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The T Cell Epitope Landscape of SARS-CoV-2 Variants of Concern

During the COVID-19 pandemic, several SARS-CoV-2 variants of concern (VOC) emerged, bringing with them varying degrees of health and socioeconomic burdens. In particular, the Omicron VOC displayed distinct features of increased transmissibility accompanied by antigenic drift in the spike protein tha...

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Autores principales: Tennøe, Simen, Gheorghe, Marius, Stratford, Richard, Clancy, Trevor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315645/
https://www.ncbi.nlm.nih.gov/pubmed/35891287
http://dx.doi.org/10.3390/vaccines10071123
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author Tennøe, Simen
Gheorghe, Marius
Stratford, Richard
Clancy, Trevor
author_facet Tennøe, Simen
Gheorghe, Marius
Stratford, Richard
Clancy, Trevor
author_sort Tennøe, Simen
collection PubMed
description During the COVID-19 pandemic, several SARS-CoV-2 variants of concern (VOC) emerged, bringing with them varying degrees of health and socioeconomic burdens. In particular, the Omicron VOC displayed distinct features of increased transmissibility accompanied by antigenic drift in the spike protein that partially circumvented the ability of pre-existing antibody responses in the global population to neutralize the virus. However, T cell immunity has remained robust throughout all the different VOC transmission waves and has emerged as a critically important correlate of protection against SARS-CoV-2 and its VOCs, in both vaccinated and infected individuals. Therefore, as SARS-CoV-2 VOCs continue to evolve, it is crucial that we characterize the correlates of protection and the potential for immune escape for both B cell and T cell human immunity in the population. Generating the insights necessary to understand T cell immunity, experimentally, for the global human population is at present a critical but a time consuming, expensive, and laborious process. Further, it is not feasible to generate global or universal insights into T cell immunity in an actionable time frame for potential future emerging VOCs. However, using computational means we can expedite and provide early insights into the correlates of T cell protection. In this study, we generated and revealed insights on the T cell epitope landscape for the five main SARS-CoV-2 VOCs observed to date. We demonstrated using a unique AI prediction platform, a significant conservation of presentable T cell epitopes across all mutated peptides for each VOC. This was modeled using the most frequent HLA alleles in the human population and covers the most common HLA haplotypes in the human population. The AI resource generated through this computational study and associated insights may guide the development of T cell vaccines and diagnostics that are even more robust against current and future VOCs, and their emerging subvariants.
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spelling pubmed-93156452022-07-27 The T Cell Epitope Landscape of SARS-CoV-2 Variants of Concern Tennøe, Simen Gheorghe, Marius Stratford, Richard Clancy, Trevor Vaccines (Basel) Article During the COVID-19 pandemic, several SARS-CoV-2 variants of concern (VOC) emerged, bringing with them varying degrees of health and socioeconomic burdens. In particular, the Omicron VOC displayed distinct features of increased transmissibility accompanied by antigenic drift in the spike protein that partially circumvented the ability of pre-existing antibody responses in the global population to neutralize the virus. However, T cell immunity has remained robust throughout all the different VOC transmission waves and has emerged as a critically important correlate of protection against SARS-CoV-2 and its VOCs, in both vaccinated and infected individuals. Therefore, as SARS-CoV-2 VOCs continue to evolve, it is crucial that we characterize the correlates of protection and the potential for immune escape for both B cell and T cell human immunity in the population. Generating the insights necessary to understand T cell immunity, experimentally, for the global human population is at present a critical but a time consuming, expensive, and laborious process. Further, it is not feasible to generate global or universal insights into T cell immunity in an actionable time frame for potential future emerging VOCs. However, using computational means we can expedite and provide early insights into the correlates of T cell protection. In this study, we generated and revealed insights on the T cell epitope landscape for the five main SARS-CoV-2 VOCs observed to date. We demonstrated using a unique AI prediction platform, a significant conservation of presentable T cell epitopes across all mutated peptides for each VOC. This was modeled using the most frequent HLA alleles in the human population and covers the most common HLA haplotypes in the human population. The AI resource generated through this computational study and associated insights may guide the development of T cell vaccines and diagnostics that are even more robust against current and future VOCs, and their emerging subvariants. MDPI 2022-07-14 /pmc/articles/PMC9315645/ /pubmed/35891287 http://dx.doi.org/10.3390/vaccines10071123 Text en © 2022 by the authors. 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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tennøe, Simen
Gheorghe, Marius
Stratford, Richard
Clancy, Trevor
The T Cell Epitope Landscape of SARS-CoV-2 Variants of Concern
title The T Cell Epitope Landscape of SARS-CoV-2 Variants of Concern
title_full The T Cell Epitope Landscape of SARS-CoV-2 Variants of Concern
title_fullStr The T Cell Epitope Landscape of SARS-CoV-2 Variants of Concern
title_full_unstemmed The T Cell Epitope Landscape of SARS-CoV-2 Variants of Concern
title_short The T Cell Epitope Landscape of SARS-CoV-2 Variants of Concern
title_sort t cell epitope landscape of sars-cov-2 variants of concern
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315645/
https://www.ncbi.nlm.nih.gov/pubmed/35891287
http://dx.doi.org/10.3390/vaccines10071123
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