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Vitamin A in resistance to and recovery from infection: relevance to SARS-CoV2

SARS-CoV2 infects respiratory epithelial cells via its cellular receptor angiotensin-converting enzyme 2, causing a viral pneumonia with pronounced inflammation resulting in significant damage to the lungs and other organ systems, including the kidneys, though symptoms and disease severity are quite...

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Autores principales: Stephensen, C. B., Lietz, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884725/
https://www.ncbi.nlm.nih.gov/pubmed/33468263
http://dx.doi.org/10.1017/S0007114521000246
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author Stephensen, C. B.
Lietz, G.
author_facet Stephensen, C. B.
Lietz, G.
author_sort Stephensen, C. B.
collection PubMed
description SARS-CoV2 infects respiratory epithelial cells via its cellular receptor angiotensin-converting enzyme 2, causing a viral pneumonia with pronounced inflammation resulting in significant damage to the lungs and other organ systems, including the kidneys, though symptoms and disease severity are quite variable depending on the intensity of exposure and presence of underlying conditions that may affect the immune response. The resulting disease, coronavirus disease 2019 (COVID-19), can cause multi-organ system dysfunction in patients requiring hospitalisation and intensive care treatment. Serious infections like COVID-19 often negatively affect nutritional status, and the resulting nutritional deficiencies may increase disease severity and impair recovery. One example is the viral infection measles, where associated vitamin A (VA) deficiency increases disease severity and appropriately timed supplementation during recovery reduces mortality and hastens recovery. VA may play a similar role in COVID-19. First, VA is important in maintaining innate and adaptive immunity to promote clearance of a primary infection as well as minimise risks from secondary infections. Second, VA plays a unique role in the respiratory tract, minimising damaging inflammation, supporting repair of respiratory epithelium and preventing fibrosis. Third, VA deficiency may develop during COVID-19 due to specific effects on lung and liver stores caused by inflammation and impaired kidney function, suggesting that supplements may be needed to restore adequate status. Fourth, VA supplementation may counteract adverse effects of SARS-CoV2 on the angiotensin system as well as minimises adverse effects of some COVID-19 therapies. Evaluating interactions of SARS-CoV2 infection with VA metabolism may thus provide improved COVID-19 therapy.
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spelling pubmed-78847252021-02-16 Vitamin A in resistance to and recovery from infection: relevance to SARS-CoV2 Stephensen, C. B. Lietz, G. Br J Nutr Systematic Review and Meta-Analysis SARS-CoV2 infects respiratory epithelial cells via its cellular receptor angiotensin-converting enzyme 2, causing a viral pneumonia with pronounced inflammation resulting in significant damage to the lungs and other organ systems, including the kidneys, though symptoms and disease severity are quite variable depending on the intensity of exposure and presence of underlying conditions that may affect the immune response. The resulting disease, coronavirus disease 2019 (COVID-19), can cause multi-organ system dysfunction in patients requiring hospitalisation and intensive care treatment. Serious infections like COVID-19 often negatively affect nutritional status, and the resulting nutritional deficiencies may increase disease severity and impair recovery. One example is the viral infection measles, where associated vitamin A (VA) deficiency increases disease severity and appropriately timed supplementation during recovery reduces mortality and hastens recovery. VA may play a similar role in COVID-19. First, VA is important in maintaining innate and adaptive immunity to promote clearance of a primary infection as well as minimise risks from secondary infections. Second, VA plays a unique role in the respiratory tract, minimising damaging inflammation, supporting repair of respiratory epithelium and preventing fibrosis. Third, VA deficiency may develop during COVID-19 due to specific effects on lung and liver stores caused by inflammation and impaired kidney function, suggesting that supplements may be needed to restore adequate status. Fourth, VA supplementation may counteract adverse effects of SARS-CoV2 on the angiotensin system as well as minimises adverse effects of some COVID-19 therapies. Evaluating interactions of SARS-CoV2 infection with VA metabolism may thus provide improved COVID-19 therapy. Cambridge University Press 2021-01-20 /pmc/articles/PMC7884725/ /pubmed/33468263 http://dx.doi.org/10.1017/S0007114521000246 Text en © The Author(s) 2021 http://creativecommons.org/licenses/by/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Systematic Review and Meta-Analysis
Stephensen, C. B.
Lietz, G.
Vitamin A in resistance to and recovery from infection: relevance to SARS-CoV2
title Vitamin A in resistance to and recovery from infection: relevance to SARS-CoV2
title_full Vitamin A in resistance to and recovery from infection: relevance to SARS-CoV2
title_fullStr Vitamin A in resistance to and recovery from infection: relevance to SARS-CoV2
title_full_unstemmed Vitamin A in resistance to and recovery from infection: relevance to SARS-CoV2
title_short Vitamin A in resistance to and recovery from infection: relevance to SARS-CoV2
title_sort vitamin a in resistance to and recovery from infection: relevance to sars-cov2
topic Systematic Review and Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7884725/
https://www.ncbi.nlm.nih.gov/pubmed/33468263
http://dx.doi.org/10.1017/S0007114521000246
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