Multiple studies by our investigative team and others demonstrate that prostaglandin E2 (PGE2) regulates the function of multiple cell types in the lung, including resident structural cells, nerves, and infiltrating blood cells. Although PGE2 has been shown to mediate numerous anti-inflammatory effects, it has also been shown to promote certain pro-inflammatory actions, as well as undesirable side effects, the most prominent being cough, that have stalled efforts to exploit its clinical potential. The numerous and complex effects of PGE2 are due, in large part, to the existence of 4 different EP receptor subtypes. Each of EP receptor subtypes (EP1, 2, 3, and 4) promotes different signaling and function when stimulated by PGE2, while being differentially expressed in the numerous cell types in the lung. The goal of this project is to take advantage of recent advances in EP receptor pharmacology and research capabilities, to identify the optimal EP receptor targeting strategy to treat asthma. Our central hypothesis is that EP receptors mediate a complex array of functions in the lung and in allergic lung inflammation, and selective targeting of EP subtypes can provide optimal therapy for asthma by ameliorating lung inflammation, airway hyperresponsiveness (AHR), and airway remodeling, while avoiding promotion of cough. We have assembled a multi-PI, international team capable of exhaustively characterizing EP subtype function, and the utility of EP targeting for the purpose of asthma therapy.
Three Aims will be pursued that constitute a robust analysis of the cooperative (positive and negative) roles of EP receptors in cell, tissue, and in vivo models.
Aim 1 will employ rodent models of allergic lung inflammation and assess the effect of multiple combinations of EP agonists and antagonists on lung inflammation, airway remodeling, and airway hyperresponsiveness.
Aim 2 will focus on EP receptor signaling and regulation of relevant human and rodent cell (airway smooth muscle, airway epithelia, and mast cells) functions.
Aim 3 will employ cell, tissue, and in vivo models to detail EP receptor regulation of cough. Upon conclusion of these studies we will have identified a novel therapeutic approach that has long been suspected but has eluded the research community for decades.

Public Health Relevance

Asthma is an obstructive lung disease affecting over 235 million people worldwide, of which up to 50% are not optimally managed. Studies proposed will seek to identify a new therapeutic strategy that targets specific (prostaglandin) receptors that are expressed on many lung cell types. Because these receptors have the capability of regulating all 3 major features of asthma (lung inflammation, remodeling, and excessive airway closure), this strategy is predicted to be superior to current drugs used for treating asthma.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL136209-02
Application #
9418090
Study Section
Lung Cellular, Molecular, and Immunobiology Study Section (LCMI)
Program Officer
Noel, Patricia
Project Start
2017-02-01
Project End
2021-01-31
Budget Start
2018-02-01
Budget End
2019-01-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Thomas Jefferson University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
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Cahill, Katherine N; Katz, Howard R; Cui, Jing et al. (2017) KIT Inhibition by Imatinib in Patients with Severe Refractory Asthma. N Engl J Med 376:1911-1920
Liu, Tao; Barrett, Nora A; Kanaoka, Yoshihide et al. (2017) Type 2 Cysteinyl Leukotriene Receptors Drive IL-33-Dependent Type 2 Immunopathology and Aspirin Sensitivity. J Immunol :
Cahill, Katherine N; Raby, Benjamin A; Zhou, Xiaobo et al. (2016) Impaired E Prostanoid2 Expression and Resistance to Prostaglandin E2 in Nasal Polyp Fibroblasts from Subjects with Aspirin-Exacerbated Respiratory Disease. Am J Respir Cell Mol Biol 54:34-40