Transcriptional phenotypes of asthma defined by gene expression profiling of induced sputum samples

J Allergy Clin Immunol. 2011 Jan;127(1):153-60, 160.e1-9. doi: 10.1016/j.jaci.2010.10.024.

Abstract

Background: Previous studies have identified clinical or inflammatory phenotypes of asthma on the basis of clinical and demographic parameters or sputum cell counts; however, few studies have defined transcriptional phenotypes of asthma.

Objective: To investigate asthma phenotypes at a transcriptional level by using gene expression profiling of induced sputum.

Methods: Induced sputum samples were collected from 59 people with asthma with a mean age of 58 years and an FEV(1)% predicted of 76%, and 69% were taking inhaled corticosteroids. Thirteen healthy controls without asthma were also assessed. Inflammatory cell counts were performed, and RNA was extracted from selected sputum. Transcriptional profiles were generated (Illumina Humanref-8 V2) and analyzed by using GeneSpring GX11.

Results: Unsupervised hierarchical clustering of gene expression profiles in asthma revealed 3 distinct groups. The first transcriptional phenotype (n = 21) had lower FEV(1)% predicted and higher asthma control questionnaire scores, exhaled nitric oxide, and sputum eosinophils. The second transcriptional phenotype (n = 14) had lower FEV(1)% predicted and forced vital capacity % predicted and higher sputum neutrophils compared with a third transcriptional phenotype (n = 24) that had higher sputum macrophages and resembled healthy controls. Differentially expressed genes between transcriptional asthma phenotypes were related to inflammatory and immune responses. Genes in the IL-1 and TNF-α/nuclear factor-κB pathways were overexpressed and correlated with clinical parameters and neutrophilic airway inflammation.

Conclusion: Gene expression profiling provides a novel means to investigate the molecular mechanisms and classifications of asthma phenotypes. There are 3 distinct transcriptional phenotypes of asthma that relate to both clinical and inflammatory parameters.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Asthma / genetics*
  • Asthma / immunology*
  • Asthma / metabolism
  • Cluster Analysis
  • Female
  • Gene Expression Profiling*
  • Humans
  • Interleukin-1 / biosynthesis
  • Interleukin-1 / immunology
  • Male
  • Middle Aged
  • NF-kappa B / biosynthesis
  • NF-kappa B / immunology
  • Oligonucleotide Array Sequence Analysis
  • Phenotype
  • Respiratory Function Tests
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sputum / chemistry
  • Sputum / immunology*
  • Sputum / metabolism
  • Transcription, Genetic
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Interleukin-1
  • NF-kappa B
  • Tumor Necrosis Factor-alpha