Markers of allergic inflammation in peripheral blood of children with asthma after treatment with inhaled triamcinolone acetonide

Citation
I. Stelmach et al., Markers of allergic inflammation in peripheral blood of children with asthma after treatment with inhaled triamcinolone acetonide, ANN ALLER A, 87(4), 2001, pp. 319-326
Citations number
39
Categorie Soggetti
Clinical Immunolgy & Infectious Disease
Journal title
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY
ISSN journal
10811206 → ACNP
Volume
87
Issue
4
Year of publication
2001
Pages
319 - 326
Database
ISI
SICI code
1081-1206(200110)87:4<319:MOAIIP>2.0.ZU;2-V
Abstract
Background: It is important to monitor inflammation regularly in asthma in addition to clinical symptoms, and there is a great need for noninvasive te sts that could routinely be used in clinical practice. Objective: Our hypothesis was that the improvement of clinical parameters, together with decreased airway responsiveness, could be correlated with cha nges in the levels of serum markers of inflammation after a 4-week treatmen t with triamcinolone. Methods: In this double-blind, randomized, placebo-controlled trial, 48 chi ldren, aged 6 to 18 years, with mild to moderate atopic asthma, were random ly allocated to receive triamcinolone or matching placebo for 4 weeks. The following parameters were measured: the symptom score, forced expiratory vo lume in I second (FEV1), provocative concentration of histamine causing a 2 0% fall in FEV1 (PC20) for histamine and peripheral blood eosinophil count, serum levels of the inflammatory markers eosinophil cationic protein (ECP) , soluble receptor of interleukin-2 (sIL-2R), interleukin-4, soluble interc ellular adhesion molecule-1 before and after treatment. Results: The clinical parameters significantly improved after treatment wit h triamcinolone, the mean value of FEV1 changed from 74% of predicted value before, to 90% of predicted after treatment (P < 0.0001). PC20 for histami ne after treatment with triamcinolone increased significantly from the mean value 2.5 mg/mL to 4.7 mg/mL (P < 0.001). Treatment with triamcinolone sig nificantly (P < 0.05) decreased serum levels of all the measured inflammato ry markers. The mean concentration of eosinophil blood count was 380 and 26 1 cells/mm(3); ECP, 83 and 58 ng/mL; serum sIL-2R, 734 and 487 pg/mL; solub le intercellular adhesion molecule-1, 266 and 210 ng/mL, before and after t reatment, respectively. The values of interleukin-4 were low and close to t he sensitivity of the assay. A significant correlation was found between EC P and sIL-2R levels before and after treatment with triamcinolone. Conclusions: A significant decrease of all the measured serum parameters wa s observed after treatment with triamcinolone; however, no significant corr elation was found among any of those parameters and clinical markers of dis ease severity (such as FEV1 or PC20H).