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Design of a peptide-based subunit vaccine against novel coronavirus SARS-CoV-2
Coronavirus disease 2019 (COVID-19) is an emerging infectious disease that was first reported in Wuhan, China, and has subsequently spread worldwide. In the absence of any antiviral or immunomodulatory therapies, the disease is spreading at an alarming rate. A possibility of a resurgence of COVID-19...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196559/ https://www.ncbi.nlm.nih.gov/pubmed/32376359 http://dx.doi.org/10.1016/j.micpath.2020.104236 |
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author | Kalita, Parismita Padhi, Aditya K. Zhang, Kam Y.J. Tripathi, Timir |
author_facet | Kalita, Parismita Padhi, Aditya K. Zhang, Kam Y.J. Tripathi, Timir |
author_sort | Kalita, Parismita |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) is an emerging infectious disease that was first reported in Wuhan, China, and has subsequently spread worldwide. In the absence of any antiviral or immunomodulatory therapies, the disease is spreading at an alarming rate. A possibility of a resurgence of COVID-19 in places where lockdowns have already worked is also developing. Thus, for controlling COVID-19, vaccines may be a better option than drugs. An mRNA-based anti-COVID-19 candidate vaccine has entered a phase 1 clinical trial. However, its efficacy and potency have to be evaluated and validated. Since vaccines have high failure rates, as an alternative, we are presenting a new, designed multi-peptide subunit-based epitope vaccine against COVID-19. The recombinant vaccine construct comprises an adjuvant, cytotoxic T-lymphocyte (CTL), helper T-lymphocyte (HTL), and B-cell epitopes joined by linkers. The computational data suggest that the vaccine is non-toxic, non-allergenic, thermostable, with the capability to elicit a humoral and cell-mediated immune response. The stabilization of the vaccine construct is validated with molecular dynamics simulation studies. This unique vaccine is made up of 33 highly antigenic epitopes from three proteins that have a prominent role in host-receptor recognition, viral entry, and pathogenicity. We advocate this vaccine must be synthesized and tested urgently as a public health priority. |
format | Online Article Text |
id | pubmed-7196559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71965592020-05-04 Design of a peptide-based subunit vaccine against novel coronavirus SARS-CoV-2 Kalita, Parismita Padhi, Aditya K. Zhang, Kam Y.J. Tripathi, Timir Microb Pathog Article Coronavirus disease 2019 (COVID-19) is an emerging infectious disease that was first reported in Wuhan, China, and has subsequently spread worldwide. In the absence of any antiviral or immunomodulatory therapies, the disease is spreading at an alarming rate. A possibility of a resurgence of COVID-19 in places where lockdowns have already worked is also developing. Thus, for controlling COVID-19, vaccines may be a better option than drugs. An mRNA-based anti-COVID-19 candidate vaccine has entered a phase 1 clinical trial. However, its efficacy and potency have to be evaluated and validated. Since vaccines have high failure rates, as an alternative, we are presenting a new, designed multi-peptide subunit-based epitope vaccine against COVID-19. The recombinant vaccine construct comprises an adjuvant, cytotoxic T-lymphocyte (CTL), helper T-lymphocyte (HTL), and B-cell epitopes joined by linkers. The computational data suggest that the vaccine is non-toxic, non-allergenic, thermostable, with the capability to elicit a humoral and cell-mediated immune response. The stabilization of the vaccine construct is validated with molecular dynamics simulation studies. This unique vaccine is made up of 33 highly antigenic epitopes from three proteins that have a prominent role in host-receptor recognition, viral entry, and pathogenicity. We advocate this vaccine must be synthesized and tested urgently as a public health priority. Elsevier Ltd. 2020-08 2020-05-04 /pmc/articles/PMC7196559/ /pubmed/32376359 http://dx.doi.org/10.1016/j.micpath.2020.104236 Text en © 2020 Elsevier Ltd. All rights reserved. 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 Kalita, Parismita Padhi, Aditya K. Zhang, Kam Y.J. Tripathi, Timir Design of a peptide-based subunit vaccine against novel coronavirus SARS-CoV-2 |
title | Design of a peptide-based subunit vaccine against novel coronavirus SARS-CoV-2 |
title_full | Design of a peptide-based subunit vaccine against novel coronavirus SARS-CoV-2 |
title_fullStr | Design of a peptide-based subunit vaccine against novel coronavirus SARS-CoV-2 |
title_full_unstemmed | Design of a peptide-based subunit vaccine against novel coronavirus SARS-CoV-2 |
title_short | Design of a peptide-based subunit vaccine against novel coronavirus SARS-CoV-2 |
title_sort | design of a peptide-based subunit vaccine against novel coronavirus sars-cov-2 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196559/ https://www.ncbi.nlm.nih.gov/pubmed/32376359 http://dx.doi.org/10.1016/j.micpath.2020.104236 |
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