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Expression of programmed cell death protein 1 and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood CD4+CD8+ double positive T cells in patients with chronic hepatitis C virus infection and in subjects who spontaneously cleared the virus

Chronic hepatitis C virus (HCV) infection is characterized by increased proportion of CD4+CD8+ double positive (DP) T cells, but their role in this infection is unclear. In chronic hepatitis C, immune responses to HCV become functionally exhausted, which manifests itself by increased expression of p...

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Autores principales: Caraballo Cortés, Kamila, Osuch, Sylwia, Perlejewski, Karol, Pawełczyk, Agnieszka, Kaźmierczak, Justyna, Janiak, Maciej, Jabłońska, Joanna, Nazzal, Khalil, Stelmaszczyk‐Emmel, Anna, Berak, Hanna, Bukowska‐Ośko, Iwona, Paciorek, Marcin, Laskus, Tomasz, Radkowski, Marek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850126/
https://www.ncbi.nlm.nih.gov/pubmed/30972915
http://dx.doi.org/10.1111/jvh.13108
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author Caraballo Cortés, Kamila
Osuch, Sylwia
Perlejewski, Karol
Pawełczyk, Agnieszka
Kaźmierczak, Justyna
Janiak, Maciej
Jabłońska, Joanna
Nazzal, Khalil
Stelmaszczyk‐Emmel, Anna
Berak, Hanna
Bukowska‐Ośko, Iwona
Paciorek, Marcin
Laskus, Tomasz
Radkowski, Marek
author_facet Caraballo Cortés, Kamila
Osuch, Sylwia
Perlejewski, Karol
Pawełczyk, Agnieszka
Kaźmierczak, Justyna
Janiak, Maciej
Jabłońska, Joanna
Nazzal, Khalil
Stelmaszczyk‐Emmel, Anna
Berak, Hanna
Bukowska‐Ośko, Iwona
Paciorek, Marcin
Laskus, Tomasz
Radkowski, Marek
author_sort Caraballo Cortés, Kamila
collection PubMed
description Chronic hepatitis C virus (HCV) infection is characterized by increased proportion of CD4+CD8+ double positive (DP) T cells, but their role in this infection is unclear. In chronic hepatitis C, immune responses to HCV become functionally exhausted, which manifests itself by increased expression of programmed cell death protein 1 (PD‐1) and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 (Tim‐3) on T cells. The aim of our study was to determine PD‐1 and Tim‐3 phenotype of DP T cells in subjects with naturally resolved and chronic HCV infection. Peripheral blood mononuclear cells from 16 patients with chronic infection and 14 subjects who cleared HCV in the past were stained with anti‐CD3, anti‐CD4, anti‐CD8, anti‐PD‐1 and anti‐Tim‐3 antibodies and, in 12 HLA‐A*02‐positive subjects, MHC class I pentamer with HCV NS3(1406) epitope. In chronic and past HCV infection, proportions of total DP T cells and PD‐1+ DP T cells were similar but significantly higher than in healthy controls. DP T cells were more likely to be PD‐1+ than either CD4+ or CD8+ single positive (SP) T cells. HCV‐specific cells were present in higher proportions among DP T cells than among CD8+ SP T cells in both patient groups. Furthermore, while the majority of HCV‐specific DP T cells were PD‐1+, the proportion of HCV‐specific CD8+ T cells which were PD‐1+ was 4.9 and 1.9 times lower (chronic and past infection, respectively). PD‐1 and Tim‐3 were predominantly expressed on CD4(high)CD8(low) and CD4(low)CD8(high) cells, respectively, and co‐expression of both markers was uncommon.
