4.7 Article

Mucociliary Clearance Differs in Mild Asthma by Levels of Type 2 Inflammation

Journal

CHEST
Volume 160, Issue 5, Pages 1604-1613

Publisher

ELSEVIER
DOI: 10.1016/j.chest.2021.05.013

Keywords

asthma; cilia; lung imaging; mucociliary clearance; mucus; scintigraphy; type 2 inflammation

Funding

  1. National Heart, Lung, and Blood Institute (NHLBI) [1R01 HL112863-01]

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This study investigates the influence of type 2 inflammation on mucus clearance rates in patients with mild asthma. The results indicate that patients with lower levels of type 2 inflammation have higher MCC and lower FENO levels, while those with higher levels of type 2 inflammation show significant variations in MCC, with some having low to zero clearance rates.
BACKGROUND: Although mucus plugging is a well-reported feature of asthma, whether asthma and type 2 inflammation affect mucociliary clearance (MCC) is unknown. RESEARCH QUESTION: Does type 2 inflammation influence mucus clearance rates in patients with mild asthma who are not receiving corticosteroids? STUDY DESIGN AND METHOD: The clearance rates of inhaled radiolabeled particles were compared between patients with mild asthma with low (n = 17) and high (n = 18) levels of T2 inflammation. Fraction exhaled nitric oxide (FENO) was used to prospectively segregate subjects into T2 Lo (FENO < 25 ppb) and T2 Hi (FENO > 35 ppb) cohorts. Bronchial brush samples were collected with fiber-optic bronchoscopy, and quantitative polymerase chain reaction was performed to measure expression of genes associated with T2 asthma. MCC rate comparisons were also made with a historical group of healthy control subjects (HCs, n = 12). RESULTS: The T2 Lo cohort demonstrated increased MCC when compared with both T2 Hi and historic HCs. MCC within the T2 Hi group varied significantly, with some subjects having low or zero clearance. MCC decreased with increasing expression of several markers of T2 airway inflammation (CCL26, NOS2, and POSTN) and with FENO. MUC5AC and FOXJ1 expression was similar between the T2Lo and T2Hi cohorts. INTERPRETATION: Increasing T2 inflammation was associated with decreasing MCC. High rates of MCC in T2 Lo subjects may indicate a compensatory mechanism present in mild disease but lost with high levels of inflammation. Future studies are required to better understand mechanisms and whether impairments in MCC in more severe asthma drive worse clinical outcomes.

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