The New Spine of Access to the Brain's Secrets: Extracellular Vesicles from Cerebrospinal Fluid Liquid Biopsies in CNS Diseases and Blood-Brain Barrier Research.
I, V., Y, P., J, B., A, F., L, C., N, P., EM, I., K, O., A, G., & A, R.H. (2026). The New Spine of Access to the Brain's Secrets: Extracellular Vesicles from Cerebrospinal Fluid Liquid Biopsies in CNS Diseases and Blood-Brain Barrier Research.. Molecular neurobiology. https://doi.org/10.1007/s12035-026-06074-6
I V, Y P, J B, A F, L C, N P, et al. The New Spine of Access to the Brain's Secrets: Extracellular Vesicles from Cerebrospinal Fluid Liquid Biopsies in CNS Diseases and Blood-Brain Barrier Research.. Molecular neurobiology. 2026; doi: 10.1007/s12035-026-06074-6
I V, Y P, J B, et al. The New Spine of Access to the Brain's Secrets: Extracellular Vesicles from Cerebrospinal Fluid Liquid Biopsies in CNS Diseases and Blood-Brain Barrier Research.[J]. Molecular neurobiology. 2026. DOI: 10.1007/s12035-026-06074-6.
@article{i2026,
author = {Vermeulen I and Parmentier Y and Barber J and François A and Chadli L and Provost N and Isin EM and Ogungbenro K and Galetin A and Rostami-Hodjegan A},
title = {The New Spine of Access to the Brain's Secrets: Extracellular Vesicles from Cerebrospinal Fluid Liquid Biopsies in CNS Diseases and Blood-Brain Barrier Research.},
journal = {Molecular neurobiology},
year = {2026},
doi = {10.1007/s12035-026-06074-6},
note = {PMID: 42489808},
}
TY - JOUR AU - Vermeulen I AU - Parmentier Y AU - Barber J AU - François A AU - Chadli L AU - Provost N AU - Isin EM AU - Ogungbenro K AU - Galetin A AU - Rostami-Hodjegan A TI - The New Spine of Access to the Brain's Secrets: Extracellular Vesicles from Cerebrospinal Fluid Liquid Biopsies in CNS Diseases and Blood-Brain Barrier Research. T2 - Molecular neurobiology PY - 2026 DO - 10.1007/s12035-026-06074-6 AN - PMID:42489808 ER -
Liquid biopsy is emerging as a powerful approach for less invasive biomarker discovery, with extracellular vesicles (EVs) in cerebrospinal fluid (CSF) showing promise for the assessment of central nervous system (CNS) disorders without actual tissue biopsy and as a complement to imaging techniques. EVs carry molecular cargo such as proteins, nucleic acids, and lipids that mirror those at the tissue of origin, offering unique opportunities to quantify disease-related changes in biomarkers. Compared with plasma-derived EVs, those from CSF provide more direct insights into the CNS because of direct shedding of brain EVs to CSF and bypass of confounding factors involving entry to systemic circulation. Despite this potential, translation into clinical practice is limited by challenges such as low yields, purity concerns, and lack of standardized isolation protocols. Addressing these difficulties, alongside integrating multiomics approaches, will advance our understanding of EV molecular cargo and their functional roles in CNS diseases. Over time, CSF-derived EVs could become the new driver of precision medicine in neurology, offering biologic insight for both diagnostic and therapeutic applications. This perspective provides a critical evaluation of the current status of EV-based liquid biopsy in CSF and offers recommendations for future research and clinical translation of data from CSF-derived EVs, highlighting their potential to inform physiologically based pharmacokinetic (PBPK) models. This state-of-the-art article evaluates existing evidence and highlights key knowledge gaps.