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...

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Autores principales: Yoon Seok Choi, Jung Eun Lee, Seung Joo Nam, Jung Tak Park, Hyon-Suk Kim, Kyu Hun Choi, Beom Seok Kim, Eui-Cheol Shin
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:3413065f77504c579c760f8b8868175c2021-11-18T07:47:31ZTwo distinct functional patterns of hepatitis C Virus (HCV)-specific T cell responses in seronegative, aviremic patients.1932-620310.1371/journal.pone.0062319https://doaj.org/article/3413065f77504c579c760f8b8868175c2013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23638039/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203In 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.Yoon Seok ChoiJung Eun LeeSeung Joo NamJung Tak ParkHyon-Suk KimKyu Hun ChoiBeom Seok KimEui-Cheol ShinPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 4, p e62319 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
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.
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.
format article
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
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)
publishDate 2013
url https://doaj.org/article/3413065f77504c579c760f8b8868175c
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