Cellular Immune Responses in Seronegative Sexual Contacts of Acute Hepatitis C Patients

Author:

Kamal Sanaa M.123,Amin Ashraf2,Madwar Mohamed2,Graham Camilla S.1,He Qi1,Al Tawil Ahmed4,Rasenack Jens3,Nakano Tatsunori56,Robertson Betty5,Ismail Alaa2,Koziel Margaret James1

Affiliation:

1. Department of Infectious Diseases of Beth Israel Deaconess Medical Center and Harvard Medical School, Harvard Institutes of Medicine, Boston, Massachusetts

2. Department of Gastroenterology and Liver Diseases

3. Department of Internal Medicine II, Gastroenterology and Hepatology, University of Freiburg, Freiburg, Germany

4. Department of Pathology, Ain Shams Faculty of Medicine, Heliopolis, Cairo, Egypt

5. Division of Viral Hepatitis, Centers for Disease Control and Prevention, Atlanta, Georgia

6. Department of Internal Medicine, Ichinomiya Nishi Hospital, Ichinomiya, Aichi, Japan

Abstract

ABSTRACT Acute hepatitis C virus (HCV) is typically defined as new viremia and antibody seroconversion. Rates and immunologic correlates of hepatitis C clearance have therefore been based on clearance of viremia only in individuals who initially had an antibody response. We sought to characterize the immunological correlates of clearance in patients with acute hepatitis C and their sexual contacts. We prospectively determined CD4 + and CD8 + cytotoxic T-lymphocyte responses in index patients with acute HCV and their sexual contacts who developed acute infection, either with or without spontaneous clearance, as well as those contacts who never developed viremia. Responses were measured using proliferation and ELISpot assays for CD4 + and CD8 + responses. We demonstrate in this prospective study that cellular immune responses can develop in exposed but persistently aviremic and antibody-negative individuals as well as those individuals with spontaneous clearance of acute HCV. These findings lend further credence to the importance of cellular immune responses in recovery from HCV and suggest that low exposure to HCV may lead to development of HCV-specific immune responses without ongoing HCV replication. This finding has important implications for HCV vaccine and therapeutic development.

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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