Preliminary Identification of Potential Vaccine Targets for the COVID-19 Coronavirus (SARS-CoV-2) Based on SARS-CoV Immunological Studies
The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain ins...
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Published in | Viruses Vol. 12; no. 3; p. 254 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
MDPI
25.02.2020
MDPI AG |
Subjects | |
Online Access | Get full text |
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Abstract | The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain insights for vaccine design against SARS-CoV-2 by considering the high genetic similarity between SARS-CoV-2 and SARS-CoV, which caused the outbreak in 2003, and leveraging existing immunological studies of SARS-CoV. By screening the experimentally-determined SARS-CoV-derived B cell and T cell epitopes in the immunogenic structural proteins of SARS-CoV, we identified a set of B cell and T cell epitopes derived from the spike (S) and nucleocapsid (N) proteins that map identically to SARS-CoV-2 proteins. As no mutation has been observed in these identified epitopes among the 120 available SARS-CoV-2 sequences (as of 21 February 2020), immune targeting of these epitopes may potentially offer protection against this novel virus. For the T cell epitopes, we performed a population coverage analysis of the associated MHC alleles and proposed a set of epitopes that is estimated to provide broad coverage globally, as well as in China. Our findings provide a screened set of epitopes that can help guide experimental efforts towards the development of vaccines against SARS-CoV-2. |
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AbstractList | The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain insights for vaccine design against SARS-CoV-2 by considering the high genetic similarity between SARS-CoV-2 and SARS-CoV, which caused the outbreak in 2003, and leveraging existing immunological studies of SARS-CoV. By screening the experimentally-determined SARS-CoV-derived B cell and T cell epitopes in the immunogenic structural proteins of SARS-CoV, we identified a set of B cell and T cell epitopes derived from the spike (S) and nucleocapsid (N) proteins that map identically to SARS-CoV-2 proteins. As no mutation has been observed in these identified epitopes among the 120 available SARS-CoV-2 sequences (as of 21 February 2020), immune targeting of these epitopes may potentially offer protection against this novel virus. For the T cell epitopes, we performed a population coverage analysis of the associated MHC alleles and proposed a set of epitopes that is estimated to provide broad coverage globally, as well as in China. Our findings provide a screened set of epitopes that can help guide experimental efforts towards the development of vaccines against SARS-CoV-2.The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain insights for vaccine design against SARS-CoV-2 by considering the high genetic similarity between SARS-CoV-2 and SARS-CoV, which caused the outbreak in 2003, and leveraging existing immunological studies of SARS-CoV. By screening the experimentally-determined SARS-CoV-derived B cell and T cell epitopes in the immunogenic structural proteins of SARS-CoV, we identified a set of B cell and T cell epitopes derived from the spike (S) and nucleocapsid (N) proteins that map identically to SARS-CoV-2 proteins. As no mutation has been observed in these identified epitopes among the 120 available SARS-CoV-2 sequences (as of 21 February 2020), immune targeting of these epitopes may potentially offer protection against this novel virus. For the T cell epitopes, we performed a population coverage analysis of the associated MHC alleles and proposed a set of epitopes that is estimated to provide broad coverage globally, as well as in China. Our findings provide a screened set of epitopes that can help guide experimental efforts towards the development of vaccines against SARS-CoV-2. The beginning of 2020 has seen the emergence of COVID-19 outbreak caused by a novel coronavirus, Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2). There is an imminent need to better understand this new virus and to develop ways to control its spread. In this study, we sought to gain insights for vaccine design against SARS-CoV-2 by considering the high genetic similarity between SARS-CoV-2 and SARS-CoV, which caused the outbreak in 2003, and leveraging existing immunological studies of SARS-CoV. By screening the experimentally-determined SARS-CoV-derived B cell and T cell epitopes in the immunogenic structural proteins of SARS-CoV, we identified a set of B cell and T cell epitopes derived from the spike (S) and nucleocapsid (N) proteins that map identically to SARS-CoV-2 proteins. As no mutation has been observed in these identified epitopes among the 120 available SARS-CoV-2 sequences (as of 21 February 2020), immune targeting of these epitopes may potentially offer protection against this novel virus. For the T cell epitopes, we performed a population coverage analysis of the associated MHC alleles and proposed a set of epitopes that is estimated to provide broad coverage globally, as well as in China. Our findings provide a screened set of epitopes that can help guide experimental efforts towards the development of vaccines against SARS-CoV-2. |
Author | Ahmed, Syed Faraz Quadeer, Ahmed A. McKay, Matthew R. |
AuthorAffiliation | 1 Department of Electronic and Computer Engineering, The Hong Kong University of Science and Technology, Hong Kong, China; sfahmed@connect.ust.hk 2 Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong, China |
AuthorAffiliation_xml | – name: 2 Department of Chemical and Biological Engineering, The Hong Kong University of Science and Technology, Hong Kong, China – name: 1 Department of Electronic and Computer Engineering, The Hong Kong University of Science and Technology, Hong Kong, China; sfahmed@connect.ust.hk |
Author_xml | – sequence: 1 givenname: Syed Faraz orcidid: 0000-0002-6086-0307 surname: Ahmed fullname: Ahmed, Syed Faraz – sequence: 2 givenname: Ahmed A. orcidid: 0000-0002-5295-9067 surname: Quadeer fullname: Quadeer, Ahmed A. – sequence: 3 givenname: Matthew R. surname: McKay fullname: McKay, Matthew R. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32106567$$D View this record in MEDLINE/PubMed |
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Keywords | B cell epitopes COVID-19 SARS-CoV-2 vaccine Coronavirus T cell epitopes 2019 novel coronavirus SARS-CoV MERS-CoV 2019-nCoV |
Language | English |
License | https://creativecommons.org/licenses/by/4.0 Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
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SubjectTerms | 2019 novel coronavirus 2019-ncov b cell epitopes Betacoronavirus - genetics Betacoronavirus - immunology coronavirus Coronavirus Infections - prevention & control Coronavirus Nucleocapsid Proteins COVID-19 COVID-19 Vaccines Epitope Mapping Epitopes, B-Lymphocyte - genetics Epitopes, B-Lymphocyte - immunology Epitopes, T-Lymphocyte - genetics Epitopes, T-Lymphocyte - immunology Genome, Viral Humans mers-cov Nucleocapsid Proteins - genetics Nucleocapsid Proteins - immunology Phosphoproteins Phylogeny Pneumonia, Viral - prevention & control Protein Structure, Tertiary sars-cov SARS-CoV-2 Severe acute respiratory syndrome-related coronavirus - genetics Severe acute respiratory syndrome-related coronavirus - immunology Spike Glycoprotein, Coronavirus - genetics Spike Glycoprotein, Coronavirus - immunology t cell epitopes vaccine Viral Vaccines - immunology |
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