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Preserved Function of Circulating Invariant Natural Killer T Cells in Patients With Chronic Hepatitis B Virus Infection

To date, the role of invariant natural killer T (iNKT) cells in chronic hepatitis B virus (HBV) infection is not fully understood. In previous reports, iNKT cells were identified by indirect methods. However, discrepancies regarding the prevalence and function of iNKT cells during HBV infection were...

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Autores principales: Zhu, Haoxiang, Zhang, Yongmei, Liu, Hongyan, Zhang, Yijun, Kang, Yaoyue, Mao, Richeng, Yang, Feifei, Zhou, Dapeng, Zhang, Jiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616535/
https://www.ncbi.nlm.nih.gov/pubmed/26091463
http://dx.doi.org/10.1097/MD.0000000000000961
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author Zhu, Haoxiang
Zhang, Yongmei
Liu, Hongyan
Zhang, Yijun
Kang, Yaoyue
Mao, Richeng
Yang, Feifei
Zhou, Dapeng
Zhang, Jiming
author_facet Zhu, Haoxiang
Zhang, Yongmei
Liu, Hongyan
Zhang, Yijun
Kang, Yaoyue
Mao, Richeng
Yang, Feifei
Zhou, Dapeng
Zhang, Jiming
author_sort Zhu, Haoxiang
collection PubMed
description To date, the role of invariant natural killer T (iNKT) cells in chronic hepatitis B virus (HBV) infection is not fully understood. In previous reports, iNKT cells were identified by indirect methods. However, discrepancies regarding the prevalence and function of iNKT cells during HBV infection were observed. In this study, we have devised a direct, highly specific CD1d tetramer-based methodology to test whether patients with HBV infection have associated iNKT-cell defects. In our study, a total of 93 chronic HBV-infected patients and 30 healthy individuals (as control) were enrolled. The prevalence of iNKT cells, their cytokine producing capacity, and in vitro expansion were determined by flow cytometric analysis with CD1d tetramer staining. Our observation demonstrated that there was no significant difference in circulating CD1d-tetramer positive iNKT cell numbers between HBV-infected patients and healthy controls. The capacity of iNKT cells to produce IFN-γ or IL-4 as well as their in vitro expansion was also comparable between these 2 groups. However, among chronic HBV-infected patients, a decrease in iNKT cell-number was observed in chronic hepatitis B (CHB) and cirrhosis patients in comparison to that in immune tolerant (IT) patients. These results indicated that patients with chronic HBV infection may have normal prevalence and preserved function of circulating iNKT cells. And antiviral therapy with nucleot(s)ide analogue does not alter the frequency and function of circulating iNKT cells in chronic Hepatitis B patients.
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spelling pubmed-46165352015-10-27 Preserved Function of Circulating Invariant Natural Killer T Cells in Patients With Chronic Hepatitis B Virus Infection Zhu, Haoxiang Zhang, Yongmei Liu, Hongyan Zhang, Yijun Kang, Yaoyue Mao, Richeng Yang, Feifei Zhou, Dapeng Zhang, Jiming Medicine (Baltimore) 4500 To date, the role of invariant natural killer T (iNKT) cells in chronic hepatitis B virus (HBV) infection is not fully understood. In previous reports, iNKT cells were identified by indirect methods. However, discrepancies regarding the prevalence and function of iNKT cells during HBV infection were observed. In this study, we have devised a direct, highly specific CD1d tetramer-based methodology to test whether patients with HBV infection have associated iNKT-cell defects. In our study, a total of 93 chronic HBV-infected patients and 30 healthy individuals (as control) were enrolled. The prevalence of iNKT cells, their cytokine producing capacity, and in vitro expansion were determined by flow cytometric analysis with CD1d tetramer staining. Our observation demonstrated that there was no significant difference in circulating CD1d-tetramer positive iNKT cell numbers between HBV-infected patients and healthy controls. The capacity of iNKT cells to produce IFN-γ or IL-4 as well as their in vitro expansion was also comparable between these 2 groups. However, among chronic HBV-infected patients, a decrease in iNKT cell-number was observed in chronic hepatitis B (CHB) and cirrhosis patients in comparison to that in immune tolerant (IT) patients. These results indicated that patients with chronic HBV infection may have normal prevalence and preserved function of circulating iNKT cells. And antiviral therapy with nucleot(s)ide analogue does not alter the frequency and function of circulating iNKT cells in chronic Hepatitis B patients. Wolters Kluwer Health 2015-06-19 /pmc/articles/PMC4616535/ /pubmed/26091463 http://dx.doi.org/10.1097/MD.0000000000000961 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the Creative Commons Attribution-NonCommercial License, where it is permissible to download, share and reproduce the work in any medium, provided it is properly cited. The work cannot be used commercially. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 4500
Zhu, Haoxiang
Zhang, Yongmei
Liu, Hongyan
Zhang, Yijun
Kang, Yaoyue
Mao, Richeng
Yang, Feifei
Zhou, Dapeng
Zhang, Jiming
Preserved Function of Circulating Invariant Natural Killer T Cells in Patients With Chronic Hepatitis B Virus Infection
title Preserved Function of Circulating Invariant Natural Killer T Cells in Patients With Chronic Hepatitis B Virus Infection
title_full Preserved Function of Circulating Invariant Natural Killer T Cells in Patients With Chronic Hepatitis B Virus Infection
title_fullStr Preserved Function of Circulating Invariant Natural Killer T Cells in Patients With Chronic Hepatitis B Virus Infection
title_full_unstemmed Preserved Function of Circulating Invariant Natural Killer T Cells in Patients With Chronic Hepatitis B Virus Infection
title_short Preserved Function of Circulating Invariant Natural Killer T Cells in Patients With Chronic Hepatitis B Virus Infection
title_sort preserved function of circulating invariant natural killer t cells in patients with chronic hepatitis b virus infection
topic 4500
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4616535/
https://www.ncbi.nlm.nih.gov/pubmed/26091463
http://dx.doi.org/10.1097/MD.0000000000000961
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