Publication:
High-Sensitivity Flow Cytometry for the Reliable Detection of Measurable Residual Disease in Hematological Malignancies in Clinical Laboratories.

dc.contributor.authorÁlvarez Flores, María Beatriz
dc.contributor.authorSopeña Corvinos, María
dc.contributor.authorGuillén Santos, Raquel
dc.contributor.authorCava Valenciano, Fernando
dc.contributor.funderCentro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC) (España)
dc.contributor.funderMinisterio de Ciencia e Innovación (España)
dc.contributor.funderMinisterio de Ciencia e Innovación. Centro de Excelencia Severo Ochoa (España)
dc.date.accessioned2025-01-23T16:02:15Z
dc.date.available2025-01-23T16:02:15Z
dc.date.issued2024-12-22
dc.descriptionThis publication was funded by the Centro Nacional de Investigaciones Cardiovasculares (CNIC). The CNIC is supported by the Instituto de Salud Carlos III (ISCIII), the Ministerio de Ciencia e Innovación (MCIN), and the Pro CNIC Foundation and is a Severo Ochoa Center of Excellence (grant CEX2020-001041-S funded by MICIN/AEI/10.13039/501100011033).
dc.description.abstractMonitoring of measurable residual disease (MRD) requires highly sensitive flow cytometry protocols to provide an accurate prediction of shorter progression-free survival. High assay sensitivity generally requires rapid processing to avoid cell loss from small bone marrow sample volumes, but this requirement conflicts with the need in most clinical cytometry laboratories for long processing and acquisition times, especially when multiple MRD studies coincide on the same day. The proposed protocol was applied to 226 human bone marrow and 45 peripheral blood samples submitted for the study of MRD or the detection of rare cells. Samples were processed within 24 h of extraction and acquired with an eight-color flow cytometer. The FACSLyse-Bulk protocol allows for the labelling of millions of cells in under 90 min in small sample volumes without affecting the FSC/SSC pattern or antigen expression, and it also allows antigens to be fixed to the membrane, thus avoiding the capping phenomenon. The proposed protocol would allow clinical flow cytometry laboratories to perform MRD studies in house and easily achieve a limit of detection and limit of quantification <0.001%, thus avoiding the need to outsource analysis to specialized cytometry laboratories.
dc.description.peerreviewed
dc.format.number(12)
dc.format.page338
dc.format.volume12
dc.identifier.citationDiseases. 2024 Dec 22;12(12):338.
dc.identifier.journalDiseases
dc.identifier.pubmedID39727668
dc.identifier.urihttps://hdl.handle.net/20.500.12105/26118
dc.language.isoeng
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI)
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/MICIN/AEI/10.13039/501100011033
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/CEX2020-001041-S
dc.relation.publisherversionhttps://10.3390/diseases12120338
dc.repisalud.institucionCNIC
dc.repisalud.orgCNICCitometría de Flujo
dc.rights.accessRightsopen access
dc.rights.licenseAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectbone marrow
dc.subjectflow cytometry
dc.subjecthematology
dc.subjecthigh-sensitivity flow cytometry
dc.subjectleukemia
dc.subjectlimit of detection
dc.subjectlymphoma
dc.subjectmastocytosis
dc.subjectmeasurable residual disease
dc.subjectmultiple myeloma
dc.subjectstaining and labeling
dc.titleHigh-Sensitivity Flow Cytometry for the Reliable Detection of Measurable Residual Disease in Hematological Malignancies in Clinical Laboratories.
dc.typeresearch article
dc.type.hasVersionVoR
dspace.entity.typePublication

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