Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1992-5-14
pubmed:abstractText
We have studied the phenotype and activation status of leukocytes in the bronchial mucosa in patients with isocyanate-induced asthma. Fiberoptic bronchial biopsy specimens were obtained from nine subjects with occupational (five toluene- and four methylene diisocyanate-sensitive) asthma, 10 subjects with extrinsic asthma, and 12 nonatopic healthy control subjects. Bronchial biopsy specimens were examined by immunohistology with a panel of monoclonal antibodies and the alkaline phosphatase-antialkaline phosphatase method. There was a significant increase in the number of CD25+ cells (interleukin-2 receptor-bearing cells, presumed "activated" T-lymphocytes; p less than 0.01) in isocyanate-induced asthma compared with that of control subjects. There were also significant increases in major basic protein (BMK-13)-positive (p less than 0.02) and EG2-positive (p less than 0.01) cells that represent total and "activated" eosinophil cationic protein-secreting eosinophils, respectively. In agreement with our previous findings, CD25+ (p less than 0.01), BMK-13 (p less than 0.03), and EG2+ (p less than 0.01) cells were also elevated in extrinsic asthma. No significant differences were observed in the numbers of T-lymphocyte phenotypic markers (CD3, CD4, and CD8) between subjects with asthma (isocyanate-induced and extrinsic) and control subjects. Similarly, no significant differences in immunostaining for neutrophil elastase (neutrophils) or CD68 (macrophages) were observed. The results suggest that isocyanate-induced occupational asthma and atopic (extrinsic) asthma have a similar pattern of inflammatory cell infiltrate. The results support the view that T-lymphocyte activation and eosinophil recruitment may be important in asthma of diverse etiology.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0091-6749
pubmed:author
pubmed:issnType
Print
pubmed:volume
89
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
821-9
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:1532807-Adult, pubmed-meshheading:1532807-Antigens, CD, pubmed-meshheading:1532807-Antigens, CD45, pubmed-meshheading:1532807-Asthma, pubmed-meshheading:1532807-Biopsy, pubmed-meshheading:1532807-Bronchi, pubmed-meshheading:1532807-Cyanates, pubmed-meshheading:1532807-Drug Hypersensitivity, pubmed-meshheading:1532807-Eosinophils, pubmed-meshheading:1532807-Female, pubmed-meshheading:1532807-Histocompatibility Antigens, pubmed-meshheading:1532807-Humans, pubmed-meshheading:1532807-Immunohistochemistry, pubmed-meshheading:1532807-Lymphocyte Activation, pubmed-meshheading:1532807-Male, pubmed-meshheading:1532807-Middle Aged, pubmed-meshheading:1532807-Mucous Membrane, pubmed-meshheading:1532807-Occupational Diseases, pubmed-meshheading:1532807-Receptors, Interleukin-2, pubmed-meshheading:1532807-T-Lymphocytes
pubmed:year
1992
pubmed:articleTitle
Activated T-lymphocytes and eosinophils in the bronchial mucosa in isocyanate-induced asthma.
pubmed:affiliation
Department of Allergy and Clinical Immunology, National Heart & Lung Institute, London, England.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't