Hepatitis C virus (HCV) is a major health problem affecting approximately 200 million throughout the world. Although new therapies have improved the rates of sustained response, a large proportion of patients (~50%) fail to respond to antiviral treatment or develop significant drug toxicity, thus remaining at risk for disease progression. Thus, there is a pressing need for new preventative and therapeutic approaches, including vaccines. Understanding the viral evolutionary and immunologic events subsequent to HCV transmission, best assessed in the earliest stages of infection, is of direct relevance to vaccine design. However, acute HCV is often unrecognized because symptoms are usually mild or absent. We have established a large cohort of patients around the U.S. with acute HCV who we have followed longitudinally. In this proposal, we will examine mechanisms of CD8+ T cell escape, how functional attributes of these T cells influence the viral outcome of acute infection, and clone T cell receptors with optimal ability to recognize small amounts of peptide and mutant peptides. This will provide an important first step towards development of novel immunotherapeutic approaches.

Public Health Relevance

Hepatitis C virus (HCV) is an enormous health problem affecting 3% of the population. There is a pressing need for to understand the host immune and viral events early after infection in order to develop new treatments, including vaccines.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK060590-06A2
Application #
7594866
Study Section
Immunity and Host Defense Study Section (IHD)
Program Officer
Doo, Edward
Project Start
2002-09-15
Project End
2011-08-31
Budget Start
2009-09-01
Budget End
2010-08-31
Support Year
6
Fiscal Year
2009
Total Cost
$465,410
Indirect Cost
Name
University of Colorado Denver
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
041096314
City
Aurora
State
CO
Country
United States
Zip Code
80045
Golden-Mason, Lucy; Rosen, Hugo R (2013) Natural killer cells: multifaceted players with key roles in hepatitis C immunity. Immunol Rev 255:68-81
Rosen, Hugo R (2013) Emerging concepts in immunity to hepatitis C virus infection. J Clin Invest 123:4121-30
Golden-Mason, Lucy; Cox, Andrea L; Randall, Jessica A et al. (2010) Increased natural killer cell cytotoxicity and NKp30 expression protects against hepatitis C virus infection in high-risk individuals and inhibits replication in vitro. Hepatology 52:1581-9
Mengshol, John A; Golden-Mason, Lucy; Arikawa, Tomohiro et al. (2010) A crucial role for Kupffer cell-derived galectin-9 in regulation of T cell immunity in hepatitis C infection. PLoS One 5:e9504
McMahan, Rachel H; Golden-Mason, Lucy; Nishimura, Michael I et al. (2010) Tim-3 expression on PD-1+ HCV-specific human CTLs is associated with viral persistence, and its blockade restores hepatocyte-directed in vitro cytotoxicity. J Clin Invest 120:4546-57
Hurtado, Christine Waasdorp; Golden-Mason, Lucy; Brocato, Megan et al. (2010) Innate immune function in placenta and cord blood of hepatitis C--seropositive mother-infant dyads. PLoS One 5:e12232
Zhang, Yi; Liu, Yeuying; Moxley, Kelly M et al. (2010) Transduction of human T cells with a novel T-cell receptor confers anti-HCV reactivity. PLoS Pathog 6:e1001018
Eberlein, Jens; Nguyen, Tom T; Victorino, Francisco et al. (2010) Comprehensive assessment of chemokine expression profiles by flow cytometry. J Clin Invest 120:907-23
Cox, Andrea L; Page, Kimberly; Bruneau, Julie et al. (2009) Rare birds in North America: acute hepatitis C cohorts. Gastroenterology 136:26-31
Cummings, Kara L; Rosen, Hugo R; Hahn, Young S (2009) Frequency of gC1qR+CD4+ T cells increases during acute hepatitis C virus infection and remains elevated in patients with chronic infection. Clin Immunol 132:401-11

Showing the most recent 10 out of 27 publications