Bibliographic Details
Title: |
A hepatitis B virus-derived peptide combined with HBsAg exerts an anti-HBV effect in an HBV transgenic mouse model as a therapeutic vaccine |
Authors: |
Yu-Min Choi, Dong Hyun Kim, Junghwa Jang, Bum-Joon Kim |
Source: |
Frontiers in Immunology, Vol 14 (2023) |
Publisher Information: |
Frontiers Media S.A., 2023. |
Publication Year: |
2023 |
Collection: |
LCC:Immunologic diseases. Allergy |
Subject Terms: |
hepatitis B virus (HBV), therapeutic vaccination, adjuvant, type 1 interferon (IFN-I), (HBV)-derived peptide, Poly6, Immunologic diseases. Allergy, RC581-607 |
More Details: |
IntroductionFor complete or functional cure of hepatitis B virus (HBV) infection, application of immunotherapy is now being attempted. Recently, we reported that a 6-mer hepatitis B virus (HBV)-derived peptide, Poly6, exerts a strong anticancer effect in tumor-implanted mice through inducible nitric oxide synthase (iNOS)-producing DCs (Tip-DCs) in a type 1 interferon (IFN-I)-dependent manner, suggesting its potential as a vaccine adjuvant.MethodsIn this study, we explored the potential of Poly6 in combination with HBsAg as a therapeutic vaccine against hepatitis B virus infection. We investigated the immunotherapeutic potential of Poly6 combined with HBsAg vaccination against hepatitis B virus infection in C57BL/6 mice or an HBV transgenic mouse model.ResultsIn C57BL/6 mice, Poly6 enhanced DC maturation and DC migration capacity in an IFN-I-dependent manner. Moreover, the addition of Poly6 to alum in combination with HBsAg also led to enhanced HBsAg-specific cell-mediated immune (CMI) responses, suggesting its potential as an adjuvant of HBsAg-based vaccines. In HBV transgenic mice, vaccination with Poly6 combined with HBsAg exerted a strong anti-HBV effect via induction of HBV-specific humoral and cell-mediated immune responses. In addition, it also induced HBV-specific effector memory T cells (TEM).DiscussionOur data indicated that vaccination with Poly6 in combination with HBsAg exerts an anti-HBV effect in HBV transgenic mice, which is mainly mediated by HBV-specific CMI and humoral immune responses via IFN-I-dependent DC activation, suggesting the feasibility of Poly6 as an adjuvant for an HBV therapeutic vaccine. |
Document Type: |
article |
File Description: |
electronic resource |
Language: |
English |
ISSN: |
1664-3224 |
Relation: |
https://www.frontiersin.org/articles/10.3389/fimmu.2023.1155637/full; https://doaj.org/toc/1664-3224 |
DOI: |
10.3389/fimmu.2023.1155637 |
Access URL: |
https://doaj.org/article/90c20610facd42d78d3066b0fddbc4d9 |
Accession Number: |
edsdoj.90c20610facd42d78d3066b0fddbc4d9 |
Database: |
Directory of Open Access Journals |