Extracellular vesicles: pathogenetic, diagnostic and therapeutic value in traumatic brain injury

dc.contributor.authorMondello, Stefania
dc.contributor.authorThelin, Eric Peter
dc.contributor.authorShaw, Gerry P.J.
dc.contributor.authorSALZET, Michel
dc.contributor.authorVisalli, Carmela
dc.contributor.authorČí̌zková, Dáša
dc.contributor.authorKobeissy, Firas H.
dc.contributor.authorBuki, Andras
dc.contributor.departmentBiochemistry and Molecular Genetics
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:37:58Z
dc.date.available2025-01-24T11:37:58Z
dc.date.issued2018
dc.description.abstractIntroduction: Traumatic brain injury (TBI) is a leading cause of death and disability worldwide. Accurate classification according to injury-specific and patient-specific characteristics is critical to help informed clinical decision-making and to the pursuit of precision medicine in TBI. Reliable biomarker signatures for improved TBI diagnostics are required but still an unmet need. Areas covered: Extracellular vesicles (EVs) represent a new class of biomarker candidates in TBI. These nano-sized vesicles have key roles in cell signaling profoundly impacting pathogenic pathways, progression and long-term sequelae of TBI. As such EVs might provide novel neurobiological insights, enhance our understanding of the molecular mechanisms underlying TBI pathophysiology and recovery, and serve as biomarker signatures and therapeutic targets and delivery systems. Expert commentary: EVs are fast gaining momentum in TBI research, paving the way for new transformative diagnostic and treatment approaches. Their potential to sort out TBI variability and active involvement in the mechanisms underpinning different clinical phenotypes point out unique opportunities for improved classification, risk-stratification ad intervention, harboring promise of predictive, personalized, and even preemptive therapeutic strategies. Although a great deal of progress has been made, substantial efforts are still required to ensure the needed rigorous validation and reproducibility for clinical implementation of EVs. © 2018 Informa UK Limited, trading as Taylor & Francis Group.
dc.identifier.doihttps://doi.org/10.1080/14789450.2018.1464914
dc.identifier.eid2-s2.0-85047508169
dc.identifier.pmid29671356
dc.identifier.urihttp://hdl.handle.net/10938/28942
dc.language.isoen
dc.publisherTaylor and Francis Ltd
dc.relation.ispartofExpert Review of Proteomics
dc.sourceScopus
dc.subjectBiomarker
dc.subjectExosomes
dc.subjectExtracellular vesicles
dc.subjectMicrovesicles
dc.subjectTbi
dc.subjectTraumatic brain injury
dc.subjectAnimals
dc.subjectBiomarkers
dc.subjectBody fluids
dc.subjectBrain injuries, traumatic
dc.subjectHumans
dc.subjectInflammation
dc.subjectBiological marker
dc.subjectBlood clotting
dc.subjectDiagnostic value
dc.subjectDisease exacerbation
dc.subjectExosome
dc.subjectHuman
dc.subjectMembrane microparticle
dc.subjectMesenchymal stem cell transplantation
dc.subjectNeuroprotection
dc.subjectNonhuman
dc.subjectPathogenesis
dc.subjectPhenotype
dc.subjectReview
dc.subjectSignal transduction
dc.subjectAnimal
dc.subjectBody fluid
dc.subjectMetabolism
dc.subjectPathology
dc.titleExtracellular vesicles: pathogenetic, diagnostic and therapeutic value in traumatic brain injury
dc.typeReview

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