EGYVIR: An immunomodulatory herbal extract with potent antiviral activity against SARS-CoV-2
Due to the challenges for developing vaccines in devastating pandemic situations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), developing and screening of novel antiviral agents are peremptorily demanded. Herein, we developed EGYVIR as a potent immunomodulatory herbal extract with...
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Published in | PloS one Vol. 15; no. 11; p. e0241739 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
18.11.2020
Public Library of Science (PLoS) |
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Abstract | Due to the challenges for developing vaccines in devastating pandemic situations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), developing and screening of novel antiviral agents are peremptorily demanded. Herein, we developed EGYVIR as a potent immunomodulatory herbal extract with promising antiviral activity against SARS-CoV-2. It constitutes of a combination of black pepper extract with curcumin extract. The antiviral effect of EGYVIR extract is attributed to the two key phases of the disease in severe cases. First, the inhibition of the nuclear translocation of NF-kβ p50, attenuating the SARS-CoV-2 infection-associated cytokine storm. Additionally, the EGYVIR extract has an in vitro virucidal effect for SARS-CoV-2. The in vitro study of EGYVIR extract against SARS-CoV-2 on Huh-7 cell lines, revealed the potential role of NF-kβ/TNFα/IL-6 during the infection process. EGYVIR antagonizes the NF-kβ pathway
in-silico
and
in-vitro
studies. Consequently, it has the potential to hinder the release of IL-6 and TNFα, decreasing the production of essential cytokines storm elements. |
---|---|
AbstractList | Due to the challenges for developing vaccines in devastating pandemic situations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), developing and screening of novel antiviral agents are peremptorily demanded. Herein, we developed EGYVIR as a potent immunomodulatory herbal extract with promising antiviral activity against SARS-CoV-2. It constitutes of a combination of black pepper extract with curcumin extract. The antiviral effect of EGYVIR extract is attributed to the two key phases of the disease in severe cases. First, the inhibition of the nuclear translocation of NF-kβ p50, attenuating the SARS-CoV-2 infection-associated cytokine storm. Additionally, the EGYVIR extract has an in vitro virucidal effect for SARS-CoV-2. The in vitro study of EGYVIR extract against SARS-CoV-2 on Huh-7 cell lines, revealed the potential role of NF-kβ/TNFα/IL-6 during the infection process. EGYVIR antagonizes the NF-kβ pathway in-silico and in-vitro studies. Consequently, it has the potential to hinder the release of IL-6 and TNFα, decreasing the production of essential cytokines storm elements. Due to the challenges for developing vaccines in devastating pandemic situations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), developing and screening of novel antiviral agents are peremptorily demanded. Herein, we developed EGYVIR as a potent immunomodulatory herbal extract with promising antiviral activity against SARS-CoV-2. It constitutes of a combination of black pepper extract with curcumin extract. The antiviral effect of EGYVIR extract is attributed to the two key phases of the disease in severe cases. First, the inhibition of the nuclear translocation of NF-kβ p50, attenuating the SARS-CoV-2 infection-associated cytokine storm. Additionally, the EGYVIR extract has an in vitro virucidal effect for SARS-CoV-2. The in vitro study of EGYVIR extract against SARS-CoV-2 on Huh-7 cell lines, revealed the potential role of NF-kβ/TNFα/IL-6 during the infection process. EGYVIR antagonizes the NF-kβ pathway in-silico and in-vitro studies. Consequently, it has the potential to hinder the release of IL-6 and TNFα, decreasing the production of essential cytokines storm elements. Due to the challenges for developing vaccines in devastating pandemic situations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), developing and screening of novel antiviral agents are peremptorily demanded. Herein, we developed EGYVIR as a potent immunomodulatory herbal extract with promising antiviral activity against SARS-CoV-2. It constitutes of a combination of black pepper extract with curcumin extract. The antiviral effect of EGYVIR extract is attributed to the two key phases of the disease in severe cases. First, the inhibition of the nuclear translocation of NF-kβ p50, attenuating the SARS-CoV-2 infection-associated cytokine storm. Additionally, the EGYVIR extract has an in vitro virucidal effect for SARS-CoV-2. The in vitro study of EGYVIR extract against SARS-CoV-2 on Huh-7 cell lines, revealed the potential role of NF-kβ/TNFα/IL-6 during the infection process. EGYVIR antagonizes the NF-kβ pathway in-silico and in-vitro studies. Consequently, it has the potential to hinder the release of IL-6 and