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Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells
Specific antibodies that humans acquire as a result of disease or after vaccination are needed to effectively suppress infection with a specific variant of SARS CoV-2 virus. The S protein of the D614G variant of coronavirus is used as an antigen in known vaccines to date. It is known that COVID-19 d...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s). Published by Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598048/ https://www.ncbi.nlm.nih.gov/pubmed/36313266 http://dx.doi.org/10.1016/j.mehy.2022.110965 |
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author | Siewiński, Maciej Bażanów, Barbara Orzechowska, Beata Gołąb, Krzysztof Gburek, Jakub Matkowski, Adam Rapak, Andrzej Janocha, Anna Krata, Lechosław Dobrzyński, Maciej Kilar, Ewa |
author_facet | Siewiński, Maciej Bażanów, Barbara Orzechowska, Beata Gołąb, Krzysztof Gburek, Jakub Matkowski, Adam Rapak, Andrzej Janocha, Anna Krata, Lechosław Dobrzyński, Maciej Kilar, Ewa |
author_sort | Siewiński, Maciej |
collection | PubMed |
description | Specific antibodies that humans acquire as a result of disease or after vaccination are needed to effectively suppress infection with a specific variant of SARS CoV-2 virus. The S protein of the D614G variant of coronavirus is used as an antigen in known vaccines to date. It is known that COVID-19 disease resulting from infection with this coronavirus can often be very dangerous to the health and lives of patients. In contrast, vaccines produce antibodies against an older version of the protein S-D614G (January 2020) and therefore have difficulty recognizing new variants of the virus. In our project we propose to obtain specific and precise antibodies by means of so-called controlled infection against specific infectious variants of the SARS-CoV-2 virus “here and now”. Currently, several variants of this pathogen have already emerged that threaten the health and lives of patients. We propose to reduce this threat by partially, but not completely, blocking the fusion mechanism of the SARS-CoV-2 virus into human respiratory cells. According to our plan, this can be achieved by inhibiting cathepsin L activity in respiratory cells, after introducing natural and non-toxic cysteine protease inhibitors into this area. We obtain these inhibitors by our own method from natural, “human body friendly” natural resources. We hypothesize that blocking cathepsin L will reduce the number of infecting viruses in cells to such an extent that COVID-19 developing in infected individuals will not threaten their health and life. At the same time, the number of viruses will be sufficient for the body's own immune system to produce precise antibodies against a specific version of this pathogen. |
format | Online Article Text |
id | pubmed-9598048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Author(s). Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95980482022-10-26 Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells Siewiński, Maciej Bażanów, Barbara Orzechowska, Beata Gołąb, Krzysztof Gburek, Jakub Matkowski, Adam Rapak, Andrzej Janocha, Anna Krata, Lechosław Dobrzyński, Maciej Kilar, Ewa Med Hypotheses Article Specific antibodies that humans acquire as a result of disease or after vaccination are needed to effectively suppress infection with a specific variant of SARS CoV-2 virus. The S protein of the D614G variant of coronavirus is used as an antigen in known vaccines to date. It is known that COVID-19 disease resulting from infection with this coronavirus can often be very dangerous to the health and lives of patients. In contrast, vaccines produce antibodies against an older version of the protein S-D614G (January 2020) and therefore have difficulty recognizing new variants of the virus. In our project we propose to obtain specific and precise antibodies by means of so-called controlled infection against specific infectious variants of the SARS-CoV-2 virus “here and now”. Currently, several variants of this pathogen have already emerged that threaten the health and lives of patients. We propose to reduce this threat by partially, but not completely, blocking the fusion mechanism of the SARS-CoV-2 virus into human respiratory cells. According to our plan, this can be achieved by inhibiting cathepsin L activity in respiratory cells, after introducing natural and non-toxic cysteine protease inhibitors into this area. We obtain these inhibitors by our own method from natural, “human body friendly” natural resources. We hypothesize that blocking cathepsin L will reduce the number of infecting viruses in cells to such an extent that COVID-19 developing in infected individuals will not threaten their health and life. At the same time, the number of viruses will be sufficient for the body's own immune system to produce precise antibodies against a specific version of this pathogen. The Author(s). Published by Elsevier Ltd. 2022-11 2022-10-26 /pmc/articles/PMC9598048/ /pubmed/36313266 http://dx.doi.org/10.1016/j.mehy.2022.110965 Text en © 2022 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Siewiński, Maciej Bażanów, Barbara Orzechowska, Beata Gołąb, Krzysztof Gburek, Jakub Matkowski, Adam Rapak, Andrzej Janocha, Anna Krata, Lechosław Dobrzyński, Maciej Kilar, Ewa Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells |
title | Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells |
title_full | Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells |
title_fullStr | Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells |
title_full_unstemmed | Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells |
title_short | Use of natural cysteine protease inhibitors in limiting SARS-Co-2 fusion into human respiratory cells |
title_sort | use of natural cysteine protease inhibitors in limiting sars-co-2 fusion into human respiratory cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9598048/ https://www.ncbi.nlm.nih.gov/pubmed/36313266 http://dx.doi.org/10.1016/j.mehy.2022.110965 |
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