This is a renewal application of two years of the R01 grant funded by NIH American Recovery Reinvestment Act (ARRA). This grant had been funded from July 15, 2009 to June 30, 2011 and has led to a series of fundamental principles concerning the role of Interleukin 15 (IL-15) in EE pathogenesis. This renewal application seeks to extend our basic and translational analysis of EE, aimed at providing the role of IL-15 and IL-15 responsive cells in the regulation of esophageal eosinophilia in human EE. In the first cycle of the two- year R01 grant funding, we identified several key molecules that are responsible for the initiation and progression of EE pathogenesis in experimental models and have developed evidence that these findings apply to human EE. The details of our findings are presented in the progress report. In brief, we have demonstrated that induced mRNA/protein of IL-15 and iNKT cells in the esophageal biopsies of humans EE and provided evidence that IL-15 and iNKT cells have a critical role in the initiation and progression of aeroallergen or food allergen (peanut)-induced experimental EE. IL-15 has been identified as an important player in allergic immune responses;it mediates diverse biological responses, ranging from proliferation and differentiation. Antigen presenting cell-derived IL15 stimulates the proliferation of naive and CD8+ T cells, iNKT cells and enhances the differentiation of naive T cells towards a Th2 phenotype in the presence of IL4. Additionally, we present preliminary data that it activates B cells and induces IgE. Therefore, in the extended cycle of grant tenure, we propose to test the central hypothesis that chronic IL-15 expression leads to the development of IgE-associated EE pathogenesis and that the surface molecules of IL-15, IL-15-responsive cells, chemokines, and mediators are the potential diagnostic and therapeutic target molecules for human EE. The three specific aims will test our central hypothesis. In the first aim, we will test several sub-hypotheses by examining esophageal transcript profile of IL-15 overexpressed mice, role of IL-15 in the induction of mast cells and B cell growth, activation, and proliferation and the mechanism of Ig class switching in EE. A correlation of IL-15 will also be examined for the development of esophageal furrows, rings, and stricture in human EE.
The second aim will test the hypothesis that IL-15 and the cell surface molecules and chemokines of IL-15-responsive cells may be novel diagnostic biomarkers for human EE. We will test several related sub-hypotheses concerning the mRNA and protein levels of IL-15, IL-15R?, IgE, CD1d, V?24, and chemokines CXCL16 in the blood of normal individuals, gastroesophageal reflux disease (GERD) and EE patients. In the third aim, we propose a set of experiments designed to test several related primary hypotheses focused around iNKT cells and IL-15 being novel target molecules for EE therapy. Our studies are timely given the recent attention that EE is receiving in the medical community.

Public Health Relevance

Eosinophilic esophagitis (EE) is a recently recognized inflammatory esophageal disorder with increasing prevalence;however, the etiology of the disease pathogenesis is yet not clearly understood. The goal of the present proposal is to establish a novel mechanistic pathway based on IL-15 overexpression in the esophagus and provide novel noninvasive diagnostic biomarkers and therapeutic target molecules for EE.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI080581-05
Application #
8656079
Study Section
Gastrointestinal Mucosal Pathobiology Study Section (GMPB)
Program Officer
Minnicozzi, Michael
Project Start
2009-07-22
Project End
2018-04-30
Budget Start
2014-05-01
Budget End
2015-04-30
Support Year
5
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Tulane University
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
New Orleans
State
LA
Country
United States
Zip Code
70118
Venkateshaiah, Sathisha Upparahalli; Zhu, Xiang; Rajavelu, Priya et al. (2017) Regulatory effects of IL-15 on allergen-induced airway obstruction. J Allergy Clin Immunol :
Manohar, Murli; Verma, Alok Kumar; Venkateshaiah, Sathisha Upparahalli et al. (2017) Pathogenic mechanisms of pancreatitis. World J Gastrointest Pharmacol Ther 8:10-25
Manohar, Murli; Kumar Verma, Alok; Upparahalli Venkateshaiah, Sathisha et al. (2017) Role of eosinophils in the initiation and progression of pancreatitis pathogenesis. Am J Physiol Gastrointest Liver Physiol :ajpgi002102017
Manohar, Murli; Verma, Alok K; Upparahalli Venkateshaiah, Sathisha et al. (2017) Food-Induced Acute Pancreatitis. Dig Dis Sci 62:3287-3297
Verma, Alok K; Manohar, Murli; Upparahalli Venkateshaiah, Sathisha et al. (2017) Neuroendocrine cells derived chemokine vasoactive intestinal polypeptide (VIP) in allergic diseases. Cytokine Growth Factor Rev 38:37-48
Sanders, Nathan L; Mishra, Anil (2016) Role of interleukin-18 in the pathophysiology of allergic diseases. Cytokine Growth Factor Rev 32:31-39
Venkateshaiah, Sathisha Upparahalli; Manohar, Murli; Verma, Alok K et al. (2016) Possible Noninvasive Biomarker of Eosinophilic Esophagitis: Clinical and Experimental Evidence. Case Rep Gastroenterol 10:685-692
Davis, Benjamin P; Rothenberg, Marc E (2016) Mechanisms of Disease of Eosinophilic Esophagitis. Annu Rev Pathol 11:365-93
Rothenberg, Marc E (2015) Molecular, genetic, and cellular bases for treating eosinophilic esophagitis. Gastroenterology 148:1143-57
Shukla, Anshi; Mishra, Akanksha; Venkateshaiah, Sathisha Upparahalli et al. (2015) Elements Involved In Promoting Eosinophilic Gastrointestinal Disorders. J Genet Syndr Gene Ther 6:

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