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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 |
Sumario: | 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. |
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