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spelling pubmed-68501262019-11-15 Expression of programmed cell death protein 1 and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood CD4+CD8+ double positive T cells in patients with chronic hepatitis C virus infection and in subjects who spontaneously cleared the virus Caraballo Cortés, Kamila Osuch, Sylwia Perlejewski, Karol Pawełczyk, Agnieszka Kaźmierczak, Justyna Janiak, Maciej Jabłońska, Joanna Nazzal, Khalil Stelmaszczyk‐Emmel, Anna Berak, Hanna Bukowska‐Ośko, Iwona Paciorek, Marcin Laskus, Tomasz Radkowski, Marek J Viral Hepat Original Articles Chronic hepatitis C virus (HCV) infection is characterized by increased proportion of CD4+CD8+ double positive (DP) T cells, but their role in this infection is unclear. In chronic hepatitis C, immune responses to HCV become functionally exhausted, which manifests itself by increased expression of programmed cell death protein 1 (PD‐1) and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 (Tim‐3) on T cells. The aim of our study was to determine PD‐1 and Tim‐3 phenotype of DP T cells in subjects with naturally resolved and chronic HCV infection. Peripheral blood mononuclear cells from 16 patients with chronic infection and 14 subjects who cleared HCV in the past were stained with anti‐CD3, anti‐CD4, anti‐CD8, anti‐PD‐1 and anti‐Tim‐3 antibodies and, in 12 HLA‐A*02‐positive subjects, MHC class I pentamer with HCV NS3(1406) epitope. In chronic and past HCV infection, proportions of total DP T cells and PD‐1+ DP T cells were similar but significantly higher than in healthy controls. DP T cells were more likely to be PD‐1+ than either CD4+ or CD8+ single positive (SP) T cells. HCV‐specific cells were present in higher proportions among DP T cells than among CD8+ SP T cells in both patient groups. Furthermore, while the majority of HCV‐specific DP T cells were PD‐1+, the proportion of HCV‐specific CD8+ T cells which were PD‐1+ was 4.9 and 1.9 times lower (chronic and past infection, respectively). PD‐1 and Tim‐3 were predominantly expressed on CD4(high)CD8(low) and CD4(low)CD8(high) cells, respectively, and co‐expression of both markers was uncommon. John Wiley and Sons Inc. 2019-04-29 2019-08 /pmc/articles/PMC6850126/ /pubmed/30972915 http://dx.doi.org/10.1111/jvh.13108 Text en © 2019 The Authors. Journal of Viral Hepatitis Published by John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Caraballo Cortés, Kamila
Osuch, Sylwia
Perlejewski, Karol
Pawełczyk, Agnieszka
Kaźmierczak, Justyna
Janiak, Maciej
Jabłońska, Joanna
Nazzal, Khalil
Stelmaszczyk‐Emmel, Anna
Berak, Hanna
Bukowska‐Ośko, Iwona
Paciorek, Marcin
Laskus, Tomasz
Radkowski, Marek
Expression of programmed cell death protein 1 and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood CD4+CD8+ double positive T cells in patients with chronic hepatitis C virus infection and in subjects who spontaneously cleared the virus
title Expression of programmed cell death protein 1 and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood CD4+CD8+ double positive T cells in patients with chronic hepatitis C virus infection and in subjects who spontaneously cleared the virus
title_full Expression of programmed cell death protein 1 and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood CD4+CD8+ double positive T cells in patients with chronic hepatitis C virus infection and in subjects who spontaneously cleared the virus
title_fullStr Expression of programmed cell death protein 1 and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood CD4+CD8+ double positive T cells in patients with chronic hepatitis C virus infection and in subjects who spontaneously cleared the virus
title_full_unstemmed Expression of programmed cell death protein 1 and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood CD4+CD8+ double positive T cells in patients with chronic hepatitis C virus infection and in subjects who spontaneously cleared the virus
title_short Expression of programmed cell death protein 1 and T‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood CD4+CD8+ double positive T cells in patients with chronic hepatitis C virus infection and in subjects who spontaneously cleared the virus
title_sort expression of programmed cell death protein 1 and t‐cell immunoglobulin‐ and mucin‐domain‐containing molecule‐3 on peripheral blood cd4+cd8+ double positive t cells in patients with chronic hepatitis c virus infection and in subjects who spontaneously cleared the virus
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850126/
https://www.ncbi.nlm.nih.gov/pubmed/30972915
http://dx.doi.org/10.1111/jvh.13108
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