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Antigen recognition detains CD8(+) T cells at the blood-brain barrier and contributes to its breakdown

Blood-brain barrier (BBB) breakdown and immune cell infiltration into the central nervous system (CNS) are early hallmarks of multiple sclerosis (MS). High numbers of CD8(+) T cells are found in MS lesions, and antigen (Ag) presentation at the BBB has been proposed to promote CD8(+) T cell entry int...

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Autores principales: Aydin, Sidar, Pareja, Javier, Schallenberg, Vivianne M., Klopstein, Armelle, Gruber, Thomas, Page, Nicolas, Bouillet, Elisa, Blanchard, Nicolas, Liblau, Roland, Körbelin, Jakob, Schwaninger, Markus, Johnson, Aaron J., Schenk, Mirjam, Deutsch, Urban, Merkler, Doron, Engelhardt, Britta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229608/
https://www.ncbi.nlm.nih.gov/pubmed/37253744
http://dx.doi.org/10.1038/s41467-023-38703-2
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author Aydin, Sidar
Pareja, Javier
Schallenberg, Vivianne M.
Klopstein, Armelle
Gruber, Thomas
Page, Nicolas
Bouillet, Elisa
Blanchard, Nicolas
Liblau, Roland
Körbelin, Jakob
Schwaninger, Markus
Johnson, Aaron J.
Schenk, Mirjam
Deutsch, Urban
Merkler, Doron
Engelhardt, Britta
author_facet Aydin, Sidar
Pareja, Javier
Schallenberg, Vivianne M.
Klopstein, Armelle
Gruber, Thomas
Page, Nicolas
Bouillet, Elisa
Blanchard, Nicolas
Liblau, Roland
Körbelin, Jakob
Schwaninger, Markus
Johnson, Aaron J.
Schenk, Mirjam
Deutsch, Urban
Merkler, Doron
Engelhardt, Britta
author_sort Aydin, Sidar
collection PubMed
description Blood-brain barrier (BBB) breakdown and immune cell infiltration into the central nervous system (CNS) are early hallmarks of multiple sclerosis (MS). High numbers of CD8(+) T cells are found in MS lesions, and antigen (Ag) presentation at the BBB has been proposed to promote CD8(+) T cell entry into the CNS. Here, we show that brain endothelial cells process and cross-present Ag, leading to effector CD8(+) T cell differentiation. Under physiological flow in vitro, endothelial Ag presentation prevented CD8(+) T cell crawling and diapedesis resulting in brain endothelial cell apoptosis and BBB breakdown. Brain endothelial Ag presentation in vivo was limited due to Ag uptake by CNS-resident macrophages but still reduced motility of Ag-specific CD8(+) T cells within CNS microvessels. MHC class I-restricted Ag presentation at the BBB during neuroinflammation thus prohibits CD8(+) T cell entry into the CNS and triggers CD8(+) T cell-mediated focal BBB breakdown.
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spelling pubmed-102296082023-06-01 Antigen recognition detains CD8(+) T cells at the blood-brain barrier and contributes to its breakdown Aydin, Sidar Pareja, Javier Schallenberg, Vivianne M. Klopstein, Armelle Gruber, Thomas Page, Nicolas Bouillet, Elisa Blanchard, Nicolas Liblau, Roland Körbelin, Jakob Schwaninger, Markus Johnson, Aaron J. Schenk, Mirjam Deutsch, Urban Merkler, Doron Engelhardt, Britta Nat Commun Article Blood-brain barrier (BBB) breakdown and immune cell infiltration into the central nervous system (CNS) are early hallmarks of multiple sclerosis (MS). High numbers of CD8(+) T cells are found in MS lesions, and antigen (Ag) presentation at the BBB has been proposed to promote CD8(+) T cell entry into the CNS. Here, we show that brain endothelial cells process and cross-present Ag, leading to effector CD8(+) T cell differentiation. Under physiological flow in vitro, endothelial Ag presentation prevented CD8(+) T cell crawling and diapedesis resulting in brain endothelial cell apoptosis and BBB breakdown. Brain endothelial Ag presentation in vivo was limited due to Ag uptake by CNS-resident macrophages but still reduced motility of Ag-specific CD8(+) T cells within CNS microvessels. MHC class I-restricted Ag presentation at the BBB during neuroinflammation thus prohibits CD8(+) T cell entry into the CNS and triggers CD8(+) T cell-mediated focal BBB breakdown. Nature Publishing Group UK 2023-05-30 /pmc/articles/PMC10229608/ /pubmed/37253744 http://dx.doi.org/10.1038/s41467-023-38703-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Aydin, Sidar
Pareja, Javier
Schallenberg, Vivianne M.
Klopstein, Armelle
Gruber, Thomas
Page, Nicolas
Bouillet, Elisa
Blanchard, Nicolas
Liblau, Roland
Körbelin, Jakob
Schwaninger, Markus
Johnson, Aaron J.
Schenk, Mirjam
Deutsch, Urban
Merkler, Doron
Engelhardt, Britta
Antigen recognition detains CD8(+) T cells at the blood-brain barrier and contributes to its breakdown
title Antigen recognition detains CD8(+) T cells at the blood-brain barrier and contributes to its breakdown
title_full Antigen recognition detains CD8(+) T cells at the blood-brain barrier and contributes to its breakdown
title_fullStr Antigen recognition detains CD8(+) T cells at the blood-brain barrier and contributes to its breakdown
title_full_unstemmed Antigen recognition detains CD8(+) T cells at the blood-brain barrier and contributes to its breakdown
title_short Antigen recognition detains CD8(+) T cells at the blood-brain barrier and contributes to its breakdown
title_sort antigen recognition detains cd8(+) t cells at the blood-brain barrier and contributes to its breakdown
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229608/
https://www.ncbi.nlm.nih.gov/pubmed/37253744
http://dx.doi.org/10.1038/s41467-023-38703-2
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