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The protection of CoronaVac against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant in nude‐hACE2 mice
BACKGROUND: Immunocompromised individuals have an increased risk of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection and severe outcomes, but we pay less attention to these people. Athymic nude mice are a murine strain with a spontaneous deficiency of the Foxn1 gene, which can...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10486324/ https://www.ncbi.nlm.nih.gov/pubmed/37431213 http://dx.doi.org/10.1002/ame2.12336 |
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author | Lin, Kaili Liu, Meixuan Sun, Lu Fu, Hanjun Qiao, Hongwei Wang, Shunyi Pan, Sidan Gao, Hong |
author_facet | Lin, Kaili Liu, Meixuan Sun, Lu Fu, Hanjun Qiao, Hongwei Wang, Shunyi Pan, Sidan Gao, Hong |
author_sort | Lin, Kaili |
collection | PubMed |
description | BACKGROUND: Immunocompromised individuals have an increased risk of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection and severe outcomes, but we pay less attention to these people. Athymic nude mice are a murine strain with a spontaneous deficiency of the Foxn1 gene, which can result in thymic degeneration or its absence, leading to immunosuppression and a decrease in the number of T cells, and are widely used in preclinical evaluations of disease in immunocompromised populations. METHODS: We investigated the protection of the coronavirus disease 2019 (COVID‐19) inactivated vaccine (CoronaVac) against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant utilizing a hybrid‐type nude‐hACE2 mouse model. RESULTS: Compared with nude‐hACE2/W mice, the viral load in the brain and lung tissue of nude‐hACE2 mice (nude‐hACE2/WV) infected with WH‐09 after vaccination significantly decreased, and the histopathological changes were also reduced. The viral load in the brain and lung tissue of nude‐hACE2 mice (nude‐hACE2/OV) infected with the Omicron variant after vaccination was lower than that in nude‐hACE2/O, but histopathological symptoms did not improve significantly. CONCLUSION: CoronaVac provides some protection against infection of both WH‐09 and the Omicron variant in the nude‐hACE2 mice. Our findings aimed to provide a reference for vaccination against SARS‐CoV‐2 in immunocompromised populations. |
format | Online Article Text |
id | pubmed-10486324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104863242023-09-09 The protection of CoronaVac against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant in nude‐hACE2 mice Lin, Kaili Liu, Meixuan Sun, Lu Fu, Hanjun Qiao, Hongwei Wang, Shunyi Pan, Sidan Gao, Hong Animal Model Exp Med Regular Articles BACKGROUND: Immunocompromised individuals have an increased risk of severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection and severe outcomes, but we pay less attention to these people. Athymic nude mice are a murine strain with a spontaneous deficiency of the Foxn1 gene, which can result in thymic degeneration or its absence, leading to immunosuppression and a decrease in the number of T cells, and are widely used in preclinical evaluations of disease in immunocompromised populations. METHODS: We investigated the protection of the coronavirus disease 2019 (COVID‐19) inactivated vaccine (CoronaVac) against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant utilizing a hybrid‐type nude‐hACE2 mouse model. RESULTS: Compared with nude‐hACE2/W mice, the viral load in the brain and lung tissue of nude‐hACE2 mice (nude‐hACE2/WV) infected with WH‐09 after vaccination significantly decreased, and the histopathological changes were also reduced. The viral load in the brain and lung tissue of nude‐hACE2 mice (nude‐hACE2/OV) infected with the Omicron variant after vaccination was lower than that in nude‐hACE2/O, but histopathological symptoms did not improve significantly. CONCLUSION: CoronaVac provides some protection against infection of both WH‐09 and the Omicron variant in the nude‐hACE2 mice. Our findings aimed to provide a reference for vaccination against SARS‐CoV‐2 in immunocompromised populations. John Wiley and Sons Inc. 2023-07-10 /pmc/articles/PMC10486324/ /pubmed/37431213 http://dx.doi.org/10.1002/ame2.12336 Text en © 2023 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Regular Articles Lin, Kaili Liu, Meixuan Sun, Lu Fu, Hanjun Qiao, Hongwei Wang, Shunyi Pan, Sidan Gao, Hong The protection of CoronaVac against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant in nude‐hACE2 mice |
title | The protection of CoronaVac against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant in nude‐hACE2 mice |
title_full | The protection of CoronaVac against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant in nude‐hACE2 mice |
title_fullStr | The protection of CoronaVac against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant in nude‐hACE2 mice |
title_full_unstemmed | The protection of CoronaVac against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant in nude‐hACE2 mice |
title_short | The protection of CoronaVac against the infection of wild‐type SARS‐CoV‐2 (WH‐09) or Omicron variant in nude‐hACE2 mice |
title_sort | protection of coronavac against the infection of wild‐type sars‐cov‐2 (wh‐09) or omicron variant in nude‐hace2 mice |
topic | Regular Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10486324/ https://www.ncbi.nlm.nih.gov/pubmed/37431213 http://dx.doi.org/10.1002/ame2.12336 |
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