题名 | Analysis of epitope-based vaccine candidates against the E antigen of the hepatitis B virus based on the B genotype sequence: An in silico and in vitro approach |
作者 | |
发表日期 | 2018-07 |
发表期刊 | CELLULAR IMMUNOLOGY 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | Bioinformatics Epitope Hepatitis B virus E antigen Therapeutic vaccine |
其他关键词 | T-CELL-EPITOPES ; STRUCTURE PREDICTION ; IMMUNE-RESPONSE ; NEURAL-NETWORKS ; HBV INFECTION ; PEP-FOLD ; PEPTIDES ; HBEAG ; PROTEINS ; CURE |
摘要 | Chronic hepatitis B virus infection is a worldwide health problem with no current effective strategy to achieve a cure. The Hepatitis B virus (HBV) E antigen (HBeAg) has a negative effect on the immune system and a therapeutic vaccine is a promising strategy in order to treat chronic virus infection. In this study, we analyzed and identified the MHC-I, MHC-II and B cell epitopes of the HBeAg based on a B genotype sequence of HBV using a bioinformatic approach and in vitro experiments. The computational approach provided us with four epitopes (LLWFHISCL, YLVSFGVWI, MQLFHLCLI, TVLEYLVSF) of the specific MHC-I allele HLA-A0201 that conformed to all criteria. Molecular docking and a peptide binding assay showed that epitope TVLEYLVSF had the lowest binding energy and epitope LLWFHISCL had the highest binding affinity to the HLA-A0201 molecule. An interferon.enzyme-linked immunospot assay and cytotoxicity assay revealed that epitope LLWFHISCL had the highest ability to induce and stimulate T cells. Furthermore, we determined four core peptides of MHC-II epitopes and a region of the B cell epitope. The epitopes and region identified in this research may be helpful in designing epitope-based vaccines and boosting the mechanism research of HBeAg and its effect on the immune system. |
资助项目 | Natural Science Foundation of Zhejiang ProvinceNatural Science Foundation of Zhejiang Province [Y2110768, LY12H03003]; Technology Bureau of Wenzhou [2014Y0136] |
出版者 | ACADEMIC PRESS INC ELSEVIER SCIENCE |
出版地 | SAN DIEGO |
ISSN | 0008-8749 |
EISSN | 1090-2163 |
卷号 | 329页码:56-65 |
DOI | 10.1016/j.cellimm.2018.04.015 |
页数 | 10 |
WOS类目 | Cell Biology ; Immunology |
WOS研究方向 | Cell Biology ; Immunology |
WOS记录号 | WOS:000434286200008 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 29724463 |
SCOPUSEID | 2-s2.0-85046373580 |
通讯作者地址 | [Wu, Jinming]Department of Gastroenterology,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325000,China |
Scopus学科分类 | Immunology |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/13316 |
专题 | 附属第一医院 其他_附属台州医院(浙江省台州医院) |
通讯作者 | Wu, Jinming |
作者单位 | 1.Department of Gastroenterology,The First Affiliated Hospital of Wenzhou Medical University,Wenzhou,325000,China; 2.Department of Gastroenterology,The Affiliated Taizhou Hospital of Wenzhou Medical University,Taizhou,318000,China |
第一作者单位 | 附属第一医院; 第一临床医学院(信息与工程学院)、附属第一医院 |
通讯作者单位 | 附属第一医院; 第一临床医学院(信息与工程学院)、附属第一医院 |
第一作者的第一单位 | 附属第一医院 |
推荐引用方式 GB/T 7714 | Zheng, Juzeng,Ou, Zhanfan,Lin, Xianfan,et al. Analysis of epitope-based vaccine candidates against the E antigen of the hepatitis B virus based on the B genotype sequence: An in silico and in vitro approach[J]. CELLULAR IMMUNOLOGY,2018,329:56-65. |
APA | Zheng, Juzeng., Ou, Zhanfan., Lin, Xianfan., Wang, Lingling., Liu, Yang., ... & Wu, Jinming. (2018). Analysis of epitope-based vaccine candidates against the E antigen of the hepatitis B virus based on the B genotype sequence: An in silico and in vitro approach. CELLULAR IMMUNOLOGY, 329, 56-65. |
MLA | Zheng, Juzeng,et al."Analysis of epitope-based vaccine candidates against the E antigen of the hepatitis B virus based on the B genotype sequence: An in silico and in vitro approach".CELLULAR IMMUNOLOGY 329(2018):56-65. |
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