Source:http://linkedlifedata.com/resource/pubmed/id/11934729
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
|
pubmed:dateCreated |
2002-4-5
|
pubmed:abstractText |
The objective of this study was to test the hypothesis that accumulated helper T lymphocytes in malignant pleural effusions may shift to T-helper type 2 (Th2) and produce soluble ST2 protein. We took samples of serum and pleural effusions (p-) from patients with carcinomatous pleurisy (CA, n = 17), tuberculous pleurisy (TB, n = 8), and congestive heart failure (HF, n = 5) and compared the concentration of cytokines or ST2. Ex vivo production of interleukin (IL)-4 and IL-10, though not that of interferon (IFN)-gamma or IL-12, from CD4+ T cells isolated from pleural effusions was higher in the CA group than in the TB or HF group. The p-ST2 concentrations were significantly higher in the CA group than in the TB or HF group, positively correlated with the percentage of pleural effusion CD4+ T cells (r = 0.432, p = 0.016) and inversely correlated with p-IFN-gamma concentrations (r = -0.423, p = 0.019). Furthermore, mRNA expression of ST2 in CD4+ T cells isolated from group CA was upregulated, compared with that in those isolated from the TB group. These results suggest that CD4+ T cells in CA shift to Th2, which can produce soluble ST2 protein, resulting in increased concentrations of p-ST2 in malignant pleural effusion.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cytokines,
http://linkedlifedata.com/resource/pubmed/chemical/IL1RL1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cell Surface
|
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
1073-449X
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
165
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1005-9
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:11934729-CD4-Positive T-Lymphocytes,
pubmed-meshheading:11934729-Cytokines,
pubmed-meshheading:11934729-Heart Failure,
pubmed-meshheading:11934729-Humans,
pubmed-meshheading:11934729-Lung Neoplasms,
pubmed-meshheading:11934729-Lymphocyte Subsets,
pubmed-meshheading:11934729-Membrane Proteins,
pubmed-meshheading:11934729-Pleural Effusion, Malignant,
pubmed-meshheading:11934729-Proteins,
pubmed-meshheading:11934729-RNA, Messenger,
pubmed-meshheading:11934729-Receptors, Cell Surface,
pubmed-meshheading:11934729-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:11934729-T-Lymphocytes, Helper-Inducer,
pubmed-meshheading:11934729-Tuberculosis, Pleural
|
pubmed:year |
2002
|
pubmed:articleTitle |
Expression of ST2 in helper T lymphocytes of malignant pleural effusions.
|
pubmed:affiliation |
Division of Pulmonary Medicine, Department of Medicine, Jichi Medical School, Minamikawachi, Tochigi, Japan. oshikatu@jichi.ac.jp
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|