2021
DOI: 10.3390/mps4020024
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Assessment of Protocol Impact on Subjectivity Uncertainty When Analyzing Peripheral Blood Mononuclear Cell Flow Cytometry Data Files

Abstract: Measured variability of product within Cell and Gene Therapy (CGT) manufacturing arises from numerous sources across pre-analytical to post-analytical phases of testing. Operators are a function of the manufacturing process and are an important source of variability as a result of personal differences impacted by numerous factors. This research uses measurement uncertainty in comparison to Coefficient of Variation to quantify variation of participants when they complete Flow Cytometry data analysis through a 5… Show more

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Cited by 3 publications
(3 citation statements)
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“…However, this approach is flawed without a gold standard or if said standard comes with substantial measurement error. As with all laboratory measures, there may be measurement error in flow cytometry counts [18]. Instead, we assess model performance by quantifying how much of the variance in whole blood DNAm levels is explained by the various cell proportion estimates.…”
Section: Discussionmentioning
confidence: 99%
“…However, this approach is flawed without a gold standard or if said standard comes with substantial measurement error. As with all laboratory measures, there may be measurement error in flow cytometry counts [18]. Instead, we assess model performance by quantifying how much of the variance in whole blood DNAm levels is explained by the various cell proportion estimates.…”
Section: Discussionmentioning
confidence: 99%
“…Isolated lymphocytes (2×10 6 cells/mL; 50 μL) were stained using mouse anti-chicken CD3 + -allophycocyanin (APC), CD4 + -fluorescein isothiocyanate (FITC), and CD8 + -phycoerythrin (PE) fluorescent antibodies. The percentage of CD4 + and CD8 + T lymphocytes in T cells was measured by florescence-activated cell sorting (FACS; BD FACSVerseTM, CA, USA), and the ratio of CD4 + /CD8 + T cells was calculated ( 21 ).…”
Section: Methodsmentioning
confidence: 99%
“…Flow cytometry assays detecting NET components on cells or EVs have also been proposed for the assessment of NET formation in vivo in both animal models and humans [25,36]. However, these methods are hampered by a lack of standardization and operator subjectivity during the data-analysis stage [37]. Enzyme-linked immunosorbent assays (ELISAs), both commercial and in-house, can be used to quantify NET components in blood.…”
Section: Neutrophil Extracellular Traps (Nets)mentioning
confidence: 99%