Emergence of the brain-border immune niches and their contribution to the development of neurodegenerative diseases

Front Immunol. 2024 May 28:15:1380063. doi: 10.3389/fimmu.2024.1380063. eCollection 2024.

Abstract

Historically, the central nervous system (CNS) was regarded as 'immune-privileged', possessing its own distinct immune cell population. This immune privilege was thought to be established by a tight blood-brain barrier (BBB) and blood-cerebrospinal-fluid barrier (BCSFB), which prevented the crossing of peripheral immune cells and their secreted factors into the CNS parenchyma. However, recent studies have revealed the presence of peripheral immune cells in proximity to various brain-border niches such as the choroid plexus, cranial bone marrow (CBM), meninges, and perivascular spaces. Furthermore, emerging evidence suggests that peripheral immune cells may be able to infiltrate the brain through these sites and play significant roles in driving neuronal cell death and pathology progression in neurodegenerative disease. Thus, in this review, we explore how the brain-border immune niches may contribute to the pathogenesis of neurodegenerative disorders such as Alzheimer's disease (AD), Parkinson's disease (PD), and multiple sclerosis (MS). We then discuss several emerging options for harnessing the neuroimmune potential of these niches to improve the prognosis and treatment of these debilitative disorders using novel insights from recent studies.

Keywords: Alzheimer’s disease; Parkinson’s disease; brain-border; multiple sclerosis; neurodegeneration; neuroimmune.

Publication types

  • Review

MeSH terms

  • Animals
  • Blood-Brain Barrier* / immunology
  • Brain* / immunology
  • Brain* / pathology
  • Humans
  • Immune Privilege
  • Neurodegenerative Diseases* / immunology
  • Neurodegenerative Diseases* / pathology

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the industry academic cooperation foundation fund, CHA University Gr ant (CHA-202300230001).