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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2021
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.
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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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