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Original article
The usefulness of competitive PCR: airway gene expression of IL-5, IL-4, IL-4δ2, IL-2, and IFNγ in asthma
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  1. E M Glarea,
  2. M Divjaka,
  3. M J Baileyb,
  4. E H Waltersc
  1. aDepartment of Respiratory Medicine, Alfred Hospital and Monash University Medical School, Melbourne, Australia, bDepartment of Epidemiology and Preventive Medicine, cDiscipline of Medicine, University of Tasmania Medical School, Royal Hobart Hospital, Hobart, Australia
  1. Professor E H Waltershaydn.walters{at}utas.edu.au

Abstract

BACKGROUND Asthma has been described as an eosinophilic bronchitis driven by interleukin(IL)-4 and IL-5. The quantification of cytokine mRNA levels in airway samples has been confounded by housekeeping gene expression which differs between and within asthmatics and controls.

METHODS The usefulness of competitive reverse transcriptase-polymerase chain reaction (RT-PCR) that is independent of housekeeping gene expression for quantitating the mRNA for interferon (IFN)γ, IL-2, IL-5, IL-4 and its receptor antagonist encoding splicing variant IL-4δ2 was determined in a cross sectional study of 45 normal control subjects and 111 with asthma.

RESULTS Atopic controls and atopic asthmatic subjects expressed more IL-5 than non-atopic controls (p<0.02) in bronchoalveolar lavage (BAL) cells, but not in biopsy specimens. IL-5 mRNA expression in BAL cells from asthmatic subjects using inhaled corticosteroids (ICS) was significantly lower than those not receiving ICS (p=0.04). IL-2 mRNA levels differed with steroid use in biopsy specimens but not in BAL cells. IFNγ, IL-4, and IL-4δ2 mRNA levels did not differ between any groups and were not affected by steroid use. IL-4 and IL-4δ2 mRNA levels were positively correlated (p<0.0001), suggesting coordinated transcription.

CONCLUSIONS While the signal differentiation of competitive PCR in asthma may rival that of in situ hybridisation and immunohistochemistry, the method is expensive and wasteful of material.

  • asthma
  • competitive PCR
  • interleukins

https://doi.org/10.1136/thx.56.7.541

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