Evidence map›Paper›PMID 34445717›Full record

ReviewInternational journal of molecular sciences2021

Potential Roles of Extracellular Vesicles as Biomarkers and a Novel Treatment Approach in Multiple Sclerosis.

María Gutiérrez-Fernández, Fernando de la Cuesta, Antonio Tallón, Inmaculada Cuesta, Mireya Fernández-Fournier, Fernando Laso-García, Mari Carmen Gómez-de Frutos, Exuperio Díez-Tejedor, Laura Otero-Ortega

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  3. In-Depth Characterization of L1CAMInternational journal of molecular sciences · 2025
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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

9 authors at 1 institution in 1 country.

María Gutiérrez-FernándezNeurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neuroscience Area of IdiPAZ Health Research Institute, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.
Fernando de la CuestaDepartment of Pharmacology and Therapeutics, School of Medicine, Universidad Autónoma de Madrid, 28046 Madrid, Spain.ORCID 0000-0001-8761-7713
Antonio TallónNeurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neuroscience Area of IdiPAZ Health Research Institute, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.
Inmaculada CuestaNeurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neuroscience Area of IdiPAZ Health Research Institute, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.
Mireya Fernández-FournierNeurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neuroscience Area of IdiPAZ Health Research Institute, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.
Fernando Laso-GarcíaNeurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neuroscience Area of IdiPAZ Health Research Institute, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.ORCID 0000-0002-5481-0514
Mari Carmen Gómez-de FrutosNeurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neuroscience Area of IdiPAZ Health Research Institute, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.
Exuperio Díez-TejedorNeurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neuroscience Area of IdiPAZ Health Research Institute, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.
Laura Otero-OrtegaNeurological Sciences and Cerebrovascular Research Laboratory, Department of Neurology, Neuroscience Area of IdiPAZ Health Research Institute, La Paz University Hospital, Universidad Autónoma de Madrid, 28046 Madrid, Spain.ORCID 0000-0001-8765-6341
Universidad Autónoma de Madrid · ES

Funding

ERDF CP15/00069; CPII20/00002 ,CP20/00024, FI17/00188 , FI18/00026Instituto de salud carlos III FI18/00026Instituto de Salud Carlos III CP15/00069Instituto de Salud Carlos III CP20/00024Instituto de Salud Carlos III CPII20/00002Instituto de Salud Carlos III FI17/00188Talent Advanced Researchers' Grant 2019-T1/IND-13794
6 · The paper itself

Abstract

Extracellular vesicles (EVs) are a heterogeneous group of bilayer membrane-wrapped molecules that play an important role in cell-to-cell communication, participating in many physiological processes and in the pathogenesis of several diseases, including multiple sclerosis (MS). In recent years, many studies have focused on EVs, with promising results indicating their potential role as biomarkers in MS and helping us better understand the pathogenesis of the disease. Recent evidence suggests that there are novel subpopulations of EVs according to cell origin, with those derived from cells belonging to the nervous and immune systems providing information regarding inflammation, demyelination, axonal damage, astrocyte and microglia reaction, blood-brain barrier permeability, leukocyte transendothelial migration, and ultimately synaptic loss and neuronal death in MS. These biomarkers can also provide insight into disease activity and progression and can differentiate patients' disease phenotype. This information can enable new pathways for therapeutic target discovery, and consequently the development of novel treatments. Recent evidence also suggests that current disease modifying treatments (DMTs) for MS modify the levels and content of circulating EVs. EVs might also serve as biomarkers to help monitor the response to DMTs, which could improve medical decisions concerning DMT initiation, choice, escalation, and withdrawal. Furthermore, EVs could act not only as biomarkers but also as treatment for brain repair and immunomodulation in MS. EVs are considered excellent delivery vehicles. Studies in progress show that EVs containing myelin antigens could play a pivotal role in inducing antigen-specific tolerance of autoreactive T cells as a novel strategy for the treatment as "EV-based vaccines" for MS. This review explores the breakthrough role of nervous and immune system cell-derived EVs as markers of pathological disease mechanisms and potential biomarkers of treatment response in MS. In addition, this review explores the novel role of EVs as vehicles for antigen delivery as a therapeutic vaccine to restore immune tolerance in MS autoimmunity.

Indexed as

AstrocytesBiomarkers, PharmacologicalBlood-Brain BarrierBrainCell CommunicationExtracellular VesiclesHumansMicrogliaMultiple SclerosisBiomarkers, Pharmacologicalantigen delivery systembiomarkersextracellular vesiclesmultiple sclerosisresponse to treatmentvaccine-like treatment

Identifiers

PMID34445717
PMCPMC8396540
OpenAlexW3196064572

What OpenQuestion holds

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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 OpenQuestion graph.