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Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C

Authors :
Tina Senff
Christopher Menne
Christine Cosmovici
Lia Laura Lewis-Ximenez
Jasneet Aneja
Ruth Broering
Arthur Y. Kim
Astrid M. Westendorf
Ulf Dittmer
Norbert Scherbaum
Georg M. Lauer
Jörg Timm
Source :
JCI Insight, Vol 7, Iss 2 (2022)
Publication Year :
2022
Publisher :
American Society for Clinical investigation, 2022.

Abstract

Invariant NK T (iNKT) cells are implicated in viral clearance; however, their role in hepatitis C virus (HCV) infection remains controversial. Here, iNKT cells were studied during different stages of HCV infection. iNKT cells from patients with acute HCV infection and people who inject drugs (PWID) with chronic or spontaneously resolved HCV infection were characterized by flow cytometry. In a longitudinal analysis during acute HCV infection, frequencies of activated CD38+ iNKT cells reproducibly declined in spontaneously resolving patients, whereas they were persistently elevated in patients progressing to chronic infection. During the first year of infection, the frequency of activated CD38+ or CD69+ iNKT cells strongly correlated with alanine transaminase levels with particularly pronounced correlations in spontaneously resolving patients. Increased frequencies of activated iNKT cells in chronic HCV infection were confirmed in cross-sectional analyses of PWID with chronic or spontaneously resolved HCV infection; however, no apparent functional differences were observed with various stimulation protocols. Our data suggest that iNKT cells are activated during acute hepatitis C and that activation is sustained in chronic infection. The correlation between the frequency of activated iNKT cells and alanine transaminase may point toward a role of iNKT cells in liver damage.

Subjects

Subjects :
Immunology
Virology
Medicine

Details

Language :
English
ISSN :
23793708 and 76439984
Volume :
7
Issue :
2
Database :
Directory of Open Access Journals
Journal :
JCI Insight
Publication Type :
Academic Journal
Accession number :
edsdoj.2ce0e1d8a7643998475de34972c062b
Document Type :
article
Full Text :
https://doi.org/10.1172/jci.insight.155432