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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0001511,
umls-concept:C0014257,
umls-concept:C0014467,
umls-concept:C0017262,
umls-concept:C0021368,
umls-concept:C0063695,
umls-concept:C0086597,
umls-concept:C0115305,
umls-concept:C0221912,
umls-concept:C0225336,
umls-concept:C0700624,
umls-concept:C1171362,
umls-concept:C1515655,
umls-concept:C1515670,
umls-concept:C1533691
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pubmed:issue |
2
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pubmed:dateCreated |
1991-2-19
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pubmed:abstractText |
We have compared the adhesion of 51Cr-labeled eosinophils and neutrophils to cultured human umbilical vein endothelial cell (EC) monolayers that have been stimulated with IL-1, TNF, or LPS. Each agent stimulated the adhesion to EC of both eosinophils and neutrophils in a similar dose- and time-dependent manner. F(ab')2 fragments of mAb 1.2B6 (anti-endothelial leukocyte adhesion molecule (ELAM)-1) and mAb 6.5B5 (anti-intercellular adhesion molecule (ICAM)-1) each inhibited partially, and to a similar extent, eosinophil and neutrophil adhesion to EC monolayers prestimulated with TNF (10 ng/ml) for 6 h. Greater inhibition of both eosinophil and neutrophil adhesion was achieved by combining the effects of mAb 1.2B6 with either mAb 6.5B5 or mAb TS1/18 (anti-CD18). These observations indicate that both ELAM-1 and ICAM-1 are involved in the adhesion of eosinophils and neutrophils to EC stimulated with TNF. In order to determine whether these molecules are expressed in vivo during allergen-induced late phase allergic responses in the skin, human skin biopsies were examined at 6 h after Ag or saline challenge with the use of an alkaline phosphatase-staining technique. Both ELAM-1 and ICAM-1 were expressed with greater intensities in Ag-challenged biopsies, suggesting that these molecules may be involved in granulocyte recruitment in vivo. The similarities we have established between mechanisms of eosinophil and neutrophil adhesion to cytokine-stimulated EC suggests that factors other than differential leukocyte-EC adhesion may be responsible for the selective accumulation of eosinophils at sites of allergic inflammation.
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pubmed:grant | |
pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules,
http://linkedlifedata.com/resource/pubmed/chemical/E-Selectin,
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Adhesion Molecule-1,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2,
http://linkedlifedata.com/resource/pubmed/chemical/Lipopolysaccharides,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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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 |
146
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
521-8
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pubmed:dateRevised |
2010-8-25
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pubmed:meshHeading |
pubmed-meshheading:1702804-Adult,
pubmed-meshheading:1702804-Antibodies, Monoclonal,
pubmed-meshheading:1702804-Cell Adhesion,
pubmed-meshheading:1702804-Cell Adhesion Molecules,
pubmed-meshheading:1702804-Dermatitis,
pubmed-meshheading:1702804-E-Selectin,
pubmed-meshheading:1702804-Endothelium, Vascular,
pubmed-meshheading:1702804-Eosinophils,
pubmed-meshheading:1702804-Humans,
pubmed-meshheading:1702804-Hypersensitivity,
pubmed-meshheading:1702804-Intercellular Adhesion Molecule-1,
pubmed-meshheading:1702804-Interleukin-2,
pubmed-meshheading:1702804-Lipopolysaccharides,
pubmed-meshheading:1702804-Middle Aged,
pubmed-meshheading:1702804-Neutrophils,
pubmed-meshheading:1702804-Receptors, Immunologic,
pubmed-meshheading:1702804-Skin,
pubmed-meshheading:1702804-Tumor Necrosis Factor-alpha
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pubmed:year |
1991
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pubmed:articleTitle |
Endothelial leukocyte adhesion molecule-1 and intercellular adhesion molecule-1 mediate the adhesion of eosinophils to endothelial cells in vitro and are expressed by endothelium in allergic cutaneous inflammation in vivo.
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pubmed:affiliation |
Department of Allergy, United Medical School, Guy's Hospital, London, U.K.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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