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Updated: Jul 8, 2026

Bronchial Thermoplasty: A Novel Therapeutic Approach to Severe Asthma
Published on: November 4, 2010
Exploring the potential efficacy of Ziziphus spina-christi on restoring steroid sensitivity in severe asthma
Narjes Saheb Sharif-Askari1, Baraa Khalid Salah Al-Sheakly2, Bushra Mdkhana2
1Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, United Arab Emirates; Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Objective:
To determine whether Ziziphus spina-christi adjuvant restores steroid hyporesponsiveness in severe asthma by strengthening the gut epithelial barrier and inhibiting the STING sensing pathway.
Methods:
Chemical profiling of Z. spina-christi extract was performed using liquid chromatography mass spectrometry (LC/MS-MS). Steroid-hyporesponsive asthma was induced with house dust mite (HDM) and cyclic-di-GMP (c-di-GMP). Mice were treated with dexamethasone, Z. spina-christi, or combination therapy. The study assessed gut histopathology, epithelial tight junction proteins, lung inflammation, airway hyporesponsiveness, inflammatory phenotypes, STING pathway activation, and glucocorticoid response.
Results:
Z. spina-christi exhibited a flavonoid-dominated chemotype enriched in quercetin-related compounds. Severe asthma induction was associated with significant gut epithelial injury, loss of tight junction proteins, and barrier dysfunction. Dexamethasone monotherapy failed to restore gut architecture or tight junction integrity. Conversely, Z. spina-christi markedly improved gut histology and reinstated expression of Claudin-1, Occludin, and ZO-1, with near-complete normalization observed with combination therapy. Restoring the gut barrier was associated with decreased airway inflammation, improved lung function, suppression of the STING pathway, and normalization of the GRα/GRβ ratio.
Conclusion:
Z. spina-christi enhances steroid sensitivity in severe asthma by restoring the gut epithelial barrier and reducing STING-driven inflammation.
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