The natural history of chronic HCV infection is very variable and retrospective studies have identified both slow progressors who take 40 years to develop cirrhosis and rapid progressors who may develop advanced fibrosis in as little as 10 - 20 years. The underlying pathophysiological mechanisms associated with disease progression are poorly understood and represent the central focus of this HCV Center. We will study cohorts of patients with variable rates of disease progression. The Clinical Center for HCV disease progression will provide liver tissues, specimens, clinical expertise, biostatistics and a pathology core to interact with the basic Investigators in this HCV Center proposal. The clinical center will utilize both existing cohorts and develop novel cohorts of patients with either slow or fast disease progression to study the underlying immunological, virological and metabolic factors associated with progression of liver fibrosis. In particular we will develop: 1) the Infrastructure for clinical investigation into mechanisms of disease progression and fibrosis in patients with HCV 2) Evaluation of 4 distinct cohorts of patients who have variable rates of fibrosis progression: A) Patients with HCV naive to treatment representing a control group of predominantly slow progressors B) Patients with HCV and Schistosomiasis who rapidly develop cirrhosis C) Patients with HIV/HCV; a subset of whom are immunocompromised with low CD4 counts and may progress more rapidly D) Patients post liver transplant who have recurrent HCV These studies may help identify the mechanism of fibrosis progression and lead to rational use of reources to identify and treat patients at higher risk of disease progression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program--Cooperative Agreements (U19)
Project #
5U19AI066313-03
Application #
7385106
Study Section
Special Emphasis Panel (ZAI1)
Project Start
Project End
Budget Start
2007-03-01
Budget End
2008-02-29
Support Year
3
Fiscal Year
2007
Total Cost
$74,126
Indirect Cost
Name
Beth Israel Deaconess Medical Center
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02215
Kim, Yong Ook; Popov, Yury; Schuppan, Detlef (2017) Optimized Mouse Models for Liver Fibrosis. Methods Mol Biol 1559:279-296
Locatelli, Luigi; Cadamuro, Massimiliano; Spirlì, Carlo et al. (2016) Macrophage recruitment by fibrocystin-defective biliary epithelial cells promotes portal fibrosis in congenital hepatic fibrosis. Hepatology 63:965-82
Jiménez Calvente, Carolina; Sehgal, Alfica; Popov, Yury et al. (2015) Specific hepatic delivery of procollagen ?1(I) small interfering RNA in lipid-like nanoparticles resolves liver fibrosis. Hepatology 62:1285-97
Yang, Liu; Kwon, Junghee; Popov, Yury et al. (2014) Vascular endothelial growth factor promotes fibrosis resolution and repair in mice. Gastroenterology 146:1339-50.e1
Kwong, Gabriel A; von Maltzahn, Geoffrey; Murugappan, Gayathree et al. (2013) Mass-encoded synthetic biomarkers for multiplexed urinary monitoring of disease. Nat Biotechnol 31:63-70
Chowdhury, Sumaiya; Chen, Yiqian; Yao, Tsun-Wen et al. (2013) Regulation of dipeptidyl peptidase 8 and 9 expression in activated lymphocytes and injured liver. World J Gastroenterol 19:2883-93
Yanagisawa, K; Yue, S; van der Vliet, H J et al. (2013) Ex vivo analysis of resident hepatic pro-inflammatory CD1d-reactive T cells and hepatocyte surface CD1d expression in hepatitis C. J Viral Hepat 20:556-65
Schuppan, Detlef; Pinzani, Massimo (2012) Anti-fibrotic therapy: lost in translation? J Hepatol 56 Suppl 1:S66-74
Lynch, Lydia; Nowak, Michael; Varghese, Bindu et al. (2012) Adipose tissue invariant NKT cells protect against diet-induced obesity and metabolic disorder through regulatory cytokine production. Immunity 37:574-87
Li, Shaoyong; Vriend, Lianne E M; Nasser, Imad A et al. (2012) Hepatitis C virus-specific T-cell-derived transforming growth factor beta is associated with slow hepatic fibrogenesis. Hepatology 56:2094-105

Showing the most recent 10 out of 25 publications