patients. Identification of these factors was performed by using neutralizing antibodies against IL-3, IL-5, and granulocyte-macrophage CSF. In sera, mainly IL-5 and granulocyte-macrophage CSF were responsible for prolonged eosinophil survival, whereas granulocyte-macrophage CSF was dominant in T cell supernatants. These results indicate that T cells and secretion of lymphokines play an important regulatory function toward eosinophils, which are thought to represent major proinflammatory effector cells in certain types of asthma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD8,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Differentiation...,
http://linkedlifedata.com/resource/pubmed/chemical/Culture Media,
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Interleukin-2
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
146
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1829-35
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1672334-Adult,
pubmed-meshheading:1672334-Aged,
pubmed-meshheading:1672334-Antigens, CD,
pubmed-meshheading:1672334-Antigens, CD8,
pubmed-meshheading:1672334-Antigens, Differentiation, T-Lymphocyte,
pubmed-meshheading:1672334-Asthma,
pubmed-meshheading:1672334-CD4-Positive T-Lymphocytes,
pubmed-meshheading:1672334-Culture Media,
pubmed-meshheading:1672334-Cytokines,
pubmed-meshheading:1672334-Eosinophilia,
pubmed-meshheading:1672334-Female,
pubmed-meshheading:1672334-Humans,
pubmed-meshheading:1672334-Lymphocyte Activation,
pubmed-meshheading:1672334-Male,
pubmed-meshheading:1672334-Middle Aged,
pubmed-meshheading:1672334-Receptors, Interleukin-2,
pubmed-meshheading:1672334-T-Lymphocyte Subsets
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pubmed:year |
1991
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pubmed:articleTitle |
T cell subsets and their soluble products regulate eosinophilia in allergic and nonallergic asthma.
|
pubmed:affiliation |
Swiss Institute of Allergy and Asthma Research, Davos.
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro
|