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Profiling of Peripheral TRBV and CD4+CD25+ Treg in CHB Patients with HBeAg SC during TDF Treatment

BACKGROUND: It is lacking that markers could predict the prognosis of chronic hepatitis B (CHB) subjects during antiviral treatment, and the related cellular immune mechanism is not fully evaluated. AIM: To explore the comprehensive profile of T cell receptor β-chain (TRBV) and CD4+CD25+ regulatory...

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Autores principales: Yang, Jiezuan, Lu, Haifeng, Chen, Baikun, Jiang, Lili, Zhang, Hua, Ye, Ping, Jin, Linfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845053/
https://www.ncbi.nlm.nih.gov/pubmed/36660247
http://dx.doi.org/10.1155/2023/1914036
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author Yang, Jiezuan
Lu, Haifeng
Chen, Baikun
Jiang, Lili
Zhang, Hua
Ye, Ping
Jin, Linfeng
author_facet Yang, Jiezuan
Lu, Haifeng
Chen, Baikun
Jiang, Lili
Zhang, Hua
Ye, Ping
Jin, Linfeng
author_sort Yang, Jiezuan
collection PubMed
description BACKGROUND: It is lacking that markers could predict the prognosis of chronic hepatitis B (CHB) subjects during antiviral treatment, and the related cellular immune mechanism is not fully evaluated. AIM: To explore the comprehensive profile of T cell receptor β-chain (TRBV) and CD4+CD25+ regulatory T cell (Treg) in peripheral blood of CHB patients with HBeAg seroconverting (SC) during tenofovir disoproxil fumarate (TDF) treatment. METHODS: The frequency of CD4+CD25high+ Treg and number of skewed TRBV in 20 HBeAg positive patients were determined at baseline and following every 12 weeks during 96-week TDF treatment. The relationship among serum alanine aminotransferase (ALT) level, HBV DNA load, Treg frequency, and the number of skewed TRBV, respectively, was analyzed for CHB patients. Receiver operative characteristic curve was applied to analyze their diagnostic value for HBeAg SC. RESULTS: The number of skewed TRBV at week 48, Treg frequency at week 72, and ALT level at baseline could predict the HBeAg SC or non-SC in CHB patients during 96-week TDF treatment. Moreover, the positive correlation between ALT or HBV DNA and Treg levels or skewed TRBVs was significant in the SC group, but not in non-SC. CONCLUSIONS: The predictive cutoff value of ALT for HBeAg SC was 178 U/L at baseline. Moreover, the ALT, Treg, and TRBV families would be associated with the prognosis and pathogenesis of CHB patients during TDF treatment.
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spelling pubmed-98450532023-01-18 Profiling of Peripheral TRBV and CD4+CD25+ Treg in CHB Patients with HBeAg SC during TDF Treatment Yang, Jiezuan Lu, Haifeng Chen, Baikun Jiang, Lili Zhang, Hua Ye, Ping Jin, Linfeng J Immunol Res Research Article BACKGROUND: It is lacking that markers could predict the prognosis of chronic hepatitis B (CHB) subjects during antiviral treatment, and the related cellular immune mechanism is not fully evaluated. AIM: To explore the comprehensive profile of T cell receptor β-chain (TRBV) and CD4+CD25+ regulatory T cell (Treg) in peripheral blood of CHB patients with HBeAg seroconverting (SC) during tenofovir disoproxil fumarate (TDF) treatment. METHODS: The frequency of CD4+CD25high+ Treg and number of skewed TRBV in 20 HBeAg positive patients were determined at baseline and following every 12 weeks during 96-week TDF treatment. The relationship among serum alanine aminotransferase (ALT) level, HBV DNA load, Treg frequency, and the number of skewed TRBV, respectively, was analyzed for CHB patients. Receiver operative characteristic curve was applied to analyze their diagnostic value for HBeAg SC. RESULTS: The number of skewed TRBV at week 48, Treg frequency at week 72, and ALT level at baseline could predict the HBeAg SC or non-SC in CHB patients during 96-week TDF treatment. Moreover, the positive correlation between ALT or HBV DNA and Treg levels or skewed TRBVs was significant in the SC group, but not in non-SC. CONCLUSIONS: The predictive cutoff value of ALT for HBeAg SC was 178 U/L at baseline. Moreover, the ALT, Treg, and TRBV families would be associated with the prognosis and pathogenesis of CHB patients during TDF treatment. Hindawi 2023-01-10 /pmc/articles/PMC9845053/ /pubmed/36660247 http://dx.doi.org/10.1155/2023/1914036 Text en Copyright © 2023 Jiezuan Yang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yang, Jiezuan
Lu, Haifeng
Chen, Baikun
Jiang, Lili
Zhang, Hua
Ye, Ping
Jin, Linfeng
Profiling of Peripheral TRBV and CD4+CD25+ Treg in CHB Patients with HBeAg SC during TDF Treatment
title Profiling of Peripheral TRBV and CD4+CD25+ Treg in CHB Patients with HBeAg SC during TDF Treatment
title_full Profiling of Peripheral TRBV and CD4+CD25+ Treg in CHB Patients with HBeAg SC during TDF Treatment
title_fullStr Profiling of Peripheral TRBV and CD4+CD25+ Treg in CHB Patients with HBeAg SC during TDF Treatment
title_full_unstemmed Profiling of Peripheral TRBV and CD4+CD25+ Treg in CHB Patients with HBeAg SC during TDF Treatment
title_short Profiling of Peripheral TRBV and CD4+CD25+ Treg in CHB Patients with HBeAg SC during TDF Treatment
title_sort profiling of peripheral trbv and cd4+cd25+ treg in chb patients with hbeag sc during tdf treatment
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845053/
https://www.ncbi.nlm.nih.gov/pubmed/36660247
http://dx.doi.org/10.1155/2023/1914036
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