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Efficacy of Plant-Made Human Recombinant ACE2 against COVID-19 in a Golden Syrian Hamster Model
Coronavirus disease 2019 (COVID-19) is a novel infectious respiratory disease caused by SARS-CoV-2. We evaluated the efficacy of a plant-based human recombinant angiotensin-converting enzyme 2 (hrACE2) and hrACE2-foldon (hrACE2-Fd) protein against COVID-19. In addition, we analyzed the antiviral act...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146983/ https://www.ncbi.nlm.nih.gov/pubmed/37112944 http://dx.doi.org/10.3390/v15040964 |
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author | Kim, Choon-Mee Kim, Dong-Min Bang, Mi-Seon Seo, Jun-Won Kim, Da-Young Yun, Na-Ra Lim, Sung-Chul Lee, Ju-Hyung Sohn, Eun-Ju Kang, Hyangju Min, Kyungmin Choi, Bo-Hwa Lee, Sangmin |
author_facet | Kim, Choon-Mee Kim, Dong-Min Bang, Mi-Seon Seo, Jun-Won Kim, Da-Young Yun, Na-Ra Lim, Sung-Chul Lee, Ju-Hyung Sohn, Eun-Ju Kang, Hyangju Min, Kyungmin Choi, Bo-Hwa Lee, Sangmin |
author_sort | Kim, Choon-Mee |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) is a novel infectious respiratory disease caused by SARS-CoV-2. We evaluated the efficacy of a plant-based human recombinant angiotensin-converting enzyme 2 (hrACE2) and hrACE2-foldon (hrACE2-Fd) protein against COVID-19. In addition, we analyzed the antiviral activity of hrACE2 and hrACE2-Fd against SARS-CoV-2 using real-time reverse-transcription PCR and plaque assays. The therapeutic efficacy was detected using the Golden Syrian hamster model infected with SARS-CoV-2. Both hrACE2 and hrACE2-Fd inhibited SARS-CoV-2 by 50% at concentrations below the maximum plasma concentration, with EC(50) of 5.8 μg/mL and 6.2 μg/mL, respectively. The hrACE2 and hrACE2-Fd injection groups showed a tendency for decreased viral titers in nasal turbinate tissues on day 3 after virus inoculation; however, this decrease was not detectable in lung tissues. Histopathological examination on day 9 after virus inoculation showed continued inflammation in the SARS-CoV-2 infection group, whereas decreased inflammation was observed in both the hrACE2 and hrACE2-Fd injection groups. No significant changes were observed at other time points. In conclusion, the potential therapeutic efficacy of plant-based proteins, hrACE2 and hrACE2-Fd, against COVID-19 was confirmed in a SARS-CoV-2-inoculated Golden Syrian hamster model. Further preclinical studies on primates and humans are necessary to obtain additional evidence and determine the effectiveness of these therapies. |
format | Online Article Text |
id | pubmed-10146983 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101469832023-04-29 Efficacy of Plant-Made Human Recombinant ACE2 against COVID-19 in a Golden Syrian Hamster Model Kim, Choon-Mee Kim, Dong-Min Bang, Mi-Seon Seo, Jun-Won Kim, Da-Young Yun, Na-Ra Lim, Sung-Chul Lee, Ju-Hyung Sohn, Eun-Ju Kang, Hyangju Min, Kyungmin Choi, Bo-Hwa Lee, Sangmin Viruses Article Coronavirus disease 2019 (COVID-19) is a novel infectious respiratory disease caused by SARS-CoV-2. We evaluated the efficacy of a plant-based human recombinant angiotensin-converting enzyme 2 (hrACE2) and hrACE2-foldon (hrACE2-Fd) protein against COVID-19. In addition, we analyzed the antiviral activity of hrACE2 and hrACE2-Fd against SARS-CoV-2 using real-time reverse-transcription PCR and plaque assays. The therapeutic efficacy was detected using the Golden Syrian hamster model infected with SARS-CoV-2. Both hrACE2 and hrACE2-Fd inhibited SARS-CoV-2 by 50% at concentrations below the maximum plasma concentration, with EC(50) of 5.8 μg/mL and 6.2 μg/mL, respectively. The hrACE2 and hrACE2-Fd injection groups showed a tendency for decreased viral titers in nasal turbinate tissues on day 3 after virus inoculation; however, this decrease was not detectable in lung tissues. Histopathological examination on day 9 after virus inoculation showed continued inflammation in the SARS-CoV-2 infection group, whereas decreased inflammation was observed in both the hrACE2 and hrACE2-Fd injection groups. No significant changes were observed at other time points. In conclusion, the potential therapeutic efficacy of plant-based proteins, hrACE2 and hrACE2-Fd, against COVID-19 was confirmed in a SARS-CoV-2-inoculated Golden Syrian hamster model. Further preclinical studies on primates and humans are necessary to obtain additional evidence and determine the effectiveness of these therapies. MDPI 2023-04-14 /pmc/articles/PMC10146983/ /pubmed/37112944 http://dx.doi.org/10.3390/v15040964 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kim, Choon-Mee Kim, Dong-Min Bang, Mi-Seon Seo, Jun-Won Kim, Da-Young Yun, Na-Ra Lim, Sung-Chul Lee, Ju-Hyung Sohn, Eun-Ju Kang, Hyangju Min, Kyungmin Choi, Bo-Hwa Lee, Sangmin Efficacy of Plant-Made Human Recombinant ACE2 against COVID-19 in a Golden Syrian Hamster Model |
title | Efficacy of Plant-Made Human Recombinant ACE2 against COVID-19 in a Golden Syrian Hamster Model |
title_full | Efficacy of Plant-Made Human Recombinant ACE2 against COVID-19 in a Golden Syrian Hamster Model |
title_fullStr | Efficacy of Plant-Made Human Recombinant ACE2 against COVID-19 in a Golden Syrian Hamster Model |
title_full_unstemmed | Efficacy of Plant-Made Human Recombinant ACE2 against COVID-19 in a Golden Syrian Hamster Model |
title_short | Efficacy of Plant-Made Human Recombinant ACE2 against COVID-19 in a Golden Syrian Hamster Model |
title_sort | efficacy of plant-made human recombinant ace2 against covid-19 in a golden syrian hamster model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10146983/ https://www.ncbi.nlm.nih.gov/pubmed/37112944 http://dx.doi.org/10.3390/v15040964 |
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