TNFα, decreasing the production of essential cytokines storm elements.Due to the challenges for developing vaccines in devastating pandemic situations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), developing and screening of novel antiviral agents are peremptorily demanded. Herein, we developed EGYVIR as a potent immunomodulatory herbal extract with promising antiviral activity against SARS-CoV-2. It constitutes of a combination of black pepper extract with curcumin extract. The antiviral effect of EGYVIR extract is attributed to the two key phases of the disease in severe cases. First, the inhibition of the nuclear translocation of NF-kβ p50, attenuating the SARS-CoV-2 infection-associated cytokine storm. Additionally, the EGYVIR extract has an in vitro virucidal effect for SARS-CoV-2. The in vitro study of EGYVIR extract against SARS-CoV-2 on Huh-7 cell lines, revealed the potential role of NF-kβ/TNFα/IL-6 during the infection process. EGYVIR antagonizes the NF-kβ pathway in-silico and in-vitro studies. Consequently, it has the potential to hinder the release of IL-6 and TNFα, decreasing the production of essential cytokines storm elements. Due to the challenges for developing vaccines in devastating pandemic situations of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), developing and screening of novel antiviral agents are peremptorily demanded. Herein, we developed EGYVIR as a potent immunomodulatory herbal extract with promising antiviral activity against SARS-CoV-2. It constitutes of a combination of black pepper extract with curcumin extract. The antiviral effect of EGYVIR extract is attributed to the two key phases of the disease in severe cases. First, the inhibition of the nuclear translocation of NF-k[beta] p50, attenuating the SARS-CoV-2 infection-associated cytokine storm. Additionally, the EGYVIR extract has an in vitro virucidal effect for SARS-CoV-2. The in vitro study of EGYVIR extract against SARS-CoV-2 on Huh-7 cell lines, revealed the potential role of NF-k[beta]/TNF[alpha]/IL-6 during the infection process. EGYVIR antagonizes the NF-k[beta] pathway in-silico and in-vitro studies. Consequently, it has the potential to hinder the release of IL-6 and TNF[alpha], decreasing the production of essential cytokines storm elements. |
Audience | Academic |
Author | Abo Shama, Noura M. Roshdy, Wael H. Moatasim, Yassmin El-Sayed, Ibrahim H. Kandeil, Ahmed Gomaa, Mokhtar R. El Guindy, Nancy M. Ali, Mohamed A. Naguib, Amal Kutkat, Omnia Rashed, Helmy A. Mostafa, Ahmed Kayali, Ghazi |
AuthorAffiliation | 2 Center of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt 5 Human Link, Baabda, Lebanon 4 Department of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas, Houston, Texas, United States of America 3 Biochemistry Department, Faculty of Science, Kafr El Sheikh University, Kafr El-Shaikh, Egypt University of Hong Kong, HONG KONG 1 Central Public Health Laboratory, Ministry of Health and Population, Cairo, Egypt |
AuthorAffiliation_xml | – name: University of Hong Kong, HONG KONG – name: 1 Central Public Health Laboratory, Ministry of Health and Population, Cairo, Egypt – name: 4 Department of Epidemiology, Human Genetics, and Environmental Sciences, University of Texas, Houston, Texas, United States of America – name: 2 Center of Scientific Excellence for Influenza Viruses, National Research Centre, Giza, Egypt – name: 3 Biochemistry Department, Faculty of Science, Kafr El Sheikh University, Kafr El-Shaikh, Egypt – name: 5 Human Link, Baabda, Lebanon |
Author_xml | – sequence: 1 givenname: Wael H. orcidid: 0000-0001-8412-3128 surname: Roshdy fullname: Roshdy, Wael H. – sequence: 2 givenname: Helmy A. surname: Rashed fullname: Rashed, Helmy A. – sequence: 3 givenname: Ahmed surname: Kandeil fullname: Kandeil, Ahmed – sequence: 4 givenname: Ahmed surname: Mostafa fullname: Mostafa, Ahmed – sequence: 5 givenname: Yassmin orcidid: 0000-0003-2159-2511 surname: Moatasim fullname: Moatasim, Yassmin – sequence: 6 givenname: Omnia surname: Kutkat fullname: Kutkat, Omnia – sequence: 7 givenname: Noura M. surname: Abo Shama fullname: Abo Shama, Noura M. – sequence: 8 givenname: Mokhtar R. surname: Gomaa fullname: Gomaa, Mokhtar R. – sequence: 9 givenname: Ibrahim H. surname: El-Sayed fullname: El-Sayed, Ibrahim H. – sequence: 10 givenname: Nancy M. surname: El Guindy fullname: El Guindy, Nancy M. – sequence: 11 givenname: Amal surname: Naguib fullname: Naguib, Amal – sequence: 12 givenname: Ghazi orcidid: 0000-0002-5387-1622 surname: Kayali fullname: Kayali, Ghazi – sequence: 13 givenname: Mohamed A. surname: Ali fullname: Ali, Mohamed A. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33206688$$D View this record in MEDLINE/PubMed |
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Copyright | COPYRIGHT 2020 Public Library of Science 2020 Roshdy et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2020 Roshdy et al 2020 Roshdy et al |
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