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A Human-Immune-System (HIS) humanized mouse model (DRAGA: HLA-A2. HLA-DR4. Rag1 KO.IL-2Rγc KO. NOD) for COVID-19
We report the first Human Immune System (HIS)-humanized mouse model (“DRAGA”: HLA-A2.HLA-DR4.Rag1KO.IL-2RγcKO.NOD) for COVID-19 research. This mouse is reconstituted with human cord blood-derived, HLA-matched hematopoietic stem cells. It engrafts human epi/endothelial cells expressing the human ACE2...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444284/ https://www.ncbi.nlm.nih.gov/pubmed/32839773 http://dx.doi.org/10.1101/2020.08.19.251249 |
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author | Brumeanu, Teodor-D. Vir, Pooja Karim, Ahmad Faisal Kar, Swagata Benetiene, Dalia Lok, Megan Greenhouse, Jack Putmon-Taylor, Tammy Kitajewski, Christopher Chung, Kevin K. Pratt, Kathleen P. Casares, Sofia A. |
author_facet | Brumeanu, Teodor-D. Vir, Pooja Karim, Ahmad Faisal Kar, Swagata Benetiene, Dalia Lok, Megan Greenhouse, Jack Putmon-Taylor, Tammy Kitajewski, Christopher Chung, Kevin K. Pratt, Kathleen P. Casares, Sofia A. |
author_sort | Brumeanu, Teodor-D. |
collection | PubMed |
description | We report the first Human Immune System (HIS)-humanized mouse model (“DRAGA”: HLA-A2.HLA-DR4.Rag1KO.IL-2RγcKO.NOD) for COVID-19 research. This mouse is reconstituted with human cord blood-derived, HLA-matched hematopoietic stem cells. It engrafts human epi/endothelial cells expressing the human ACE2 receptor for SARS-CoV-2 and TMPRSS2 serine protease co-localized on lung epithelia. HIS-DRAGA mice sustained SARS-CoV-2 infection, showing deteriorated clinical condition, replicating virus in the lungs, and human-like lung immunopathology including T-cell infiltrates, microthrombi and pulmonary sequelae. Among T-cell infiltrates, lung-resident (CD103(+)) CD8(+) T cells were sequestered in epithelial (CD326(+)) lung niches and secreted granzyme B and perforin, indicating cytotoxic potential. Infected mice also developed antibodies against the SARS-CoV-2 viral proteins. Hence, HIS-DRAGA mice showed unique advantages as a surrogate in vivo human model for studying SARS-CoV-2 immunopathology and for testing the safety and efficacy of candidate vaccines and therapeutics. |
format | Online Article Text |
id | pubmed-7444284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-74442842020-08-25 A Human-Immune-System (HIS) humanized mouse model (DRAGA: HLA-A2. HLA-DR4. Rag1 KO.IL-2Rγc KO. NOD) for COVID-19 Brumeanu, Teodor-D. Vir, Pooja Karim, Ahmad Faisal Kar, Swagata Benetiene, Dalia Lok, Megan Greenhouse, Jack Putmon-Taylor, Tammy Kitajewski, Christopher Chung, Kevin K. Pratt, Kathleen P. Casares, Sofia A. bioRxiv Article We report the first Human Immune System (HIS)-humanized mouse model (“DRAGA”: HLA-A2.HLA-DR4.Rag1KO.IL-2RγcKO.NOD) for COVID-19 research. This mouse is reconstituted with human cord blood-derived, HLA-matched hematopoietic stem cells. It engrafts human epi/endothelial cells expressing the human ACE2 receptor for SARS-CoV-2 and TMPRSS2 serine protease co-localized on lung epithelia. HIS-DRAGA mice sustained SARS-CoV-2 infection, showing deteriorated clinical condition, replicating virus in the lungs, and human-like lung immunopathology including T-cell infiltrates, microthrombi and pulmonary sequelae. Among T-cell infiltrates, lung-resident (CD103(+)) CD8(+) T cells were sequestered in epithelial (CD326(+)) lung niches and secreted granzyme B and perforin, indicating cytotoxic potential. Infected mice also developed antibodies against the SARS-CoV-2 viral proteins. Hence, HIS-DRAGA mice showed unique advantages as a surrogate in vivo human model for studying SARS-CoV-2 immunopathology and for testing the safety and efficacy of candidate vaccines and therapeutics. Cold Spring Harbor Laboratory 2021-01-29 /pmc/articles/PMC7444284/ /pubmed/32839773 http://dx.doi.org/10.1101/2020.08.19.251249 Text en https://creativecommons.org/publicdomain/zero/1.0/This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license (https://creativecommons.org/publicdomain/zero/1.0/) . |
spellingShingle | Article Brumeanu, Teodor-D. Vir, Pooja Karim, Ahmad Faisal Kar, Swagata Benetiene, Dalia Lok, Megan Greenhouse, Jack Putmon-Taylor, Tammy Kitajewski, Christopher Chung, Kevin K. Pratt, Kathleen P. Casares, Sofia A. A Human-Immune-System (HIS) humanized mouse model (DRAGA: HLA-A2. HLA-DR4. Rag1 KO.IL-2Rγc KO. NOD) for COVID-19 |
title | A Human-Immune-System (HIS) humanized mouse model (DRAGA: HLA-A2. HLA-DR4. Rag1 KO.IL-2Rγc KO. NOD) for COVID-19 |
title_full | A Human-Immune-System (HIS) humanized mouse model (DRAGA: HLA-A2. HLA-DR4. Rag1 KO.IL-2Rγc KO. NOD) for COVID-19 |
title_fullStr | A Human-Immune-System (HIS) humanized mouse model (DRAGA: HLA-A2. HLA-DR4. Rag1 KO.IL-2Rγc KO. NOD) for COVID-19 |
title_full_unstemmed | A Human-Immune-System (HIS) humanized mouse model (DRAGA: HLA-A2. HLA-DR4. Rag1 KO.IL-2Rγc KO. NOD) for COVID-19 |
title_short | A Human-Immune-System (HIS) humanized mouse model (DRAGA: HLA-A2. HLA-DR4. Rag1 KO.IL-2Rγc KO. NOD) for COVID-19 |
title_sort | human-immune-system (his) humanized mouse model (draga: hla-a2. hla-dr4. rag1 ko.il-2rγc ko. nod) for covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7444284/ https://www.ncbi.nlm.nih.gov/pubmed/32839773 http://dx.doi.org/10.1101/2020.08.19.251249 |
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