Comprehensive longitudinal analysis of hepatitis C virus (HCV)‐specific T cell responses during acute HCV infection in the presence of existing HIV‐1 infection |
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Authors: | C. H. S. B. Van Den Berg T. A. Ruys N. M. Nanlohy S. E. Geerlings J. T. Van Der Meer J.‐W. Mulder J. A. Lange D. Van Baarle |
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Affiliation: | 1. Department of Experimental Virology, Center for Infection and Immunity (CINIMA), Academic Medical Center, Amsterdam, the Netherlands;2. Cluster of Infectious Diseases, Department of Research, Amsterdam Health Service, Amsterdam, the Netherlands;3. Department of Immunology, University Medical Center Utrecht, Utrecht, the Netherlands;4. Both authors contributed equally to this paper.;5. International Antiviral Therapy and Evaluation Center (IATEC), CINIMA, Academic Medical Center, Amsterdam, the Netherlands;6. Department of Internal Medicine, Division of Infectious Diseases, Tropical Medicine and AIDS, CINIMA, Academic Medical Center, Amsterdam, the Netherlands;7. Department of Internal Medicine, Slotervaart Hospital, Amsterdam, the Netherlands;8. Department of Internal Medicine, University Medical Center Utrecht, Utrecht, the Netherlands |
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Abstract: | Summary. The aim of this study was to study the development of HCV‐specific T cell immunity during acute HCV infection in the presence of an existing HIV‐1 infection in four HIV‐1 infected men having sex with men. A comprehensive analysis of HCV‐specific T cell responses was performed at two time points during acute HCV infection using a T cell expansion assay with overlapping peptide pools spanning the entire HCV genome Three patients with (near) normal CD4+ T cell counts (range 400–970 × 106/L) either resolved (n = 1) or temporary suppressed HCV RNA. In contrast, one patient with low CD4+ T cell counts (330 × 106/L), had sustained high HCV RNA levels. All four patients had low HCV‐specific CD8+ T cell responses, and similar magnitudes of CD4+ T cell responses. Interestingly, individuals with resolved infection or temporary suppression of HCV‐RNA had HCV‐specific CD4+ T cell responses predominantly against nonstructural (NS) proteins. While the individual with high HCV RNA plasma concentrations had CD4+ T cell responses predominantly directed against Core. Our data show that an acute HCV infection in an HIV‐1 infected person can be suppressed in the presence of HCV‐specific CD4+ T cell response targeting non‐structural proteins. However further research is needed in a larger group of patients to evaluate the role of HIV‐1 on HCV‐specific T cell responses in relation to outcome of acute HCV infection. |
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Keywords: | acute viral infection CD4+ T cells CD8+ T cells CTL HCV HIV‐1 immunology |
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