Two distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients.
In hepatitis C Virus (HCV) high-risk groups, HCV-specific T cell responses have been detected in seronegative, aviremic persons who have no evidence of HCV infection. Herein, we investigated functional profiles of HCV-specific T-cell responses in seronegative, aviremic patients of a HCV high-risk gr...
Main Authors: | , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2013-01-01
|
Series: | PLoS ONE |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23638039/pdf/?tool=EBI |
id |
doaj-3413065f77504c579c760f8b8868175c |
---|---|
record_format |
Article |
spelling |
doaj-3413065f77504c579c760f8b8868175c2021-03-03T23:25:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0184e6231910.1371/journal.pone.0062319Two distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients.Yoon Seok ChoiJung Eun LeeSeung Joo NamJung Tak ParkHyon-Suk KimKyu Hun ChoiBeom Seok KimEui-Cheol ShinIn hepatitis C Virus (HCV) high-risk groups, HCV-specific T cell responses have been detected in seronegative, aviremic persons who have no evidence of HCV infection. Herein, we investigated functional profiles of HCV-specific T-cell responses in seronegative, aviremic patients of a HCV high-risk group. Seventy seven hemodialysis patients with chronic renal disease were analyzed by IFN-γ ELISpot assays, and eight of 71 (11.3%) seronegative, aviremic patients displayed HCV-specific T-cell responses. Their HCV-specific memory T cells were characterized by assessing cytokine polyfunctionality, known to provide antiviral protection. By intracellular staining of IFN-γ, TNF-α, IL-2 and MIP-1β, we identified two distinct populations in the seronegative, aviremic patients: polyfunctional responders and TNF-α-predominant responders. In further analysis, occult HCV infection was excluded as a cause of the HCV-specific T cell response via secondary nested RT-PCR of HCV RNA in peripheral blood mononuclear cell samples. HCV-specific T cells targeted multiple epitopes including non-structural proteins in a single patient, implying that their T cells might have been primed by HCV proteins synthesized within the host. We conclude that HCV-specific memory T cells of seronegative, aviremic patients arise from authentic HCV replication in the host, but not from current occult HCV infection. By functional pattern of HCV-specific T cells, there are two distinct populations in these patients: polyfunctional responders and TNF-α-predominant responders.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23638039/pdf/?tool=EBI |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yoon Seok Choi Jung Eun Lee Seung Joo Nam Jung Tak Park Hyon-Suk Kim Kyu Hun Choi Beom Seok Kim Eui-Cheol Shin |
spellingShingle |
Yoon Seok Choi Jung Eun Lee Seung Joo Nam Jung Tak Park Hyon-Suk Kim Kyu Hun Choi Beom Seok Kim Eui-Cheol Shin Two distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients. PLoS ONE |
author_facet |
Yoon Seok Choi Jung Eun Lee Seung Joo Nam Jung Tak Park Hyon-Suk Kim Kyu Hun Choi Beom Seok Kim Eui-Cheol Shin |
author_sort |
Yoon Seok Choi |
title |
Two distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients. |
title_short |
Two distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients. |
title_full |
Two distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients. |
title_fullStr |
Two distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients. |
title_full_unstemmed |
Two distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients. |
title_sort |
two distinct functional patterns of hepatitis c virus (hcv)-specific t cell responses in seronegative, aviremic patients. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2013-01-01 |
description |
In hepatitis C Virus (HCV) high-risk groups, HCV-specific T cell responses have been detected in seronegative, aviremic persons who have no evidence of HCV infection. Herein, we investigated functional profiles of HCV-specific T-cell responses in seronegative, aviremic patients of a HCV high-risk group. Seventy seven hemodialysis patients with chronic renal disease were analyzed by IFN-γ ELISpot assays, and eight of 71 (11.3%) seronegative, aviremic patients displayed HCV-specific T-cell responses. Their HCV-specific memory T cells were characterized by assessing cytokine polyfunctionality, known to provide antiviral protection. By intracellular staining of IFN-γ, TNF-α, IL-2 and MIP-1β, we identified two distinct populations in the seronegative, aviremic patients: polyfunctional responders and TNF-α-predominant responders. In further analysis, occult HCV infection was excluded as a cause of the HCV-specific T cell response via secondary nested RT-PCR of HCV RNA in peripheral blood mononuclear cell samples. HCV-specific T cells targeted multiple epitopes including non-structural proteins in a single patient, implying that their T cells might have been primed by HCV proteins synthesized within the host. We conclude that HCV-specific memory T cells of seronegative, aviremic patients arise from authentic HCV replication in the host, but not from current occult HCV infection. By functional pattern of HCV-specific T cells, there are two distinct populations in these patients: polyfunctional responders and TNF-α-predominant responders. |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23638039/pdf/?tool=EBI |
work_keys_str_mv |
AT yoonseokchoi twodistinctfunctionalpatternsofhepatitiscvirushcvspecifictcellresponsesinseronegativeaviremicpatients AT jungeunlee twodistinctfunctionalpatternsofhepatitiscvirushcvspecifictcellresponsesinseronegativeaviremicpatients AT seungjoonam twodistinctfunctionalpatternsofhepatitiscvirushcvspecifictcellresponsesinseronegativeaviremicpatients AT jungtakpark twodistinctfunctionalpatternsofhepatitiscvirushcvspecifictcellresponsesinseronegativeaviremicpatients AT hyonsukkim twodistinctfunctionalpatternsofhepatitiscvirushcvspecifictcellresponsesinseronegativeaviremicpatients AT kyuhunchoi twodistinctfunctionalpatternsofhepatitiscvirushcvspecifictcellresponsesinseronegativeaviremicpatients AT beomseokkim twodistinctfunctionalpatternsofhepatitiscvirushcvspecifictcellresponsesinseronegativeaviremicpatients AT euicheolshin twodistinctfunctionalpatternsofhepatitiscvirushcvspecifictcellresponsesinseronegativeaviremicpatients |
_version_ |
1714811506562957312 |