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Estrogen hormone is an essential sex factor inhibiting inflammation and immune response in COVID-19

Although vaccines have been evaluated and approved for SARS-CoV-2 infection prevention, there remains a lack of effective treatments to reduce the mortality of COVID-19 patients already infected with SARS-CoV-2. The global data of COVID-19 showed that men have a higher mortality rate than women. We...

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Autores principales: Li, Fuhai, Boon, Adrianus C.M., Michelson, Andrew P., Foraker, Randi E., Zhan, Ming, Payne, Philip R.O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491851/
https://www.ncbi.nlm.nih.gov/pubmed/34611658
http://dx.doi.org/10.21203/rs.3.rs-936900/v1
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author Li, Fuhai
Boon, Adrianus C.M.
Michelson, Andrew P.
Foraker, Randi E.
Zhan, Ming
Payne, Philip R.O.
author_facet Li, Fuhai
Boon, Adrianus C.M.
Michelson, Andrew P.
Foraker, Randi E.
Zhan, Ming
Payne, Philip R.O.
author_sort Li, Fuhai
collection PubMed
description Although vaccines have been evaluated and approved for SARS-CoV-2 infection prevention, there remains a lack of effective treatments to reduce the mortality of COVID-19 patients already infected with SARS-CoV-2. The global data of COVID-19 showed that men have a higher mortality rate than women. We further observed that the proportion of mortality of female increases starting from around the age of 55 significantly. Thus, sex is an essential factor associated with COVID-19 mortality, and sex related genetic factors could be interesting mechanisms and targets for COVID-19 treatment. However, the associated sex factors and signaling pathways remain unclear. Here, we propose to uncover the potential sex associated factors using systematic and integrative network analysis. The unique results indicated that estrogen hormones (ER), e.g., estrone and estriol, 1) interacting with ESR1/2 receptors, 2) can inhibit SARS-CoV-2 caused inflammation and immune response signaling in host cells; and 3) estrogen hormone is associated with the distinct fatality rates between male and female COVID-19 patients. Specifically, a high level of estradiol protecting young female COVID-19 patients, and estrogen loss to an extremely low level in females after about 55 years of age causing the increased fatality rate of women. In conclusion, estrogen hormone, interacting with ESR1/2 receptors, is an essential sex factor that protects COVID-19 patients by inhibiting inflammation and immune response caused by SARS-CoV-2 infection. Medications perturb the down-stream of ESR1/ESR2 to inhibit the inflammation and immune response can be effective or synergistic combined with other existing drugs for COVID-19 treatment.
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spelling pubmed-84918512021-10-06 Estrogen hormone is an essential sex factor inhibiting inflammation and immune response in COVID-19 Li, Fuhai Boon, Adrianus C.M. Michelson, Andrew P. Foraker, Randi E. Zhan, Ming Payne, Philip R.O. Res Sq Article Although vaccines have been evaluated and approved for SARS-CoV-2 infection prevention, there remains a lack of effective treatments to reduce the mortality of COVID-19 patients already infected with SARS-CoV-2. The global data of COVID-19 showed that men have a higher mortality rate than women. We further observed that the proportion of mortality of female increases starting from around the age of 55 significantly. Thus, sex is an essential factor associated with COVID-19 mortality, and sex related genetic factors could be interesting mechanisms and targets for COVID-19 treatment. However, the associated sex factors and signaling pathways remain unclear. Here, we propose to uncover the potential sex associated factors using systematic and integrative network analysis. The unique results indicated that estrogen hormones (ER), e.g., estrone and estriol, 1) interacting with ESR1/2 receptors, 2) can inhibit SARS-CoV-2 caused inflammation and immune response signaling in host cells; and 3) estrogen hormone is associated with the distinct fatality rates between male and female COVID-19 patients. Specifically, a high level of estradiol protecting young female COVID-19 patients, and estrogen loss to an extremely low level in females after about 55 years of age causing the increased fatality rate of women. In conclusion, estrogen hormone, interacting with ESR1/2 receptors, is an essential sex factor that protects COVID-19 patients by inhibiting inflammation and immune response caused by SARS-CoV-2 infection. Medications perturb the down-stream of ESR1/ESR2 to inhibit the inflammation and immune response can be effective or synergistic combined with other existing drugs for COVID-19 treatment. American Journal Experts 2021-09-30 /pmc/articles/PMC8491851/ /pubmed/34611658 http://dx.doi.org/10.21203/rs.3.rs-936900/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Li, Fuhai
Boon, Adrianus C.M.
Michelson, Andrew P.
Foraker, Randi E.
Zhan, Ming
Payne, Philip R.O.
Estrogen hormone is an essential sex factor inhibiting inflammation and immune response in COVID-19
title Estrogen hormone is an essential sex factor inhibiting inflammation and immune response in COVID-19
title_full Estrogen hormone is an essential sex factor inhibiting inflammation and immune response in COVID-19
title_fullStr Estrogen hormone is an essential sex factor inhibiting inflammation and immune response in COVID-19
title_full_unstemmed Estrogen hormone is an essential sex factor inhibiting inflammation and immune response in COVID-19
title_short Estrogen hormone is an essential sex factor inhibiting inflammation and immune response in COVID-19
title_sort estrogen hormone is an essential sex factor inhibiting inflammation and immune response in covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491851/
https://www.ncbi.nlm.nih.gov/pubmed/34611658
http://dx.doi.org/10.21203/rs.3.rs-936900/v1
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