Hepatitis C virus is both difficult to treat and a significant cause of morbidity and mortality. It is not understood how hepatitis C establishes infection nor how some patients clear infection. To this end 83 humans exposed to hepatitis C were studied in protocol 00-DK-0221. The immune response (both antibody and T cell) was closely followed and is being characterized. The study is in collaboration with Dr. Rehermann. It was found that some patients who were exposed to hepatitis C but did not develop overt infection (anti-HCV and HCV PCR negative) developed T-cell responses to hepatitis C. What was of particular interest was that some of the T-cell responses were directed at non-structural proteins. This would imply that there was subclinical viral replication and that more patients were in fact infected than one would expect based on traditional markers of infection. These patients managed to then clear the virus spontaneously. This work has now been completed and is published in two manuscripts. The first detailing the T cell responses (in press) and the second detailing the NK cell responses (published). To further understand the virological determinants of infection and the development of chronicity, the hepatitis C virus sequence in the early stages of infection has been determined from the same patients. In particular the sequencing effort is focused on the viral sequence before and after treatment, in the two patients who were HIV positive and relapsed. The complete sequence has been determined and is now being analyzed. A second laboraratory project has been to study the nature of late relapse after treatment for hepatitis C. The first 103 patients who achieved a sustained virologic response at the National Institutes of Health Clinical Center were reviewed. Three patients had a late relapse. The viral sequence from these patients was studied from before treatment, from the liver at the time of sustained virologic response, and from the serum at the time of documented relapse. The viral sequences obtained from before treatment, the liver at the time of sustained virologic response, and from the serum at the time of relapse were all virtually identical proving relapse and not reinfection. This manuscript is now in press. A third laboratory project has been completed and used viral sequencing to understand discrepancies in commercial genotyping assays. This is now published. A second type of chronic hepatitis studied is hepatitis D. Hepatitis D is the most aggressive form of viral hepatitis as well as the most difficult to treat. Interferon therapy is the standard approach. Patients are typically treated for 6 months to a year. Relapse after cessation of therapy is the norm. In protocol 01-DK-0247 patients are treated with peginterferon for 5 years. The dose is titrated to maintain normal ALT and minimize side effects. Thirteen patients were enrolled, and of the 12 who have had one-year evaluations 10 have met the protocol definition of response. 3/13 patients (27%) lost HBsAg after 24, 37 and 202 weeks of treatment and developed HBs antibodies. Treatment was stopped in these patients at least 24 weeks later;the serological response was durable and was associated with persistent improvement of ALT and platelet count during follow-up. Two patients (15%) died during therapy, one from hepatocellular carcinoma and the other from herpes colitis. Both deaths were not considered related to treatment. There were no other serious adverse events and treatment was well-tolerated overall. 3 patients required a dose reduction due to cytopenias. The primary end point of the study is the evaluation after three years although it is planned to treat patients for 5 years. Hepatitis D viral RNA and hepatitis B surface antigen levels have been measured and the final analysis has been completed. This work is now being prepared for publication. In addition the viral kinetics noted during response are being analyzed. A second treatment trial for hepatitis D has been initiated with a prenylation inhibitor. The first phase of this study has been completed with 8 patients enrolled and the second phase is now beginning enrollment. A new project has been commenced looking at inflammatory markers and there association with liver disease progression in a cohort of patients with chronic hepatitis C.

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Guedj, Jeremie; Rotman, Yaron; Cotler, Scott J et al. (2014) Understanding early serum hepatitis D virus and hepatitis B surface antigen kinetics during pegylated interferon-alpha therapy via mathematical modeling. Hepatology 60:1902-10
Heller, T; Rotman, Y; Koh, C et al. (2014) Long-term therapy of chronic delta hepatitis with peginterferon alfa. Aliment Pharmacol Ther 40:93-104
Sakiani, Sasan; Koh, Christopher; Heller, Theo (2014) Understanding the Presence of False-Positive Antibodies in Acute Hepatitis. J Infect Dis :
Hara, Koji; Rivera, Maria M; Koh, Christopher et al. (2014) Sequence analysis of hepatitis C virus from patients with relapse after a sustained virological response: relapse or reinfection? J Infect Dis 209:38-45
Harouni, Ahmed A; Gharib, Ahmed M; Osman, Nael F et al. (2014) Assessment of liver fibrosis using fast strain-encoded MRI driven by inherent cardiac motion. Magn Reson Med :
Rotman, Yaron; Noureddin, Mazen; Feld, Jordan J et al. (2014) Effect of ribavirin on viral kinetics and liver gene expression in chronic hepatitis C. Gut 63:161-9
Tana, Michele M; Heller, Theo (2013) Autoantibodies in hepatitis C: red flag or bystander effect? J Pediatr Gastroenterol Nutr 56:243
Heller, Theo; Werner, Jens Martin; Rahman, Fareed et al. (2013) Occupational exposure to hepatitis C virus: early T-cell responses in the absence of seroconversion in a longitudinal cohort study. J Infect Dis 208:1020-5
Werner, Jens Martin; Heller, Theo; Gordon, Ann Marie et al. (2013) Innate immune responses in hepatitis C virus-exposed healthcare workers who do not develop acute infection. Hepatology 58:1621-31
Fricker, Zachary; Levy, Elliot; Kleiner, David et al. (2013) Case series: biliary leak after transjugular liver biopsy. Am J Gastroenterol 108:145-7

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