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T Cell Epitope Discovery in the Context of Distinct and Unique Indigenous HLA Profiles
CD8(+) T cells are a pivotal part of the immune response to viruses, playing a key role in disease outcome and providing long-lasting immunity to conserved pathogen epitopes. Understanding CD8(+) T cell immunity in humans is complex due to CD8(+) T cell restriction by highly polymorphic Human Leukoc...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121770/ https://www.ncbi.nlm.nih.gov/pubmed/35603215 http://dx.doi.org/10.3389/fimmu.2022.812393 |
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author | Hensen, Luca Illing, Patricia T. Rowntree, Louise C. Davies, Jane Miller, Adrian Tong, Steven Y. C. Habel, Jennifer R. van de Sandt, Carolien E. Flanagan, Katie L. Purcell, Anthony W. Kedzierska, Katherine Clemens, E. Bridie |
author_facet | Hensen, Luca Illing, Patricia T. Rowntree, Louise C. Davies, Jane Miller, Adrian Tong, Steven Y. C. Habel, Jennifer R. van de Sandt, Carolien E. Flanagan, Katie L. Purcell, Anthony W. Kedzierska, Katherine Clemens, E. Bridie |
author_sort | Hensen, Luca |
collection | PubMed |
description | CD8(+) T cells are a pivotal part of the immune response to viruses, playing a key role in disease outcome and providing long-lasting immunity to conserved pathogen epitopes. Understanding CD8(+) T cell immunity in humans is complex due to CD8(+) T cell restriction by highly polymorphic Human Leukocyte Antigen (HLA) proteins, requiring T cell epitopes to be defined for different HLA allotypes across different ethnicities. Here we evaluate strategies that have been developed to facilitate epitope identification and study immunogenic T cell responses. We describe an immunopeptidomics approach to sequence HLA-bound peptides presented on virus-infected cells by liquid chromatography with tandem mass spectrometry (LC-MS/MS). Using antigen presenting cell lines that stably express the HLA alleles characteristic of Indigenous Australians, this approach has been successfully used to comprehensively identify influenza-specific CD8(+) T cell epitopes restricted by HLA allotypes predominant in Indigenous Australians, including HLA-A*24:02 and HLA-A*11:01. This is an essential step in ensuring high vaccine coverage and efficacy in Indigenous populations globally, known to be at high risk from influenza disease and other respiratory infections. |
format | Online Article Text |
id | pubmed-9121770 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91217702022-05-21 T Cell Epitope Discovery in the Context of Distinct and Unique Indigenous HLA Profiles Hensen, Luca Illing, Patricia T. Rowntree, Louise C. Davies, Jane Miller, Adrian Tong, Steven Y. C. Habel, Jennifer R. van de Sandt, Carolien E. Flanagan, Katie L. Purcell, Anthony W. Kedzierska, Katherine Clemens, E. Bridie Front Immunol Immunology CD8(+) T cells are a pivotal part of the immune response to viruses, playing a key role in disease outcome and providing long-lasting immunity to conserved pathogen epitopes. Understanding CD8(+) T cell immunity in humans is complex due to CD8(+) T cell restriction by highly polymorphic Human Leukocyte Antigen (HLA) proteins, requiring T cell epitopes to be defined for different HLA allotypes across different ethnicities. Here we evaluate strategies that have been developed to facilitate epitope identification and study immunogenic T cell responses. We describe an immunopeptidomics approach to sequence HLA-bound peptides presented on virus-infected cells by liquid chromatography with tandem mass spectrometry (LC-MS/MS). Using antigen presenting cell lines that stably express the HLA alleles characteristic of Indigenous Australians, this approach has been successfully used to comprehensively identify influenza-specific CD8(+) T cell epitopes restricted by HLA allotypes predominant in Indigenous Australians, including HLA-A*24:02 and HLA-A*11:01. This is an essential step in ensuring high vaccine coverage and efficacy in Indigenous populations globally, known to be at high risk from influenza disease and other respiratory infections. Frontiers Media S.A. 2022-05-06 /pmc/articles/PMC9121770/ /pubmed/35603215 http://dx.doi.org/10.3389/fimmu.2022.812393 Text en Copyright © 2022 Hensen, Illing, Rowntree, Davies, Miller, Tong, Habel, van de Sandt, Flanagan, Purcell, Kedzierska and Clemens https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Hensen, Luca Illing, Patricia T. Rowntree, Louise C. Davies, Jane Miller, Adrian Tong, Steven Y. C. Habel, Jennifer R. van de Sandt, Carolien E. Flanagan, Katie L. Purcell, Anthony W. Kedzierska, Katherine Clemens, E. Bridie T Cell Epitope Discovery in the Context of Distinct and Unique Indigenous HLA Profiles |
title | T Cell Epitope Discovery in the Context of Distinct and Unique Indigenous HLA Profiles |
title_full | T Cell Epitope Discovery in the Context of Distinct and Unique Indigenous HLA Profiles |
title_fullStr | T Cell Epitope Discovery in the Context of Distinct and Unique Indigenous HLA Profiles |
title_full_unstemmed | T Cell Epitope Discovery in the Context of Distinct and Unique Indigenous HLA Profiles |
title_short | T Cell Epitope Discovery in the Context of Distinct and Unique Indigenous HLA Profiles |
title_sort | t cell epitope discovery in the context of distinct and unique indigenous hla profiles |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9121770/ https://www.ncbi.nlm.nih.gov/pubmed/35603215 http://dx.doi.org/10.3389/fimmu.2022.812393 |
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