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Development of a Humanized HLA-A2.1/DP4 Transgenic Mouse Model and the Use of This Model to Map HLA-DP4-Restricted Epitopes of HBV Envelope Protein
A new homozygous humanized transgenic mouse strain, HLA-A2.1(+/+)HLA-DP4(+/+) hCD4(+/+)mCD4(−/−)IAβ(−/−)β2m(−/−) (HLA-A2/DP4), was obtained by crossing the previously characterized HLA-A2(+/+)β2m(−/−) (A2) mouse and our previously created HLA-DP4(+/+) hCD4(+/+)mCD4(−/−)IAβ(−/−) (DP4) mouse. We confi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293898/ https://www.ncbi.nlm.nih.gov/pubmed/22403638 http://dx.doi.org/10.1371/journal.pone.0032247 |
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author | Ru, Zhitao Xiao, Wenjun Pajot, Anthony Kou, Zhihua Sun, Shihui Maillere, Bernard Zhao, Guangyu Ojcius, David M. Lone, Yu-chun Zhou, Yusen |
author_facet | Ru, Zhitao Xiao, Wenjun Pajot, Anthony Kou, Zhihua Sun, Shihui Maillere, Bernard Zhao, Guangyu Ojcius, David M. Lone, Yu-chun Zhou, Yusen |
author_sort | Ru, Zhitao |
collection | PubMed |
description | A new homozygous humanized transgenic mouse strain, HLA-A2.1(+/+)HLA-DP4(+/+) hCD4(+/+)mCD4(−/−)IAβ(−/−)β2m(−/−) (HLA-A2/DP4), was obtained by crossing the previously characterized HLA-A2(+/+)β2m(−/−) (A2) mouse and our previously created HLA-DP4(+/+) hCD4(+/+)mCD4(−/−)IAβ(−/−) (DP4) mouse. We confirmed that the transgenes (HLA-A2, HLA-DP4, hCD4) inherited from the parental A2 and DP4 mice are functional in the HLA-A2/DP4 mice. After immunizing HLA-A2/DP4 mice with a hepatitis B DNA vaccine, hepatitis B virus-specific antibodies, HLA-A2-restricted and HLA-DP4-restricted responses were observed to be similar to those in naturally infected humans. Therefore, the present study demonstrated that HLA-A2/DP4 transgenic mice can faithfully mimic human cellular responses. Furthermore, we reported four new HLA-DP4-restricted epitopes derived from HBsAg that were identified in both vaccinated HLA-A2/DP4 mice and HLA-DP4-positive human individuals. The HLA-A2/DP4 mouse model is a promising preclinical animal model carrying alleles present to more than a quarter of the human population. This model should facilitate the identification of novel HLA-A2- and HLA-DP4-restricted epitopes and vaccine development as well as the characterization of HLA-DP4-restricted responses against infection in humans. |
format | Online Article Text |
id | pubmed-3293898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32938982012-03-08 Development of a Humanized HLA-A2.1/DP4 Transgenic Mouse Model and the Use of This Model to Map HLA-DP4-Restricted Epitopes of HBV Envelope Protein Ru, Zhitao Xiao, Wenjun Pajot, Anthony Kou, Zhihua Sun, Shihui Maillere, Bernard Zhao, Guangyu Ojcius, David M. Lone, Yu-chun Zhou, Yusen PLoS One Research Article A new homozygous humanized transgenic mouse strain, HLA-A2.1(+/+)HLA-DP4(+/+) hCD4(+/+)mCD4(−/−)IAβ(−/−)β2m(−/−) (HLA-A2/DP4), was obtained by crossing the previously characterized HLA-A2(+/+)β2m(−/−) (A2) mouse and our previously created HLA-DP4(+/+) hCD4(+/+)mCD4(−/−)IAβ(−/−) (DP4) mouse. We confirmed that the transgenes (HLA-A2, HLA-DP4, hCD4) inherited from the parental A2 and DP4 mice are functional in the HLA-A2/DP4 mice. After immunizing HLA-A2/DP4 mice with a hepatitis B DNA vaccine, hepatitis B virus-specific antibodies, HLA-A2-restricted and HLA-DP4-restricted responses were observed to be similar to those in naturally infected humans. Therefore, the present study demonstrated that HLA-A2/DP4 transgenic mice can faithfully mimic human cellular responses. Furthermore, we reported four new HLA-DP4-restricted epitopes derived from HBsAg that were identified in both vaccinated HLA-A2/DP4 mice and HLA-DP4-positive human individuals. The HLA-A2/DP4 mouse model is a promising preclinical animal model carrying alleles present to more than a quarter of the human population. This model should facilitate the identification of novel HLA-A2- and HLA-DP4-restricted epitopes and vaccine development as well as the characterization of HLA-DP4-restricted responses against infection in humans. Public Library of Science 2012-03-05 /pmc/articles/PMC3293898/ /pubmed/22403638 http://dx.doi.org/10.1371/journal.pone.0032247 Text en Ru et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Ru, Zhitao Xiao, Wenjun Pajot, Anthony Kou, Zhihua Sun, Shihui Maillere, Bernard Zhao, Guangyu Ojcius, David M. Lone, Yu-chun Zhou, Yusen Development of a Humanized HLA-A2.1/DP4 Transgenic Mouse Model and the Use of This Model to Map HLA-DP4-Restricted Epitopes of HBV Envelope Protein |
title | Development of a Humanized HLA-A2.1/DP4 Transgenic Mouse Model and the Use of This Model to Map HLA-DP4-Restricted Epitopes of HBV Envelope Protein |
title_full | Development of a Humanized HLA-A2.1/DP4 Transgenic Mouse Model and the Use of This Model to Map HLA-DP4-Restricted Epitopes of HBV Envelope Protein |
title_fullStr | Development of a Humanized HLA-A2.1/DP4 Transgenic Mouse Model and the Use of This Model to Map HLA-DP4-Restricted Epitopes of HBV Envelope Protein |
title_full_unstemmed | Development of a Humanized HLA-A2.1/DP4 Transgenic Mouse Model and the Use of This Model to Map HLA-DP4-Restricted Epitopes of HBV Envelope Protein |
title_short | Development of a Humanized HLA-A2.1/DP4 Transgenic Mouse Model and the Use of This Model to Map HLA-DP4-Restricted Epitopes of HBV Envelope Protein |
title_sort | development of a humanized hla-a2.1/dp4 transgenic mouse model and the use of this model to map hla-dp4-restricted epitopes of hbv envelope protein |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293898/ https://www.ncbi.nlm.nih.gov/pubmed/22403638 http://dx.doi.org/10.1371/journal.pone.0032247 |
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