Our goal is to dissect the mechanisms underlying the development of thyroiditis and diabetes in patients with chronic hepatitis C virus (HCV) infection in order to design new treatment and prevention modalities. Nearly 2.7 million individuals in the US have chronic hepatitis C, resulting in up to 13,000 deaths per year. Moreover, the prevalence of HCV infection is significantly higher among veterans;thus, chronic HCV is a major problem in VA hospitals. However, both HCV infection itself and its therapy (IFNa) frequently trigger thyroiditis and diabetes, thereby complicating the management of these patients. In the previous grant cycle, we made significant progress in dissecting the mechanisms by which thyroiditis and diabetes develop in HCV patients. We demonstrated that HCV and IFNa trigger thyroiditis by direct thyroid toxic effects and through epigenetic modifications in thyroiditis-susceptibility genes. In addition, we were able, for the first time, to infect human thyroid cells with HCV. Moreover, we recently discovered that IFNa also causes epigenetic changes in islet cells, suggesting a new mechanism for inducing diabetes in HCV patients (see Progress Report). In the current proposal, we will build on these findings and dissect the mechanisms by which HCV and IFNa trigger thyroiditis and diabetes. Our hypothesis is that patients with HCV infection treated with IFNa develop thyroiditis and/or diabetes due to direct epigenetic modifications of thyroiditis and diabetes-susceptibility genes in thyroid cells and islet beta cells, respectively.
Our specific aims are:
Specific Aim 1 : we will test in vitro genome-wide epigenetic modifications induced in human thyroid cells infected with HCV and exposed to IFNa;we will also evaluate epigenetic effects in the thyroid in vivo by creating a new transgenic mouse with tetracycline-inducible IFNa expression in the thyroid.
Specific Aim 2 : we will test the hypothesis that HCV and IFNa have direct toxic effects on beta cells through epigenetic modifications, causing diabetes in HCV-infected patients. In collaboration with Dr. Jason Blackard's group from UC, we will examine the epigenetic effects of exposure of a human beta cell line to HCV viral proteins or infectious virions, as well as the epigenetic modifications induce by IFNa in human beta cells.
Specific Aim 3 : we will test systemic effects of IFNa in other tissues, in addition to the thyroid and pancreas, by treating mice with IFNa systemically, and examining its effects on global methylation, histone modifications, and miR expression in selected tissues (blood, liver, fat, and muscle). In summary, our proposed studies will dissect the molecular mechanisms causing thyroiditis and diabetes in chronic hepatitis C patients receiving IFNa. Chronic hepatitis C infection is a major health problem for veterans, and thyroiditis and diabetes are common co-morbid conditions in these patients that significantly interfere with effective treatment of chroni HCV. Understanding the etiology of thyroiditis and diabetes in chronic HCV patients will enable the development of novel treatment modalities and prevention strategies based on the mechanisms triggering diabetes and thyroiditis in these patients. These new prevention and treatment strategies for thyroiditis and diabetes in HCV patients will facilitate the treatment and cure of chronic hepatitis C in veterans and non-veterans.

Public Health Relevance

The goals of our study are to identify the mechanisms by which certain medications and viruses cause thyroiditis and diabetes. Our hypothesis is that viruses and medications cause epigenetic modifications (changes in gene regulation) in thyroiditis and diabetes susceptibility genes that trigger these diseases. We developed a unique multifaceted approach that will enable us to dissect the epigenetic effects of medications/viruses on the thyroid and the pancreatic beta cells, and to determine how they cause disease.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Non-HHS Research Projects (I01)
Project #
1I01BX002031-01
Application #
8442424
Study Section
Endocriniology A (ENDA)
Project Start
2013-01-01
Project End
2016-12-31
Budget Start
2013-01-01
Budget End
2013-12-31
Support Year
1
Fiscal Year
2013
Total Cost
Indirect Cost
Name
James J Peters VA Medical Center
Department
Type
DUNS #
040077133
City
Bronx
State
NY
Country
United States
Zip Code
10468
Blackard, Jason T; Kong, Ling; Lombardi, Angela et al. (2017) A preliminary analysis of hepatitis C virus in pancreatic islet cells. Virol J 14:237
Hammerstad, Sara Salehi; Stefan, Mihaela; Blackard, Jason et al. (2017) Hepatitis C Virus E2 Protein Induces Upregulation of IL-8 Pathways and Production of Heat Shock Proteins in Human Thyroid Cells. J Clin Endocrinol Metab 102:689-697
Lombardi, Angela; Inabnet 3rd, William Barlow; Owen, Randall et al. (2015) Endoplasmic reticulum stress as a novel mechanism in amiodarone-induced destructive thyroiditis. J Clin Endocrinol Metab 100:E1-10
Stefan, Mihaela; Zhang, Weijia; Concepcion, Erlinda et al. (2014) DNA methylation profiles in type 1 diabetes twins point to strong epigenetic effects on etiology. J Autoimmun 50:33-7
Stefan, Mihaela; Wei, Chengguo; Lombardi, Angela et al. (2014) Genetic-epigenetic dysregulation of thymic TSH receptor gene expression triggers thyroid autoimmunity. Proc Natl Acad Sci U S A 111:12562-7
Hasham, Alia; Zhang, Weijia; Lotay, Vaneet et al. (2013) Genetic analysis of interferon induced thyroiditis (IIT): evidence for a key role for MHC and apoptosis related genes and pathways. J Autoimmun 44:61-70
Blackard, Jason T; Kong, Ling; Huber, Amanda K et al. (2013) Hepatitis C virus infection of a thyroid cell line: implications for pathogenesis of hepatitis C virus and thyroiditis. Thyroid 23:863-70
Stefan, Mihaela; Jacobson, Eric M; Huber, Amanda K et al. (2011) Novel variant of thyroglobulin promoter triggers thyroid autoimmunity through an epigenetic interferon alpha-modulated mechanism. J Biol Chem 286:31168-79