Project Details
Abstract
Asthma is a complex pulmonary inflammatory disease. It is generally believed that the susceptible
individuals have an abnormal immune response to inhaled allergens. According to some previous studies,
Th2 cells and their cytokines play pivotal roles in the pathogenesis of asthma. In addition, the activation of
the mast cells and eosinophils in the airway mucosa releases high levels of proinflammatory mediators
which induce bronchial obstruction, airway hyper-responsiveness, and airway inflammation. We have
established the hybrid adeno-associate virus (AAV) 2/9 vector system to carry siRNA specific to
eotaxin-1 (CCL11) and results showed efficient reduction of eosinophilia, airway hyperresponsiveness
(AHR) and local Th2 cytokine levels in allergen-sensitized mice. The cDNA sequence of Clara cell 10 kD
protein (CC10) was also constructed and had similar therapeutic effect as AAV-siCCL11. The activity of
inflammasomes has recently been reported to correlate with the pathogenesis of asthma, particular the
purinergic P2X7 receptor and its related molecules, include NLRP3, Pannexin-1, and IL-33. Therefore, we
will evaluate whether the expression of CC10 by AAV vector would reduce the inflammasome activity in
asthmatic mice. The AAV gene delivery systems will also target the inflammasome components, including
siRNA sequences to NLRP3, P2X7 receptor, Pannexin-1, or IL-33. Further, the expression of Pannexin-1
mimetic blocking peptide (10panx1) from epithelial cells will be examined. The airway
hyperresponsiveness, cell infiltration in BALF, ATP levels, and the expression of inflammasome molecules
will be determined. The results will offer a better understanding of the roles of inflammasome activity in
asthmatic pathogenesis. Some novel therapeutic approaches with those molecules will be developed, based
on the information obtained from this study.
Project IDs
Project ID:PC10108-0882
External Project ID:NSC101-2320-B182-033
External Project ID:NSC101-2320-B182-033
Status | Finished |
---|---|
Effective start/end date | 01/08/12 → 31/07/13 |
Fingerprint
Explore the research topics touched on by this project. These labels are generated based on the underlying awards/grants. Together they form a unique fingerprint.