Controlling laboratory variables to improve precision and accuracy of CD4+ T-cell enumeration across flow cytometry methods

dc.contributor.authorMandy, Wilja Mirembe
dc.date.accessioned2010-04-13T13:07:46Z
dc.date.available2010-04-13T13:07:46Z
dc.date.issued2010-04-13T13:07:46Z
dc.descriptionMSc (Med), Molecular Medicine and Haematology, Faculty of Health Sciences, University of the Witwatersrand, 2009en_US
dc.description.abstractThis study assessed the effect that certain logistical and methodological factors in the laboratory could have on influencing precision and accuracy of enumeration of CD4+ cells. The efficacy of a new blood stabiliser to extend the window of CD4 testing, was also evaluated. CD4+ counts were derived using the 2-colour Pan-leucogating, 4-colour TetraONE and MultiTEST/TruCount protocols on the EPICS-XL, FC-500 or FACSCalibur flow cytometers. Statistical analyses included the paired-t-test, Spearman’s correlation and Bland Altman comparisons. The results showed that the reliability of CD4+ count results was heavily dependent on how blood samples were handled prior to and after receipt into the laboratory and on how samples were processed and analysed. The factors, motion, operator pipetting and analysis skills, storage temperature, use of different protocols, different gating strategies and the use of different flow cytometers, were found to influence accurate and precise enumeration of CD4+ counts.en_US
dc.identifier.urihttp://hdl.handle.net/10539/7975
dc.language.isoenen_US
dc.subjectCD4 testingen_US
dc.subjectblood stabiliseren_US
dc.subjecthandling of blood samplesen_US
dc.titleControlling laboratory variables to improve precision and accuracy of CD4+ T-cell enumeration across flow cytometry methodsen_US
dc.typeThesisen_US
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