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Increased Muc5AC and Decreased Ciliated Cells in Severe Asthma Partially Restored by Inhibition of IL-4Rα Receptor.
Boomer, Jonathan; Choi, Jiwoong; Alsup, Alexander; McGregor, Mary Clare; Lieu, Julia; Johnson, Cooper; Hall, Chase; Shi, Xiaosong; Kim, Taewon; Goss, Charles; Lew, Daphne; Christenson, Stephanie; Woodruff, Prescott G; Hastie, Annette; Mauger, David; Wenzel, Sally E; Hoffman, Eric A; Schechtman, Ken B; Castro, Mario.
Afiliação
  • Boomer J; University of Kansas School of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Kansas City, Kansas, United States.
  • Choi J; University of Kansas School of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Kansas City, Kansas, United States.
  • Alsup A; University of Kansas School of Medicine, Pulmonary, Critical Care and Sleep Medicine , Kansas City, Kansas, United States.
  • McGregor MC; Washington University in St Louis School of Medicine, Division of Pulmonary and Critical Care Medicine, St Louis, Missouri, United States.
  • Lieu J; Washington University in St Louis School of Medicine, Division of Pulmonary and Critical Care Medicine , St Louis, Missouri, United States.
  • Johnson C; Washington University School of Medicine in Saint Louis, Pulmonary/Critical Care Medicine, St Louis, Missouri, United States.
  • Hall C; University of Kansas School of Medicine, Pulmonary Medicine and Critical Care, Kansas City, Kansas, United States.
  • Shi X; University of Kansas School of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Kansas City, Kansas, United States.
  • Kim T; University of Kansas School of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Kansas City, Kansas, United States.
  • Goss C; Washington University in Saint Louis School of Medicine, Biostatistics, Saint Louis, Missouri, United States.
  • Lew D; Washington University in Saint Louis School of Medicine, Biostatistics, Saint Louis, Missouri, United States.
  • Christenson S; University of California San Francisco, Pulmonary & Critical Care, San Francisco, California, United States.
  • Woodruff PG; University of California San Francisco, Division of Pulmonary and Critical Care Medicine, Department of Medicine and CVRI, San Francisco, California, United States.
  • Hastie A; Wake Forest School of Medicine, Center for Genomics and Personalized Medicine Research, School of Medicine, Winston-Salem, North Carolina, United States.
  • Mauger D; Pennsylvania State University, Division of Statistics and Bioinformatics, Department of Public Health Sciences, , Hershey, Pennsylvania, United States.
  • Wenzel SE; University of Pittsburgh School of Medicine, Department of Environmental and Occupation Health, Pittsburgh, Pennsylvania, United States.
  • Hoffman EA; University of Iowa Hospitals and Clinics, 8Department of Radiology, Biomedical Engineering, and Medicine, Iowa City, Iowa, United States.
  • Schechtman KB; Washington University in Saint Louis, Biostatistics, Saint Louis, Missouri, United States.
  • Castro M; University of Kansas School of Medicine, Pulmonary, Critical Care and Sleep Medicine, Kansas City, Kansas, United States; mcastro2@kumc.edu.
Article em En | MEDLINE | ID: mdl-38935626
ABSTRACT

BACKGROUND:

The role of IL-13 on the airway epithelium in severe asthma leading to airway remodeling remains poorly understood.

OBJECTIVE:

To study IL-13 induced airway remodeling on goblet cells and cilia in the airway epithelium in severe asthma and the impact of an anti-IL4Rα antibody, dupilumab, in vitro.

METHODS:

Quantitative CT (qCT) lungs and endobronchial biopsies and brushings were obtained in 51 participants (22 severe, 11 non-severe asthma and 18 healthy participants) in the Severe Asthma Research Program (SARPIII) and measured for mucin and cilia related proteins. Epithelial cells were differentiated in air-liquid interphase (ALI) with IL-13 +/-dupilumab and assessed for mucin, cilia, cilia beat frequency (CBF) and epithelial integrity (transepithelial electrical resistance, TEER).

RESULTS:

Increased Muc5AC (Δ+263.2±92.7 lums/EpiArea) and decreased ciliated cells (Δ-0.07±0.03 Foxj1+cells/EpiArea) were observed in biopsies from severe asthma when compared to healthy (p<0.01 and p=0.047 respectively). RNAseq of epithelial cell brushes confirmed a Muc5AC increase with a decrease in a 5-gene cilia-related mean in severe asthma compared to healthy (all p<0.05). IL-13 (5 ng/mL) differentiated ALI cultures of healthy and asthmatic (severe and non-severe participants) increased Muc5AC, decreased cilia (α-acytl-tubulin) in healthy (Δ+6.5±1.5%, Δ-14.1±2.7%; all p<0.001 respectively) and asthma (Δ+4.4±2.5%, Δ-13.1±2.7%; p=0.084, p<0.001 respectively); decreased epithelial integrity (TEER) in healthy (-140.9±21.3 [ohms], p<0.001) while decreasing CBF in asthma (Δ-4.4±1.7 [Hz], p<0.01). When dupilumab was added to ALI with IL-13, there was no significant decrease in Mu5AC but there was restoration of cilia in healthy and asthma participants (absolute increase of 67.5% and 32.5% cilia, all p<0.05 respectively) while CBF increased (Δ+3.6±1.1 [Hz], p<0.001) and TEER decreased (only in asthma Δ-37.8±16.2 [ohms] p<0.05).

CONCLUSIONS:

IL-13 drives features of airway remodeling in severe asthma which are partially reversed by inhibiting IL-4Rα receptor in vitro.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article