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Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C
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)...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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American Society for Clinical Investigation
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855829/ https://www.ncbi.nlm.nih.gov/pubmed/34905514 http://dx.doi.org/10.1172/jci.insight.155432 |
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author | Senff, Tina Menne, Christopher Cosmovici, Christine Lewis-Ximenez, Lia Laura Aneja, Jasneet Broering, Ruth Kim, Arthur Y. Westendorf, Astrid M. Dittmer, Ulf Scherbaum, Norbert Lauer, Georg M. Timm, Jörg |
author_facet | Senff, Tina Menne, Christopher Cosmovici, Christine Lewis-Ximenez, Lia Laura Aneja, Jasneet Broering, Ruth Kim, Arthur Y. Westendorf, Astrid M. Dittmer, Ulf Scherbaum, Norbert Lauer, Georg M. Timm, Jörg |
author_sort | Senff, Tina |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-8855829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society for Clinical Investigation |
record_format | MEDLINE/PubMed |
spelling | pubmed-88558292022-02-22 Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C Senff, Tina Menne, Christopher Cosmovici, Christine Lewis-Ximenez, Lia Laura Aneja, Jasneet Broering, Ruth Kim, Arthur Y. Westendorf, Astrid M. Dittmer, Ulf Scherbaum, Norbert Lauer, Georg M. Timm, Jörg JCI Insight Research Article 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. American Society for Clinical Investigation 2022-01-25 /pmc/articles/PMC8855829/ /pubmed/34905514 http://dx.doi.org/10.1172/jci.insight.155432 Text en © 2022 Senff et al. https://creativecommons.org/licenses/by/4.0/This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Article Senff, Tina Menne, Christopher Cosmovici, Christine Lewis-Ximenez, Lia Laura Aneja, Jasneet Broering, Ruth Kim, Arthur Y. Westendorf, Astrid M. Dittmer, Ulf Scherbaum, Norbert Lauer, Georg M. Timm, Jörg Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C |
title | Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C |
title_full | Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C |
title_fullStr | Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C |
title_full_unstemmed | Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C |
title_short | Peripheral blood iNKT cell activation correlates with liver damage during acute hepatitis C |
title_sort | peripheral blood inkt cell activation correlates with liver damage during acute hepatitis c |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855829/ https://www.ncbi.nlm.nih.gov/pubmed/34905514 http://dx.doi.org/10.1172/jci.insight.155432 |
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