Increased production of IFN-gamma and cysteinyl leukotrienes in virus-induced wheezing

Citation
Sm. Van Schaik et al., Increased production of IFN-gamma and cysteinyl leukotrienes in virus-induced wheezing, J ALLERG CL, 103(4), 1999, pp. 630-636
Citations number
22
Categorie Soggetti
Clinical Immunolgy & Infectious Disease",Immunology
Journal title
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
ISSN journal
00916749 → ACNP
Volume
103
Issue
4
Year of publication
1999
Pages
630 - 636
Database
ISI
SICI code
0091-6749(199904)103:4<630:IPOIAC>2.0.ZU;2-M
Abstract
Background: An imbalance of production of T-helper lymphocyte cytokines, fa voring overproduction of IL-4, is believed to be important in the pathogene sis of allergic asthma. However, less is known about the cytokine response in virus-induced wheezing, which is a major cause of morbidity in asthma. Objective: We undertook this study to determine the magnitude of IFN-gamma, IL-4 and IL-10, and leukotriene (LT) responses in infants and children wit h virus-induced wheezing, Methods: We measured the concentrations of IFN-gamma, IL-4 and IL-10, and c ysteinyl LTs in respiratory secretions of 82 infants and young children dur ing acute episodes of virus-induced wheezing. Control subjects were 47 infa nts and children with uncomplicated upper respiratory infections and 18 nor mal healthy infants. Results: Ratios of IFN-gamma to IL-4 were higher (due to increased quantiti es of IFN-gamma) in subjects with wheezing than in those with upper respira tory infection alone (P =.003). Quantities of LTs were also increased in wh eezing subjects in comparison with those with upper respiratory infections (P =.003), There was a significant correlation between measured concentrati ons of IFN-gamma and LTs (correlation coefficient = .451, P =.007), Quantit ies of IL-4 were slightly suppressed in the wheezing groups. Conclusions: An imbalance favoring overproduction of IFN-gamma appears to b e associated temporarily with virus-induced wheezing. A possible mechanism is the enhanced release of LTs from eosinophils or mast cells after sensiti zation by IFN-gamma.