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Leveraging Immunopeptidomics To Study and Combat Infectious Disease

T cells must recognize pathogen-derived peptides bound to major histocompatibility complexes (MHCs) in order to initiate a cell-mediated immune response against an infection, or to support the development of high-affinity antibody responses. Identifying antigens presented on MHCs by infected cells a...

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Detalles Bibliográficos
Autores principales: Leddy, Owen K., White, Forest M., Bryson, Bryan D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407116/
https://www.ncbi.nlm.nih.gov/pubmed/34342538
http://dx.doi.org/10.1128/mSystems.00310-21
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author Leddy, Owen K.
White, Forest M.
Bryson, Bryan D.
author_facet Leddy, Owen K.
White, Forest M.
Bryson, Bryan D.
author_sort Leddy, Owen K.
collection PubMed
description T cells must recognize pathogen-derived peptides bound to major histocompatibility complexes (MHCs) in order to initiate a cell-mediated immune response against an infection, or to support the development of high-affinity antibody responses. Identifying antigens presented on MHCs by infected cells and professional antigen-presenting cells (APCs) during infection may therefore provide a route toward developing new vaccines. Peptides bound to MHCs can be identified at whole-proteome scale using mass spectrometry—a technique referred to as “immunopeptidomics.” This technique has emerged as a powerful tool for identifying potential vaccine targets in the context of many infectious diseases. In this review, we discuss the contributions immunopeptidomic studies have made to understanding antigen presentation and T cell priming in the context of infection and the potential for immunopeptidomics to inform the development of vaccines to address pressing global health problems in infectious disease.
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spelling pubmed-84071162021-09-09 Leveraging Immunopeptidomics To Study and Combat Infectious Disease Leddy, Owen K. White, Forest M. Bryson, Bryan D. mSystems Minireview T cells must recognize pathogen-derived peptides bound to major histocompatibility complexes (MHCs) in order to initiate a cell-mediated immune response against an infection, or to support the development of high-affinity antibody responses. Identifying antigens presented on MHCs by infected cells and professional antigen-presenting cells (APCs) during infection may therefore provide a route toward developing new vaccines. Peptides bound to MHCs can be identified at whole-proteome scale using mass spectrometry—a technique referred to as “immunopeptidomics.” This technique has emerged as a powerful tool for identifying potential vaccine targets in the context of many infectious diseases. In this review, we discuss the contributions immunopeptidomic studies have made to understanding antigen presentation and T cell priming in the context of infection and the potential for immunopeptidomics to inform the development of vaccines to address pressing global health problems in infectious disease. American Society for Microbiology 2021-08-03 /pmc/articles/PMC8407116/ /pubmed/34342538 http://dx.doi.org/10.1128/mSystems.00310-21 Text en Copyright © 2021 Leddy et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Minireview
Leddy, Owen K.
White, Forest M.
Bryson, Bryan D.
Leveraging Immunopeptidomics To Study and Combat Infectious Disease
title Leveraging Immunopeptidomics To Study and Combat Infectious Disease
title_full Leveraging Immunopeptidomics To Study and Combat Infectious Disease
title_fullStr Leveraging Immunopeptidomics To Study and Combat Infectious Disease
title_full_unstemmed Leveraging Immunopeptidomics To Study and Combat Infectious Disease
title_short Leveraging Immunopeptidomics To Study and Combat Infectious Disease
title_sort leveraging immunopeptidomics to study and combat infectious disease
topic Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8407116/
https://www.ncbi.nlm.nih.gov/pubmed/34342538
http://dx.doi.org/10.1128/mSystems.00310-21
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