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High resolution HLA-DRB1 analysis and shared molecular amino acid signature of DRβ1 molecules in Occult hepatitis B infection
AIM: To investigate the association of human leukocyte antigen (HLA)-DRB1 alleles and the variations of polymorphic amino acid changes in DRβ1 chain in Shaanxi Han population with Occult hepatitis B infection (OBI). METHODS: High-resolution HLA-DRB1 genotyping was performed in 107 OBI carriers and 2...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040378/ https://www.ncbi.nlm.nih.gov/pubmed/35468727 http://dx.doi.org/10.1186/s12865-022-00496-2 |
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author | Wang, Tianju Shen, Chunmei Li, Hengxin Chen, Liping Liu, Sheng Qi, Jun |
author_facet | Wang, Tianju Shen, Chunmei Li, Hengxin Chen, Liping Liu, Sheng Qi, Jun |
author_sort | Wang, Tianju |
collection | PubMed |
description | AIM: To investigate the association of human leukocyte antigen (HLA)-DRB1 alleles and the variations of polymorphic amino acid changes in DRβ1 chain in Shaanxi Han population with Occult hepatitis B infection (OBI). METHODS: High-resolution HLA-DRB1 genotyping was performed in 107 OBI carriers and 280 normal controls. Sequence information was used to assign which amino acids were encoded at all polymorphic positions. Three-dimensional modeling was performed to explore the effect of the key residues on the HLA-DRB1 molecule. RESULTS: Strong susceptible association for allele DRB1*07:01 was observed in OBI carriers. The amino acid variation at HLA-DRβ1 molecule revealed susceptible associations for residues Gln(4β), Val(57β)(P9), Ser(60β)(P9) and Val(78β)(P4), the amino acids Arg(4β), Asp(57β)(P9), Tyr(60β)(P9) and Tyr(78β)(P4) showed protective associations. CONCLUSION: Alleles DRB1*07:01 showed strong susceptible associations in OBI carriers. The amino acid variations in DRβ molecules revealed significant molecular markers for susceptibility and protection from OBI in Shaanxi Han population. |
format | Online Article Text |
id | pubmed-9040378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90403782022-04-27 High resolution HLA-DRB1 analysis and shared molecular amino acid signature of DRβ1 molecules in Occult hepatitis B infection Wang, Tianju Shen, Chunmei Li, Hengxin Chen, Liping Liu, Sheng Qi, Jun BMC Immunol Article AIM: To investigate the association of human leukocyte antigen (HLA)-DRB1 alleles and the variations of polymorphic amino acid changes in DRβ1 chain in Shaanxi Han population with Occult hepatitis B infection (OBI). METHODS: High-resolution HLA-DRB1 genotyping was performed in 107 OBI carriers and 280 normal controls. Sequence information was used to assign which amino acids were encoded at all polymorphic positions. Three-dimensional modeling was performed to explore the effect of the key residues on the HLA-DRB1 molecule. RESULTS: Strong susceptible association for allele DRB1*07:01 was observed in OBI carriers. The amino acid variation at HLA-DRβ1 molecule revealed susceptible associations for residues Gln(4β), Val(57β)(P9), Ser(60β)(P9) and Val(78β)(P4), the amino acids Arg(4β), Asp(57β)(P9), Tyr(60β)(P9) and Tyr(78β)(P4) showed protective associations. CONCLUSION: Alleles DRB1*07:01 showed strong susceptible associations in OBI carriers. The amino acid variations in DRβ molecules revealed significant molecular markers for susceptibility and protection from OBI in Shaanxi Han population. BioMed Central 2022-04-25 /pmc/articles/PMC9040378/ /pubmed/35468727 http://dx.doi.org/10.1186/s12865-022-00496-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Article Wang, Tianju Shen, Chunmei Li, Hengxin Chen, Liping Liu, Sheng Qi, Jun High resolution HLA-DRB1 analysis and shared molecular amino acid signature of DRβ1 molecules in Occult hepatitis B infection |
title | High resolution HLA-DRB1 analysis and shared molecular amino acid signature of DRβ1 molecules in Occult hepatitis B infection |
title_full | High resolution HLA-DRB1 analysis and shared molecular amino acid signature of DRβ1 molecules in Occult hepatitis B infection |
title_fullStr | High resolution HLA-DRB1 analysis and shared molecular amino acid signature of DRβ1 molecules in Occult hepatitis B infection |
title_full_unstemmed | High resolution HLA-DRB1 analysis and shared molecular amino acid signature of DRβ1 molecules in Occult hepatitis B infection |
title_short | High resolution HLA-DRB1 analysis and shared molecular amino acid signature of DRβ1 molecules in Occult hepatitis B infection |
title_sort | high resolution hla-drb1 analysis and shared molecular amino acid signature of drβ1 molecules in occult hepatitis b infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9040378/ https://www.ncbi.nlm.nih.gov/pubmed/35468727 http://dx.doi.org/10.1186/s12865-022-00496-2 |
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