Otitis media with effusion (OME) is one of the largest public health problems of young children. The inflammatory events that occur in OME lead to effusion and tissue hyperplasia that in turn can produce temporary and permanent hearing loss. Immune responses play a critical role in OME. Immunity is intimately involved in the host response to infection in the middle ear (ME), and provides the primary defense of the ME from infection. In addition, immune-mediated inflammation has been implicated in OME pathogenesis. In the current application, we propose to study the cellular and molecular mechanisms that control immunity and tissue proliferation in the ME. We will identify the endothelial cell receptors that control the recruitment of leukocytes into the ME cavity during OME, and determine whether these receptors can be inhibited. We will investigate cytokines that regulate the expression of systemic and local mucosal immunity in the ME, and explore procedures to increase the ME immune response to bacterial antigens. We will also identify the growth factors and receptors that are present in the ME mucosa during hyperplasia, and document their ability to stimulate cell proliferation in the mucosa both in vitro and in vivo. Finally, we will test inhibitors of growth factor receptors to determine whether mucosal hyperplasia can be ameliorated or reversed during OME.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC000129-21
Application #
2899993
Study Section
Hearing Research Study Section (HAR)
Project Start
1990-04-01
Project End
2000-06-30
Budget Start
1999-04-01
Budget End
2000-06-30
Support Year
21
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of California San Diego
Department
Surgery
Type
Schools of Medicine
DUNS #
077758407
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Kurabi, Arwa; Schaerer, Daniel; Chang, Lisa et al. (2018) Optimisation of peptides that actively cross the tympanic membrane by random amino acid extension: a phage display study. J Drug Target 26:127-134
Kurabi, Arwa; Schaerer, Daniel; Noack, Volker et al. (2018) Active Transport of Peptides Across the Intact Human Tympanic Membrane. Sci Rep 8:11815
Kurabi, Arwa; Beasley, Kerry A; Chang, Lisa et al. (2017) Peptides actively transported across the tympanic membrane: Functional and structural properties. PLoS One 12:e0172158
Deniffel, Dominik; Nuyen, Brian; Pak, Kwang et al. (2017) Otitis Media and Nasopharyngeal Colonization in ccl3-/- Mice. Infect Immun 85:
Cho, Chang Gun; Pak, Kwang; Webster, Nicholas et al. (2016) Both canonical and non-canonical NF-?B activation contribute to the proliferative response of the middle ear mucosa during bacterial infection. Innate Immun 22:626-634
Kurabi, Arwa; Pak, Kwang K; Bernhardt, Marlen et al. (2016) Discovery of a Biological Mechanism of Active Transport through the Tympanic Membrane to the Middle Ear. Sci Rep 6:22663
Hernandez, Michelle; Leichtle, Anke; Pak, Kwang et al. (2015) The transcriptome of a complete episode of acute otitis media. BMC Genomics 16:259
Leichtle, Anke; Klenke, Christin; Ebmeyer, Joerg et al. (2015) NOD-Like Receptor Signaling in Cholesteatoma. Biomed Res Int 2015:408169
Kurabi, Arwa; Lee, Jasmine; Wong, Chelsea et al. (2015) The inflammasome adaptor ASC contributes to multiple innate immune processes in the resolution of otitis media. Innate Immun 21:203-14
Yao, William; Frie, Meredith; Pan, Jeffrey et al. (2014) C-Jun N-terminal kinase (JNK) isoforms play differing roles in otitis media. BMC Immunol 15:46

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