Dynamic Changes in Ex Vivo T-Cell Function After Viral Clearance in Chronic HCV Infection

Author:

Han Ji Won1,Sung Pil Soo123,Kim Kyung Hwan1,Hong Seon-Hui4,Shin Eui-Cheol14,Jun Song Myeong235,Park Su-Hyung14

Affiliation:

1. Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea

2. The Catholic University Liver Research Center, Department of Internal Medicine, College of Medicine, Daejeon, Republic of Korea

3. Division of Hepatology, Department of Internal Medicine, College of Medicine, Daejeon, Republic of Korea

4. Biomedical Science and Engineering Interdisciplinary Program, Korea Advanced Institute of Science and Technology, Daejeon, Republic of Korea

5. Daejeon St Mary’s Hospital, The Catholic University of Korea, Daejeon, Republic of Korea

Abstract

Abstract Background Direct-acting antiviral (DAA) agents can successfully treat chronic hepatitis C virus (HCV) infection. However, the ex vivo HCV-specific T-cell function following viral clearance remains unknown. Methods We investigated functional alterations and phenotypic changes in ex vivo HCV-specific CD8+ T cells with a longitudinal analysis of 41 patients with chronic HCV infection who were undergoing DAA treatment. Results A patient subset exhibited a significantly increased T-cell response (mainly CD8+ T cells) at week 4 of treatment. However, this increased T-cell response diminished in later weeks. Relative to pretreatment levels, the ex vivo HCV-specific CD8+ T-cell frequency decreased at 12 weeks after the end of treatment, along with a decreased antigen-experienced CD8+ T-cell population. DAA treatment increased the proliferative capacity of HCV-specific CD8+ T cells, but this change was not correlated with ex vivo function. Patients experiencing viral breakthrough or relapse exhibited defective restoration of T-cell function. Conclusion Our present results indicated that DAA-mediated viral clearance only transiently restored ex vivo T-cell function, suggesting a need to enhance T-cell function in DAA-treated patients.

Funder

Ministry of Health and Welfare, Republic of Korea

Catholic University of Korea

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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