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Dendritic cell cross‐dressing and tumor immunity

In addition to direct and cross‐presentation, dendritic cells (DCs) can present tumor antigens (TAs) to T cells via a hitherto poorly understood mechanism called “cross‐dressing.” DC cross‐dressing involves the acquisition of preformed peptide‐major histocompatibility class I/II (p‐MHC) complexes fr...

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Detalles Bibliográficos
Autores principales: Martinez‐Usatorre, Amaia, De Palma, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549722/
https://www.ncbi.nlm.nih.gov/pubmed/35959554
http://dx.doi.org/10.15252/emmm.202216523
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author Martinez‐Usatorre, Amaia
De Palma, Michele
author_facet Martinez‐Usatorre, Amaia
De Palma, Michele
author_sort Martinez‐Usatorre, Amaia
collection PubMed
description In addition to direct and cross‐presentation, dendritic cells (DCs) can present tumor antigens (TAs) to T cells via a hitherto poorly understood mechanism called “cross‐dressing.” DC cross‐dressing involves the acquisition of preformed peptide‐major histocompatibility class I/II (p‐MHC) complexes from cancer cells. This process has been documented both in cell culture and in tumor models; may occur via the uptake of tumor‐derived extracellular vesicles or the horizontal transfer of plasma membrane fragments from cancer cells to DCs; and can be enhanced through DC engineering for therapeutic applications. In some experimental contexts, DC cross‐dressing may be essential for productive anti‐tumor immunity, possibly owing to the fact that tumor‐derived p‐MHC complexes encompass the full repertoire of immunologically relevant TAs against which primed cytotoxic T cells can exert their tumoricidal activity.
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spelling pubmed-95497222022-10-14 Dendritic cell cross‐dressing and tumor immunity Martinez‐Usatorre, Amaia De Palma, Michele EMBO Mol Med Commentary In addition to direct and cross‐presentation, dendritic cells (DCs) can present tumor antigens (TAs) to T cells via a hitherto poorly understood mechanism called “cross‐dressing.” DC cross‐dressing involves the acquisition of preformed peptide‐major histocompatibility class I/II (p‐MHC) complexes from cancer cells. This process has been documented both in cell culture and in tumor models; may occur via the uptake of tumor‐derived extracellular vesicles or the horizontal transfer of plasma membrane fragments from cancer cells to DCs; and can be enhanced through DC engineering for therapeutic applications. In some experimental contexts, DC cross‐dressing may be essential for productive anti‐tumor immunity, possibly owing to the fact that tumor‐derived p‐MHC complexes encompass the full repertoire of immunologically relevant TAs against which primed cytotoxic T cells can exert their tumoricidal activity. John Wiley and Sons Inc. 2022-08-12 /pmc/articles/PMC9549722/ /pubmed/35959554 http://dx.doi.org/10.15252/emmm.202216523 Text en © 2022 The Authors. Published under the terms of the CC BY 4.0 license. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Martinez‐Usatorre, Amaia
De Palma, Michele
Dendritic cell cross‐dressing and tumor immunity
title Dendritic cell cross‐dressing and tumor immunity
title_full Dendritic cell cross‐dressing and tumor immunity
title_fullStr Dendritic cell cross‐dressing and tumor immunity
title_full_unstemmed Dendritic cell cross‐dressing and tumor immunity
title_short Dendritic cell cross‐dressing and tumor immunity
title_sort dendritic cell cross‐dressing and tumor immunity
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9549722/
https://www.ncbi.nlm.nih.gov/pubmed/35959554
http://dx.doi.org/10.15252/emmm.202216523
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