Clinical requirements for extracellular vesicle assays

The scientific and clinical interest in extracellular vesicles (EV) has grown exponentially during the past 15 years. As most research indicates that EVs can be utilised in diagnostics, prognostics and therapeutics, we may be on the brink of establishing the clinical utility of EV measurement, but h...

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Main Authors: Lisa Ayers, Ryan Pink, David Raul Francisco Carter, Rienk Nieuwland
Format: Article
Language:English
Published: Wiley 2019-12-01
Series:Journal of Extracellular Vesicles
Subjects:
Online Access:http://dx.doi.org/10.1080/20013078.2019.1593755
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author Lisa Ayers
Ryan Pink
David Raul Francisco Carter
Rienk Nieuwland
author_facet Lisa Ayers
Ryan Pink
David Raul Francisco Carter
Rienk Nieuwland
author_sort Lisa Ayers
collection DOAJ
description The scientific and clinical interest in extracellular vesicles (EV) has grown exponentially during the past 15 years. As most research indicates that EVs can be utilised in diagnostics, prognostics and therapeutics, we may be on the brink of establishing the clinical utility of EV measurement, but how can we make this a reality? If we are to introduce EVs as biomarkers into clinical laboratories, it will be necessary to offer fully validated, International Organization for Standardization (ISO) standard 15189 assays. ISO 15189 defines the quality management system requirements particular to medical laboratories and is used internationally to determine accreditation. In order for a clinical laboratory to offer an accredited test for EVs, this assay must have been subjected to a thorough assay validation process. This process requires the generation of data related to defined performance characteristics, to ensure that an assay is performing in accordance with the needs of its clinical users. Each of the defined performance characteristics will be discussed in this review, along with the issues that specifically affect EV analysis. Accreditation is increasingly important for all clinical laboratories and the standards required to achieve this are becoming more and more stringent. Therefore, as companies seek to develop the best assays to detect EVs and their molecular contents for clinical utility, and as we move rapidly towards our goal of offering EV analysis in the diagnosis and monitoring of disease, it is timely to highlight the requirements for the clinical accreditation of such assays. It is essential to consider these parameters to ensure that we develop the highest quality assays possible and ultimately the best outcomes for patients.
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spelling doaj.art-4faac9c8c31d48ab892e7d2a015e92d02022-12-22T01:39:53ZengWileyJournal of Extracellular Vesicles2001-30782019-12-018110.1080/20013078.2019.15937551593755Clinical requirements for extracellular vesicle assaysLisa Ayers0Ryan Pink1David Raul Francisco Carter2Rienk Nieuwland3Oxford University Hospitals NHS Foundation TrustOxford Brookes UniversityOxford Brookes UniversityAmsterdam UMC, University of AmsterdamThe scientific and clinical interest in extracellular vesicles (EV) has grown exponentially during the past 15 years. As most research indicates that EVs can be utilised in diagnostics, prognostics and therapeutics, we may be on the brink of establishing the clinical utility of EV measurement, but how can we make this a reality? If we are to introduce EVs as biomarkers into clinical laboratories, it will be necessary to offer fully validated, International Organization for Standardization (ISO) standard 15189 assays. ISO 15189 defines the quality management system requirements particular to medical laboratories and is used internationally to determine accreditation. In order for a clinical laboratory to offer an accredited test for EVs, this assay must have been subjected to a thorough assay validation process. This process requires the generation of data related to defined performance characteristics, to ensure that an assay is performing in accordance with the needs of its clinical users. Each of the defined performance characteristics will be discussed in this review, along with the issues that specifically affect EV analysis. Accreditation is increasingly important for all clinical laboratories and the standards required to achieve this are becoming more and more stringent. Therefore, as companies seek to develop the best assays to detect EVs and their molecular contents for clinical utility, and as we move rapidly towards our goal of offering EV analysis in the diagnosis and monitoring of disease, it is timely to highlight the requirements for the clinical accreditation of such assays. It is essential to consider these parameters to ensure that we develop the highest quality assays possible and ultimately the best outcomes for patients.http://dx.doi.org/10.1080/20013078.2019.1593755extracellular vesiclesclinical assaysaccreditationiso 15189standardisationvalidationverification
spellingShingle Lisa Ayers
Ryan Pink
David Raul Francisco Carter
Rienk Nieuwland
Clinical requirements for extracellular vesicle assays
Journal of Extracellular Vesicles
extracellular vesicles
clinical assays
accreditation
iso 15189
standardisation
validation
verification
title Clinical requirements for extracellular vesicle assays
title_full Clinical requirements for extracellular vesicle assays
title_fullStr Clinical requirements for extracellular vesicle assays
title_full_unstemmed Clinical requirements for extracellular vesicle assays
title_short Clinical requirements for extracellular vesicle assays
title_sort clinical requirements for extracellular vesicle assays
topic extracellular vesicles
clinical assays
accreditation
iso 15189
standardisation
validation
verification
url http://dx.doi.org/10.1080/20013078.2019.1593755
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