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

Nat Commun. 2023 May 30;14(1):3106. doi: 10.1038/s41467-023-38703-2.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Blood-Brain Barrier* / metabolism
  • CD8-Positive T-Lymphocytes
  • Central Nervous System / metabolism
  • Endothelial Cells / metabolism
  • Histocompatibility Antigens Class I / metabolism
  • Humans
  • Multiple Sclerosis*

Substances

  • Histocompatibility Antigens Class I