Steroid-resistant asthma: effects of glucocorticoids on interleukin-4 and interleukin-5 gene expression
- Author:
Yongchang SUN
1
;
Weici LUO
;
Rubing ZHAO
;
Tianxiang GAO
Author Information
1. Peking Union Medical College Hospital
- From:
Chinese Medical Journal
1998;111(9):775-778
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the role of interleukin-4 (IL-4) and interleukin-5 (IL-5) in the pathogenesis of steroid-resistant (SR) asthma.Methods Fifteen patients with SR asthma and 15 patients with steroid-sensitive (SS) asthma were selected based on their clinical responses to prednisone therapy. The peripheral blood mononuclear cells (PBMCs) were obtained and incubated with phytohemagglutinin (PHA) in vitro for 48 h in the presence or absence of dexamethasone (10-7 mol/L). Expressions of IL-4 and IL-5 mRNA in PBMCs were determined by reverse transcription-polymerase chain reaction (RT-PCR), and mRNA positive PBMCs for IL-4 and IL-5 were measured with in situ hybridization using digoxin-labeled cDNA probes.Results In the absence of dexamethasone, there was no significant difference in the expressions of IL-4 and IL-5 mRNA between SR and SS asthmatics, and the numbers of mRNA positive cells for IL-4 and IL-5 were also similar between these two groups, however, in the presence of dexamethasone (10-7 mol/L), expressions of IL-4 mRNA (P<0.01) and IL-5 mRNA (P<0.05) were significantly inhibited in SS asthmatics, but not in SR asthmatics (P>0.05). The numbers of IL-4 and IL-5 mRNA positive cells decreased from 5.50±1.60 to 2.27±0.98 (P<0.01) and from 5.03±1.29 to 1.67±0.70 (P<0.01), respectively in SS asthmatics, but in the patients with SR asthma, there was no significant change in the number of cells expressing mRNA for IL-4 or IL-5.Conclusion The gene expression of IL-4 and IL-5 in SR asthma was not inhibited by dexamethasone at the concentration of 10-7 mol/L. It is suggested that the relative unresponsiveness of T cells to glucocorticoids and persistent production of cytokines may be one of the mechanisms of steroid resistance in asthma.
