Potential Treatment Alternatives and an Illustrative Case Study of Celiac Disease

Loading...
Thumbnail Image

Authors

Williams, Colt Jonas

Issue Date

2013

Type

Thesis

Language

en_US

Keywords

Research Projects

Organizational Units

Journal Issue

Alternative Title

Abstract

Celiac disease (CD) has taken center stage in the public eye, now afflicting 1:250 to 1:100 people in the United States. While CD etiology is most certainly polyfactorial, stemming from genetic, environmental, and immunologic factors, a causative agent of CD has been identified as a malfunctioning tissue transglutaminase (tTG). A ubiquitous enzyme that has numerous roles body-wide, tTG most notably digests small peptides in the jejunum. When tTG in the brush border of the small intestine comes in contact with gliadin, the immunoreactive peptide segment within gluten, tTG forms an irreversible complex that signals for an immune and inflammatory response. Current treatment options are limited only to strict adherence to a gluten free diet�"a lifestyle that is incompatible with the majority of the American population. I propose a radical treatment alternative, involving the silencing of the gene responsible for the faulty tTG. Using ß-cyclodextrin nanopolymers designed by Davis, et al. as a delivery vehicle, siRNA will be injected intravenously and specifically target small intestinal cells expressing tTG. An exemplary case study of a 23 year old female is included in order to illustrate possible celiac pathology and presentation.

Description

The University of Nevada, Reno Libraries will promptly respond to removal requests related to content that violates intellectual property laws, data protections, or has been uploaded without creator consent. Takedown notices should be directed to our ScholarWolf team (scholarwolf@library.unr.edu) with information about the object, including its full URL and the nature of your complaint.

Citation

Publisher

License

In Copyright(All Rights Reserved)

Journal

Volume

Issue

PubMed ID

DOI

ISSN

EISSN