Abstract

We sought to identify cells and cytokines in bronchoalveolar lavage (BAL) fluids that distinguish asthma from healthy control subjects and those that distinguish controlled asthma from uncontrolled asthma. Following informed consent, 36 human subjects were recruited for this study. These included 11 healthy control subjects, 15 subjects with controlled asthma with FEV1≥80% predicted and 10 subjects with uncontrolled asthma with FEV1 <80% predicted. BAL fluid was obtained from all subjects. The numbers of different cell types and the levels of 48 cytokines were measured in these fluids. Compared to healthy control subjects, patients with asthma had significantly more percentages of eosinophils and neutrophils, IL-1RA, IL-1α, IL-1β, IL-2Rα, IL-5, IL-6, IL-7, IL-8, G-CSF, GROα (CXCL1), MIP-1β (CCL4), MIG (CXCL9), RANTES (CCL5) and TRAIL in their BAL fluids. The only inflammatory markers that distinguished controlled asthma from uncontrolled asthma were neutrophil percentage and IL-8 levels, and both were inversely correlated with FEV1. We examined whether grouping asthma subjects on the basis of BAL eosinophil % or neutrophil % could identify specific cytokine profiles. The only differences between neutrophil-normal asthma (neutrophil≤2.4%) and neutrophil-high asthma (neutrophils%>2.4%) were a higher BAL fluid IL-8 levels, and a lower FEV1 in the latter group. By contrast, compared to eosinophil-normal asthma (eosinophils≤0.3%), eosinophil-high asthma (eosinophils>0.3%) had higher levels of IL-5, IL-13, IL-16, and PDGF-bb, but same neutrophil percentage, IL-8, and FEV1. Our results identify neutrophils and IL-8 are the only inflammatory components in BAL fluids that distinguish controlled asthma from uncontrolled asthma, and both correlate inversely with FEV1.

Highlights

  • Asthma is a complex chronic inflammatory disorder of the airways with a high prevalence rate of approximately 300 million people worldwide [1]

  • Building on the unexpected observation that % neutrophil but not % eosinophils correlated inversely with % predicted FEV1 in asthma, we examined whether grouping asthma subjects on the basis of bronchoalveolar lavage (BAL) eosinophil % or neutrophil % could identify specific cytokine profiles

  • By contrast, compared to Neu-Normal asthma, Neu-High asthma had higher IL-8 levels (p

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Summary

Introduction

Asthma is a complex chronic inflammatory disorder of the airways with a high prevalence rate of approximately 300 million people worldwide [1]. Severe asthma represents approximately 5 to 10% of all subjects with asthma [2], but accounts for 40% of the total cost for asthma care [2] and 30–50% of asthma morbidity [3]. The SARP study reported that the well-established biomarkers of asthma, such as blood eosinophils, serum IgE, and exhaled nitric oxide levels, do not differentiate asthma severity or correlate with FEV1 or asthma severity [4]. The RET/ATS guidelines have been changed for defining asthma severity to controlled and uncontrolled asthma. It is important to identify specific cytokines that distinguish uncontrolled asthma from controlled asthma in the new guideline to develop novel therapeutic targets for severe asthma

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