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Glycome dynamics in T and B cell development: basic immunological mechanisms and clinical applications

Glycans cover the surfaces of all mammalian cells through a process called glycosylation. Nearly all proteins and receptors that integrate the intricate series of co-stimulatory/inhibitory pathways of the immune system are glycosylated. Growing evidence indicates that the development of the immune s...

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Autores principales: Vicente, Manuel M., Leite-Gomes, Eduarda, Pinho, Salomé S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394430/
https://www.ncbi.nlm.nih.gov/pubmed/37407365
http://dx.doi.org/10.1016/j.it.2023.06.004
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author Vicente, Manuel M.
Leite-Gomes, Eduarda
Pinho, Salomé S.
author_facet Vicente, Manuel M.
Leite-Gomes, Eduarda
Pinho, Salomé S.
author_sort Vicente, Manuel M.
collection PubMed
description Glycans cover the surfaces of all mammalian cells through a process called glycosylation. Nearly all proteins and receptors that integrate the intricate series of co-stimulatory/inhibitory pathways of the immune system are glycosylated. Growing evidence indicates that the development of the immune system at the origins of T and B cell development is tightly regulated by glycosylation. In this opinion, we hypothesize that the glycome composition of developing T and B cells is developmentally regulated. We discuss how glycans play fundamental roles in lymphocyte development and how glycans early define T and B cell functionality in multiple aspects of adaptive immunity. These advances can provide opportunities for the discovery of novel disease factors and more effective candidate treatments for various conditions.
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spelling pubmed-103944302023-08-03 Glycome dynamics in T and B cell development: basic immunological mechanisms and clinical applications Vicente, Manuel M. Leite-Gomes, Eduarda Pinho, Salomé S. Trends Immunol Opinion Glycans cover the surfaces of all mammalian cells through a process called glycosylation. Nearly all proteins and receptors that integrate the intricate series of co-stimulatory/inhibitory pathways of the immune system are glycosylated. Growing evidence indicates that the development of the immune system at the origins of T and B cell development is tightly regulated by glycosylation. In this opinion, we hypothesize that the glycome composition of developing T and B cells is developmentally regulated. We discuss how glycans play fundamental roles in lymphocyte development and how glycans early define T and B cell functionality in multiple aspects of adaptive immunity. These advances can provide opportunities for the discovery of novel disease factors and more effective candidate treatments for various conditions. Elsevier Science Ltd 2023-08 /pmc/articles/PMC10394430/ /pubmed/37407365 http://dx.doi.org/10.1016/j.it.2023.06.004 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Opinion
Vicente, Manuel M.
Leite-Gomes, Eduarda
Pinho, Salomé S.
Glycome dynamics in T and B cell development: basic immunological mechanisms and clinical applications
title Glycome dynamics in T and B cell development: basic immunological mechanisms and clinical applications
title_full Glycome dynamics in T and B cell development: basic immunological mechanisms and clinical applications
title_fullStr Glycome dynamics in T and B cell development: basic immunological mechanisms and clinical applications
title_full_unstemmed Glycome dynamics in T and B cell development: basic immunological mechanisms and clinical applications
title_short Glycome dynamics in T and B cell development: basic immunological mechanisms and clinical applications
title_sort glycome dynamics in t and b cell development: basic immunological mechanisms and clinical applications
topic Opinion
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10394430/
https://www.ncbi.nlm.nih.gov/pubmed/37407365
http://dx.doi.org/10.1016/j.it.2023.06.004
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