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Novel ACE2-IgG1 fusions with improved in vitro and in vivo activity against SARS-CoV2
SARS-CoV2, the etiologic agent of COVID-19, uses ACE2 as a cell entry receptor. Soluble ACE2 has been shown to have neutralizing antiviral activity but has a short half-life and no active transport mechanism from the circulation into the alveolar spaces of the lung. To overcome this, we constructed...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310620/ https://www.ncbi.nlm.nih.gov/pubmed/32587964 http://dx.doi.org/10.1101/2020.06.15.152157 |
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author | Iwanaga, Naoki Cooper, Laura Rong, Lijun Beddingfield, Brandon Crabtree, Jackelyn Tripp, Ralph A. Qin, Xuebin Kolls, Jay K. |
author_facet | Iwanaga, Naoki Cooper, Laura Rong, Lijun Beddingfield, Brandon Crabtree, Jackelyn Tripp, Ralph A. Qin, Xuebin Kolls, Jay K. |
author_sort | Iwanaga, Naoki |
collection | PubMed |
description | SARS-CoV2, the etiologic agent of COVID-19, uses ACE2 as a cell entry receptor. Soluble ACE2 has been shown to have neutralizing antiviral activity but has a short half-life and no active transport mechanism from the circulation into the alveolar spaces of the lung. To overcome this, we constructed an ACE2-human IgG1 fusion protein with mutations in the catalytic domain of ACE2. This fusion protein contained a LALA mutation that abrogates Fcrγ binding, but retains FcRN binding to prolong the half-life, as well as achieve therapeutic concentrations in the lung lavage. Interestingly, a mutation in the catalytic domain of ACE2, MDR504, completely abrogated catalytic activity, but significantly increased binding to SARS-CoV2 spike protein in vitro. This feature correlated with more potent viral neutralization in a plaque assay. Parental administration of the protein showed stable serum concentrations with a serum half-life of ~ 145 hours with excellent bioavailability in the epithelial lining fluid of the lung. Prophylactic administration of MDR504 significantly attenuated SARS-CoV2 infection in a murine model. These data support that the MDR504 hACE2-Fc is an excellent candidate for pre or post-exposure prophylaxis or treatment of COVID-19. |
format | Online Article Text |
id | pubmed-7310620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-73106202020-06-25 Novel ACE2-IgG1 fusions with improved in vitro and in vivo activity against SARS-CoV2 Iwanaga, Naoki Cooper, Laura Rong, Lijun Beddingfield, Brandon Crabtree, Jackelyn Tripp, Ralph A. Qin, Xuebin Kolls, Jay K. bioRxiv Article SARS-CoV2, the etiologic agent of COVID-19, uses ACE2 as a cell entry receptor. Soluble ACE2 has been shown to have neutralizing antiviral activity but has a short half-life and no active transport mechanism from the circulation into the alveolar spaces of the lung. To overcome this, we constructed an ACE2-human IgG1 fusion protein with mutations in the catalytic domain of ACE2. This fusion protein contained a LALA mutation that abrogates Fcrγ binding, but retains FcRN binding to prolong the half-life, as well as achieve therapeutic concentrations in the lung lavage. Interestingly, a mutation in the catalytic domain of ACE2, MDR504, completely abrogated catalytic activity, but significantly increased binding to SARS-CoV2 spike protein in vitro. This feature correlated with more potent viral neutralization in a plaque assay. Parental administration of the protein showed stable serum concentrations with a serum half-life of ~ 145 hours with excellent bioavailability in the epithelial lining fluid of the lung. Prophylactic administration of MDR504 significantly attenuated SARS-CoV2 infection in a murine model. These data support that the MDR504 hACE2-Fc is an excellent candidate for pre or post-exposure prophylaxis or treatment of COVID-19. Cold Spring Harbor Laboratory 2020-07-24 /pmc/articles/PMC7310620/ /pubmed/32587964 http://dx.doi.org/10.1101/2020.06.15.152157 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/It is made available under a CC-BY-NC-ND 4.0 International license (http://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Article Iwanaga, Naoki Cooper, Laura Rong, Lijun Beddingfield, Brandon Crabtree, Jackelyn Tripp, Ralph A. Qin, Xuebin Kolls, Jay K. Novel ACE2-IgG1 fusions with improved in vitro and in vivo activity against SARS-CoV2 |
title | Novel ACE2-IgG1 fusions with improved in vitro and in vivo activity against SARS-CoV2 |
title_full | Novel ACE2-IgG1 fusions with improved in vitro and in vivo activity against SARS-CoV2 |
title_fullStr | Novel ACE2-IgG1 fusions with improved in vitro and in vivo activity against SARS-CoV2 |
title_full_unstemmed | Novel ACE2-IgG1 fusions with improved in vitro and in vivo activity against SARS-CoV2 |
title_short | Novel ACE2-IgG1 fusions with improved in vitro and in vivo activity against SARS-CoV2 |
title_sort | novel ace2-igg1 fusions with improved in vitro and in vivo activity against sars-cov2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7310620/ https://www.ncbi.nlm.nih.gov/pubmed/32587964 http://dx.doi.org/10.1101/2020.06.15.152157 |
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