Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Jun;48(4):e12789.
doi: 10.1111/nan.12789. Epub 2022 Jan 13.

The blood-CSF-brain route of neurological disease: The indirect pathway into the brain

Affiliations
Free article
Review

The blood-CSF-brain route of neurological disease: The indirect pathway into the brain

Oliver Cousins et al. Neuropathol Appl Neurobiol. 2022 Jun.
Free article

Abstract

The brain is protected by the endothelial blood-brain barrier (BBB) that limits the access of micro-organisms, tumour cells, immune cells and autoantibodies to the parenchyma. However, the classic model of disease spread across a disrupted BBB does not explain the focal distribution of lesions seen in a variety of neurological diseases and why lesions are frequently adjacent to the cerebrospinal fluid (CSF) spaces. We have critically reviewed the possible role of a blood-CSF-brain route as a disease entry pathway into the brain parenchyma. The initial step of this pathway is the transfer of pathogens or immune components from the blood into the CSF at the choroid plexuses, where the blood-CSF barrier (BCSFB) is located. The flow of CSF results in disease dissemination throughout the CSF spaces. Access to the brain parenchyma from the CSF can then occur across the ependymal layer at the ventricular surface or across the pial-glial barrier of the subarachnoid space and the Virchow-Robin spaces. We have reviewed the anatomy and physiology of the blood-CSF-brain pathway and the brain barriers controlling this process. We then summarised the evidence supporting this brain entry route in a cross-section of neurological diseases including neuromyelitis optica, multiple sclerosis, neurosarcoidosis, neuropsychiatric lupus, cryptococcal infection and both solid and haematological tumours. This summary highlights the conditions that share the blood-CSF-brain pathway as a pathogenetic mechanism. These include the characteristic proximity of lesions to CSF, evidence of disruption of the brain barriers and the identification of significant pathology within the CSF. An improved understanding of pathological transfer through the CSF and across all brain barriers will inform on more effective and targeted treatments of primary and secondary diseases of the central nervous system.

Keywords: Virchow-Robin spaces; blood-CSF barrier; blood-brain barrier; choroid plexus.

PubMed Disclaimer

References

REFERENCES

    1. Wright BL, Lai JT, Sinclair AJ. Cerebrospinal fluid and lumbar puncture: A practical review. J Neurol. 2012;259:1530-1545.
    1. Miyan J, Cains S, Larcombe S, et al. Subarachnoid cerebrospinal fluid is essential for normal development of the cerebral cortex. Semin Cell Dev Biol. 2020;102:28-39.
    1. Spector R, Robert Snodgrass S, Johanson CE. A balanced view of the cerebrospinal fluid composition and functions: Focus on adult humans. Exp Neurol. 2015;273:57-68.
    1. Johanson CE, Duncan JA 3rd, Klinge PM, Brinker T, Stopa EG, Silverberg GD. Multiplicity of cerebrospinal fluid functions: New challenges in health and disease. Cerebrospinal Fluid Res. 2008;5(1):10.
    1. Bradbury M. Lymphatics and the central nervous system. Trends Neurosci. 1981;4:100-101.