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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.
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.
Afiliación
  • Brumeanu TD; Uniformed Services University of the Health Sciences, Department of Medicine, Division of Immunology, Bethesda, MD 20814, U.S.A.
  • Vir P; Uniformed Services University of the Health Sciences, Department of Medicine, Division of Immunology, Bethesda, MD 20814, U.S.A.
  • Karim AF; Uniformed Services University of the Health Sciences, Department of Medicine, Division of Immunology, Bethesda, MD 20814, U.S.A.
  • Kar S; Bioqual Inc., Rockville, MD 20852, U.S.A.
  • Benetiene D; Bioqual Inc., Rockville, MD 20852, U.S.A.
  • Lok M; Bioqual Inc., Rockville, MD 20852, U.S.A.
  • Greenhouse J; Bioqual Inc., Rockville, MD 20852, U.S.A.
  • Putmon-Taylor T; Bioqual Inc., Rockville, MD 20852, U.S.A.
  • Kitajewski C; Bioqual Inc., Rockville, MD 20852, U.S.A.
  • Chung KK; Uniformed Services University of the Health Sciences, Department of Medicine, Division of Immunology, Bethesda, MD 20814, U.S.A.
  • Pratt KP; Uniformed Services University of the Health Sciences, Department of Medicine, Division of Immunology, Bethesda, MD 20814, U.S.A.
  • Casares SA; Uniformed Services University of the Health Sciences, Department of Medicine, Division of Immunology, Bethesda, MD 20814, U.S.A.
bioRxiv ; 2021 Jan 29.
Article en En | MEDLINE | ID: mdl-32839773
ABSTRACT
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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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos