Evidence map›Paper›PMID 42681678›Full record

ReviewTranslational neurodegeneration2026

Central nervous system lymphatic network: from the maintenance of brain homeostasis to emerging therapeutic perspectives in neurodegenerative diseases.

Shixin Ding, Jiguang Yang, Ze Wang, Ruiliang Bai, Kuiying Yin, Lei Jin, Maximilian Kueckelhaus, Sven G Meuth, Ming Xiao, Gang Hu

Abstract readReview
In one paragraph

Review in Translational neurodegeneration, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Shixin DingJiangsu Key Laboratory of Neurodegeneration, Nanjing Medical University, Nanjing, 211166, China.
Jiguang YangJiangsu Key Laboratory of Neurodegeneration, Nanjing Medical University, Nanjing, 211166, China.
Ze WangJiangsu Key Laboratory of Neurodegeneration, Nanjing Medical University, Nanjing, 211166, China.
Ruiliang BaiSchool of Brain Science and Brain Medicine & Liangzhu Laboratory, Zhejiang University School of Medicine, Hangzhou, 311121, China.
Kuiying YinLink Sense Laboratory, Nanjing Research Institute of Electronic Technology, Nanjing, 210039, China.
Lei JinDepartment of Plastic and Reconstructive Surgery, Institute of Musculoskeletal Medicine, University Hospital Muenster, 48157, Muenster, Germany.
Maximilian KueckelhausDepartment of Plastic and Reconstructive Surgery, Institute of Musculoskeletal Medicine, University Hospital Muenster, 48157, Muenster, Germany.
Sven G MeuthDepartment of Neurology, University Hospital Muenster, 48157, Muenster, Germany.
Ming XiaoJiangsu Key Laboratory of Neurodegeneration, Nanjing Medical University, Nanjing, 211166, China. mingx@njmu.edu.cn.
Gang HuJiangsu Key Laboratory of Neurodegeneration, Nanjing Medical University, Nanjing, 211166, China. ghu@njmu.edu.cn.

Funding

the China Postdoctoral Science Foundation 2026M792288the National Natural Science Foundation of China 32541014the National Natural Science Foundation of China 82504762the National Natural Science Foundation of China 82574386
6 · The paper itself

Abstract

The brain was long been regarded as an immune-privileged organ with a lack of lymphatic drainage, partly because of the absence of parenchymal lymphatic vessels. This long-held doctrine has been challenged by recent advancements in central lymphatic vascular biology. The central drainage network, which consists of the glymphatic system, meningeal lymphatic vessels, and cranial perineural drainage pathways, plays a crucial role in the clearance of metabolic brain waste and the maintenance of brain homeostasis. Furthermore, the meninges and brain perivascular spaces are rich in immune cells that regulate neuronal activities and diverse behaviors through secretion of cytokines. Dysfunction of the central lymphatic network is widely observed in natural aging and neurodegenerative disorders, which is characterized by mislocalization of aquaporin-4 on astrocytic endfeet, impairment of lymphatic valvular integrity, and alterations in the proportion and phenotype of meningeal immune cells. In this review, we provide a comprehensive overview of the anatomical foundations, molecular regulatory mechanisms, and physiological functions of this system. We summarize the pathological roles of the central lymphatic network across neurodegenerative conditions and discuss emerging clinical assessment frameworks based on multimodal imaging and liquid biomarkers. We also highlight promising therapeutic strategies, such as restoring meningeal lymphatic function, targeting glymphatic drainage, and modulating the meningeal immune microenvironment. Elucidating the dynamics of the central lymphatic network will reshape our understanding of brain homeostasis, paving the way for novel diagnostic and therapeutic strategies for neurodegenerative diseases. Future research should focus on translating fundamental findings into clinical applications, thereby accelerating the transition from basic research to clinical practice.

Indexed as

BrainCentral Nervous SystemGlymphatic SystemHomeostasisLymphatic SystemLymphatic VesselsNeurodegenerative DiseasesAnimalsHumansBrain homeostasisCentral lymphatic networkImmunosurveillanceNeurodegenerative diseasesTherapeutic targets

Identifiers

PMID42681678
PMCPMC13536567

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.