Cytotoxic T lymphocytes and CD4 epitope mutations in the pre-core/core region of hepatitis B virus in chronic hepatitis B carriers in Northeast Iran.
- Publisher:
- Springer
- Publication Type:
- Journal Article
- Citation:
- Indian Journal of Gastroenterology, 2017, 36, (4), pp. 253-257
- Issue Date:
- 2017-07
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Zhand, S | |
dc.contributor.author | Tabarraei, A | |
dc.contributor.author | Nazari, A | |
dc.contributor.author | Moradi, A | |
dc.date.accessioned | 2022-08-26T05:22:00Z | |
dc.date.available | 2017-06-30 | |
dc.date.available | 2022-08-26T05:22:00Z | |
dc.date.issued | 2017-07 | |
dc.identifier.citation | Indian Journal of Gastroenterology, 2017, 36, (4), pp. 253-257 | |
dc.identifier.issn | 0254-8860 | |
dc.identifier.issn | 0975-0711 | |
dc.identifier.uri | http://hdl.handle.net/10453/160905 | |
dc.description.abstract | BACKGROUNDS: Hepatitis B virus (HBV) is vulnerable to many various mutations. Those within epitopes recognized by sensitized T cells may influence the re-emergence of the virus. This study was designed to investigate the mutation in immune epitope regions of HBV pre-core/core among chronic HBV patients of Golestan province, Northeast Iran. METHODS: In 120 chronic HBV carriers, HBV DNA was extracted from blood plasma samples and PCR was done using specific primers. Direct sequencing and alignment of the pre-core/core region were applied using reference sequence from Gene Bank database (Accession Number AB033559). RESULTS: The study showed 27 inferred amino acid substitutions, 9 of which (33.3%) were in CD4 and 2 (7.4%) in cytotoxic T lymphocytes' (CTL) epitopes and 16 other mutations (59.2%) were observed in other regions. CONCLUSIONS: CTL escape mutations were not commonly observed in pre-core/core sequences of chronic HBV carriers in the locale of study. It can be concluded that most of the inferred amino acid substitutions occur in different immune epitopes other than CTL and CD4. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | Springer | |
dc.relation.ispartof | Indian Journal of Gastroenterology | |
dc.relation.isbasedon | 10.1007/s12664-017-0767-z | |
dc.rights | info:eu-repo/semantics/closedAccess | |
dc.subject | 1103 Clinical Sciences | |
dc.subject.mesh | Amino Acid Substitution | |
dc.subject.mesh | Carrier State | |
dc.subject.mesh | CD4 Antigens | |
dc.subject.mesh | Epitopes | |
dc.subject.mesh | Hepatitis B virus | |
dc.subject.mesh | Hepatitis B, Chronic | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Iran | |
dc.subject.mesh | Point Mutation | |
dc.subject.mesh | T-Lymphocytes, Cytotoxic | |
dc.subject.mesh | Amino Acid Substitution | |
dc.subject.mesh | CD4 Antigens | |
dc.subject.mesh | Carrier State | |
dc.subject.mesh | Epitopes | |
dc.subject.mesh | Hepatitis B virus | |
dc.subject.mesh | Hepatitis B, Chronic | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Iran | |
dc.subject.mesh | Point Mutation | |
dc.subject.mesh | T-Lymphocytes, Cytotoxic | |
dc.subject.mesh | T-Lymphocytes, Cytotoxic | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Hepatitis B virus | |
dc.subject.mesh | Hepatitis B, Chronic | |
dc.subject.mesh | Epitopes | |
dc.subject.mesh | Amino Acid Substitution | |
dc.subject.mesh | Carrier State | |
dc.subject.mesh | Point Mutation | |
dc.subject.mesh | Iran | |
dc.subject.mesh | CD4 Antigens | |
dc.title | Cytotoxic T lymphocytes and CD4 epitope mutations in the pre-core/core region of hepatitis B virus in chronic hepatitis B carriers in Northeast Iran. | |
dc.type | Journal Article | |
utslib.citation.volume | 36 | |
utslib.location.activity | India | |
utslib.for | 1103 Clinical Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
utslib.copyright.status | closed_access | * |
pubs.consider-herdc | false | |
dc.date.updated | 2022-08-26T05:21:58Z | |
pubs.issue | 4 | |
pubs.publication-status | Published | |
pubs.volume | 36 | |
utslib.citation.issue | 4 |
Abstract:
BACKGROUNDS: Hepatitis B virus (HBV) is vulnerable to many various mutations. Those within epitopes recognized by sensitized T cells may influence the re-emergence of the virus. This study was designed to investigate the mutation in immune epitope regions of HBV pre-core/core among chronic HBV patients of Golestan province, Northeast Iran. METHODS: In 120 chronic HBV carriers, HBV DNA was extracted from blood plasma samples and PCR was done using specific primers. Direct sequencing and alignment of the pre-core/core region were applied using reference sequence from Gene Bank database (Accession Number AB033559). RESULTS: The study showed 27 inferred amino acid substitutions, 9 of which (33.3%) were in CD4 and 2 (7.4%) in cytotoxic T lymphocytes' (CTL) epitopes and 16 other mutations (59.2%) were observed in other regions. CONCLUSIONS: CTL escape mutations were not commonly observed in pre-core/core sequences of chronic HBV carriers in the locale of study. It can be concluded that most of the inferred amino acid substitutions occur in different immune epitopes other than CTL and CD4.
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