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Antigen Presentation by MHC-Dressed Cells

Professional antigen-presenting cells (APCs) such as conventional dendritic cells (DCs) process protein antigens to MHC-bound peptides and then present the peptide–MHC complexes to T cells. In addition to this canonical antigen presentation pathway, recent studies have revealed that DCs and non-APCs...

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Autor principal: Nakayama, Masafumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283639/
https://www.ncbi.nlm.nih.gov/pubmed/25601867
http://dx.doi.org/10.3389/fimmu.2014.00672
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author Nakayama, Masafumi
author_facet Nakayama, Masafumi
author_sort Nakayama, Masafumi
collection PubMed
description Professional antigen-presenting cells (APCs) such as conventional dendritic cells (DCs) process protein antigens to MHC-bound peptides and then present the peptide–MHC complexes to T cells. In addition to this canonical antigen presentation pathway, recent studies have revealed that DCs and non-APCs can acquire MHC class I (MHCI) and/or MHC class II (MHCII) from neighboring cells through a process of cell–cell contact-dependent membrane transfer called trogocytosis. These MHC-dressed cells subsequently activate or regulate T cells via the preformed antigen peptide–MHC complexes without requiring any further processing. In addition to trogocytosis, intercellular transfer of MHCI and MHCII can be mediated by secretion of membrane vesicles such as exosomes from APCs, generating MHC-dressed cells. This review focuses on the physiological role of antigen presentation by MHCI- or MHCII-dressed cells, and also discusses differences and similarities between trogocytosis and exosome-mediated transfer of MHC.
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spelling pubmed-42836392015-01-19 Antigen Presentation by MHC-Dressed Cells Nakayama, Masafumi Front Immunol Immunology Professional antigen-presenting cells (APCs) such as conventional dendritic cells (DCs) process protein antigens to MHC-bound peptides and then present the peptide–MHC complexes to T cells. In addition to this canonical antigen presentation pathway, recent studies have revealed that DCs and non-APCs can acquire MHC class I (MHCI) and/or MHC class II (MHCII) from neighboring cells through a process of cell–cell contact-dependent membrane transfer called trogocytosis. These MHC-dressed cells subsequently activate or regulate T cells via the preformed antigen peptide–MHC complexes without requiring any further processing. In addition to trogocytosis, intercellular transfer of MHCI and MHCII can be mediated by secretion of membrane vesicles such as exosomes from APCs, generating MHC-dressed cells. This review focuses on the physiological role of antigen presentation by MHCI- or MHCII-dressed cells, and also discusses differences and similarities between trogocytosis and exosome-mediated transfer of MHC. Frontiers Media S.A. 2015-01-05 /pmc/articles/PMC4283639/ /pubmed/25601867 http://dx.doi.org/10.3389/fimmu.2014.00672 Text en Copyright © 2015 Nakayama. http://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) or licensor 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
Nakayama, Masafumi
Antigen Presentation by MHC-Dressed Cells
title Antigen Presentation by MHC-Dressed Cells
title_full Antigen Presentation by MHC-Dressed Cells
title_fullStr Antigen Presentation by MHC-Dressed Cells
title_full_unstemmed Antigen Presentation by MHC-Dressed Cells
title_short Antigen Presentation by MHC-Dressed Cells
title_sort antigen presentation by mhc-dressed cells
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283639/
https://www.ncbi.nlm.nih.gov/pubmed/25601867
http://dx.doi.org/10.3389/fimmu.2014.00672
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