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A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines

Since the outbreak of the novel coronavirus disease 2019 (COVID-19) in Wuhan, China, many health care systems have been heavily engaged in treating and preventing the disease, and the year 2020 may be called as “historic COVID-19 vaccine breakthrough”. Due to the COVID-19 pandemic, many companies ha...

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Autores principales: Abdolmaleki, Gelareh, Taheri, Mina Azam, Paridehpour, Sarina, Mohammadi, Neshaut Mashreghi, Tabatabaei, Yasaman Ahmadi, Mousavi, Taraneh, Amin, Mohsen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436716/
https://www.ncbi.nlm.nih.gov/pubmed/36050585
http://dx.doi.org/10.1007/s40199-022-00446-8
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author Abdolmaleki, Gelareh
Taheri, Mina Azam
Paridehpour, Sarina
Mohammadi, Neshaut Mashreghi
Tabatabaei, Yasaman Ahmadi
Mousavi, Taraneh
Amin, Mohsen
author_facet Abdolmaleki, Gelareh
Taheri, Mina Azam
Paridehpour, Sarina
Mohammadi, Neshaut Mashreghi
Tabatabaei, Yasaman Ahmadi
Mousavi, Taraneh
Amin, Mohsen
author_sort Abdolmaleki, Gelareh
collection PubMed
description Since the outbreak of the novel coronavirus disease 2019 (COVID-19) in Wuhan, China, many health care systems have been heavily engaged in treating and preventing the disease, and the year 2020 may be called as “historic COVID-19 vaccine breakthrough”. Due to the COVID-19 pandemic, many companies have initiated investigations on developing an efficient and safe vaccine against the virus. From Moderna and Pfizer in the United States to PastocoVac in Pasteur Institute of Iran and the University of Oxford in the United Kingdom, different candidates have been introduced to the market. COVID-19 vaccine research has been facilitated based on genome and structural information, bioinformatics predictions, epitope mapping, and data obtained from the previous developments of severe acute respiratory syndrome coronavirus (SARS-CoV or SARS-CoV-1) and middle east respiratory syndrome coronavirus (MERS-CoV) vaccine candidates. SARS-CoV genome sequence is highly homologous to the one in COVID-19 and both viruses use the same receptor, angiotensin-converting enzyme 2 (ACE2). Moreover, the immune system responds to these viruses, partially in the same way. Considering the on-going COVID-19 pandemic and previous attempts to manufacture SARS-CoV vaccines, this paper is going to discuss clinical cases as well as vaccine challenges, including those related to infrastructures, transportation, possible adverse reactions, utilized delivery systems (e.g., nanotechnology and electroporation) and probable vaccine-induced mutations. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-94367162022-09-02 A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines Abdolmaleki, Gelareh Taheri, Mina Azam Paridehpour, Sarina Mohammadi, Neshaut Mashreghi Tabatabaei, Yasaman Ahmadi Mousavi, Taraneh Amin, Mohsen Daru Review Article Since the outbreak of the novel coronavirus disease 2019 (COVID-19) in Wuhan, China, many health care systems have been heavily engaged in treating and preventing the disease, and the year 2020 may be called as “historic COVID-19 vaccine breakthrough”. Due to the COVID-19 pandemic, many companies have initiated investigations on developing an efficient and safe vaccine against the virus. From Moderna and Pfizer in the United States to PastocoVac in Pasteur Institute of Iran and the University of Oxford in the United Kingdom, different candidates have been introduced to the market. COVID-19 vaccine research has been facilitated based on genome and structural information, bioinformatics predictions, epitope mapping, and data obtained from the previous developments of severe acute respiratory syndrome coronavirus (SARS-CoV or SARS-CoV-1) and middle east respiratory syndrome coronavirus (MERS-CoV) vaccine candidates. SARS-CoV genome sequence is highly homologous to the one in COVID-19 and both viruses use the same receptor, angiotensin-converting enzyme 2 (ACE2). Moreover, the immune system responds to these viruses, partially in the same way. Considering the on-going COVID-19 pandemic and previous attempts to manufacture SARS-CoV vaccines, this paper is going to discuss clinical cases as well as vaccine challenges, including those related to infrastructures, transportation, possible adverse reactions, utilized delivery systems (e.g., nanotechnology and electroporation) and probable vaccine-induced mutations. GRAPHICAL ABSTRACT: [Image: see text] Springer International Publishing 2022-09-02 /pmc/articles/PMC9436716/ /pubmed/36050585 http://dx.doi.org/10.1007/s40199-022-00446-8 Text en © The Author(s), under exclusive licence to Tehran University of Medical Sciences 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
spellingShingle Review Article
Abdolmaleki, Gelareh
Taheri, Mina Azam
Paridehpour, Sarina
Mohammadi, Neshaut Mashreghi
Tabatabaei, Yasaman Ahmadi
Mousavi, Taraneh
Amin, Mohsen
A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines
title A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines
title_full A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines
title_fullStr A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines
title_full_unstemmed A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines
title_short A comparison between SARS-CoV-1 and SARS-CoV2: an update on current COVID-19 vaccines
title_sort comparison between sars-cov-1 and sars-cov2: an update on current covid-19 vaccines
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9436716/
https://www.ncbi.nlm.nih.gov/pubmed/36050585
http://dx.doi.org/10.1007/s40199-022-00446-8
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