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...
Guardado en:
Autores principales: | , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
American Society for Microbiology
2021
|
Materias: | |
Acceso en línea: | https://doaj.org/article/933d0ab64c25497f97fe5f6157b51f9f |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:933d0ab64c25497f97fe5f6157b51f9f |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:933d0ab64c25497f97fe5f6157b51f9f2021-12-02T19:42:55ZLeveraging Immunopeptidomics To Study and Combat Infectious Disease2379-507710.1128/mSystems.00310-21https://doaj.org/article/933d0ab64c25497f97fe5f6157b51f9f2021-08-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSystems.00310-21https://doaj.org/toc/2379-5077 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.Owen K. LeddyForest M. WhiteBryan D. BrysonAmerican Society for MicrobiologyarticleMicrobiologyQR1-502ENmSystems, Vol 6, Iss 4 (2021) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Microbiology QR1-502 |
spellingShingle |
Microbiology QR1-502 Owen K. Leddy Forest M. White Bryan D. Bryson Leveraging Immunopeptidomics To Study and Combat Infectious Disease |
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. |
format |
article |
author |
Owen K. Leddy Forest M. White Bryan D. Bryson |
author_facet |
Owen K. Leddy Forest M. White Bryan D. Bryson |
author_sort |
Owen K. Leddy |
title |
Leveraging Immunopeptidomics To Study and Combat Infectious Disease |
title_short |
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_sort |
leveraging immunopeptidomics to study and combat infectious disease |
publisher |
American Society for Microbiology |
publishDate |
2021 |
url |
https://doaj.org/article/933d0ab64c25497f97fe5f6157b51f9f |
work_keys_str_mv |
AT owenkleddy leveragingimmunopeptidomicstostudyandcombatinfectiousdisease AT forestmwhite leveragingimmunopeptidomicstostudyandcombatinfectiousdisease AT bryandbryson leveragingimmunopeptidomicstostudyandcombatinfectiousdisease |
_version_ |
1718376097588969472 |