Efficacy of extracorporeal immunoadsorption therapy for removal of HBsAg

Abstract The purpose of chronic hepatitis B (CHB) treatment is functional cure (FC). It refers to the removal of hepatitis B surface antigen (HBsAg) from the serum. However, this outcome is rare with current treatments due to the presence of integrated hepatitis B virus (HBV) DNA and intrahepatic co...

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Main Authors: Meng Wang, Qi Zhou, Huan Wu, Yefu Wang
Format: Article
Language:English
Published: BMC 2025-07-01
Series:BMC Gastroenterology
Subjects:
Online Access:https://doi.org/10.1186/s12876-025-04062-z
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author Meng Wang
Qi Zhou
Huan Wu
Yefu Wang
author_facet Meng Wang
Qi Zhou
Huan Wu
Yefu Wang
author_sort Meng Wang
collection DOAJ
description Abstract The purpose of chronic hepatitis B (CHB) treatment is functional cure (FC). It refers to the removal of hepatitis B surface antigen (HBsAg) from the serum. However, this outcome is rare with current treatments due to the presence of integrated hepatitis B virus (HBV) DNA and intrahepatic covalently closed circular DNA (cccDNA). This study investigates the efficacy of removal of HBsAg using immunoadsorption. An immunosorbent was prepared by coupling anti-HBsAg monoclonal antibodies to agarose beads, selected from six candidates based on adsorption efficiency. Then the adsorbents were characterized by scanning electron microscopy (SEM) and energy dispersive spectrometer (EDS). V79 lung fibroblasts were used to determine the cytotoxicity of the immunosorbent through in vitro viability assays. The results indicated that the immunosorbent was non-cytotoxic. Static and dynamic adsorption studies in vitro demonstrated efficient HBsAg removal. To validate therapeutic potential, an extracorporeal circulation system equipped with the immunosorbent (10 ml sorbent column) was tested in rabbits injected with HBsAg-positive rabbit serum. This system selectively reduced serum HBsAg levels by 76.38 ± 1.37% and HBV DNA by 66.20 ± 0.85%. Given the absence of existing therapies capable of reducing HBsAg directly, our findings suggest that combining immunoadsorption with HBV drugs may serve as a novel therapeutic strategy—or at least provide a valuable adjunct—to advance functional cure efforts in CHB. Further clinical validation is warranted.
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spelling doaj-art-9b56353cd7d743f2ab72e24a515b1cc82025-08-20T04:01:35ZengBMCBMC Gastroenterology1471-230X2025-07-0125111110.1186/s12876-025-04062-zEfficacy of extracorporeal immunoadsorption therapy for removal of HBsAgMeng Wang0Qi Zhou1Huan Wu2Yefu Wang3State Key Laboratory of Virology, College of Life Sciences, Wuhan UniversityState Key Laboratory of Virology, College of Life Sciences, Wuhan UniversityState Key Laboratory of Virology, College of Life Sciences, Wuhan UniversityState Key Laboratory of Virology, College of Life Sciences, Wuhan UniversityAbstract The purpose of chronic hepatitis B (CHB) treatment is functional cure (FC). It refers to the removal of hepatitis B surface antigen (HBsAg) from the serum. However, this outcome is rare with current treatments due to the presence of integrated hepatitis B virus (HBV) DNA and intrahepatic covalently closed circular DNA (cccDNA). This study investigates the efficacy of removal of HBsAg using immunoadsorption. An immunosorbent was prepared by coupling anti-HBsAg monoclonal antibodies to agarose beads, selected from six candidates based on adsorption efficiency. Then the adsorbents were characterized by scanning electron microscopy (SEM) and energy dispersive spectrometer (EDS). V79 lung fibroblasts were used to determine the cytotoxicity of the immunosorbent through in vitro viability assays. The results indicated that the immunosorbent was non-cytotoxic. Static and dynamic adsorption studies in vitro demonstrated efficient HBsAg removal. To validate therapeutic potential, an extracorporeal circulation system equipped with the immunosorbent (10 ml sorbent column) was tested in rabbits injected with HBsAg-positive rabbit serum. This system selectively reduced serum HBsAg levels by 76.38 ± 1.37% and HBV DNA by 66.20 ± 0.85%. Given the absence of existing therapies capable of reducing HBsAg directly, our findings suggest that combining immunoadsorption with HBV drugs may serve as a novel therapeutic strategy—or at least provide a valuable adjunct—to advance functional cure efforts in CHB. Further clinical validation is warranted.https://doi.org/10.1186/s12876-025-04062-zHBVHBsAgMonoclonal antibodyAgarose beadsExtracorporeal immunoadsorptionRabbits
spellingShingle Meng Wang
Qi Zhou
Huan Wu
Yefu Wang
Efficacy of extracorporeal immunoadsorption therapy for removal of HBsAg
BMC Gastroenterology
HBV
HBsAg
Monoclonal antibody
Agarose beads
Extracorporeal immunoadsorption
Rabbits
title Efficacy of extracorporeal immunoadsorption therapy for removal of HBsAg
title_full Efficacy of extracorporeal immunoadsorption therapy for removal of HBsAg
title_fullStr Efficacy of extracorporeal immunoadsorption therapy for removal of HBsAg
title_full_unstemmed Efficacy of extracorporeal immunoadsorption therapy for removal of HBsAg
title_short Efficacy of extracorporeal immunoadsorption therapy for removal of HBsAg
title_sort efficacy of extracorporeal immunoadsorption therapy for removal of hbsag
topic HBV
HBsAg
Monoclonal antibody
Agarose beads
Extracorporeal immunoadsorption
Rabbits
url https://doi.org/10.1186/s12876-025-04062-z
work_keys_str_mv AT mengwang efficacyofextracorporealimmunoadsorptiontherapyforremovalofhbsag
AT qizhou efficacyofextracorporealimmunoadsorptiontherapyforremovalofhbsag
AT huanwu efficacyofextracorporealimmunoadsorptiontherapyforremovalofhbsag
AT yefuwang efficacyofextracorporealimmunoadsorptiontherapyforremovalofhbsag