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"6 markers/5 colors" extended white blood cell differential by flow cytometry.

"6 markers/5 colors" extended white blood cell differential by flow cytometry. Research Abstract Details 

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  • "6 markers/5 colors" extended white blood cell differential by flow cytometry. Abstract Text:

    jean-luc faucherJean-Luc Faucher,charlotte lacronique-gazailleCharlotte Lacronique-Gazaille,elise Elise ,franck trimoreauFranck Trimoreau,magali donnardMagali Donnard,dominique bordessouleDominique Bordessoule,francis lacombeFrancis Lacombe,jean feuillardJean Feuillard,jean-luc faucherJean-Luc Faucher,charlotte lacronique-gazailleCharlotte Lacronique-Gazaille,elise Elise ,franck trimoreauFranck Trimoreau,magali donnardMagali Donnard,dominique bordessouleDominique Bordessoule,francis lacombeFrancis Lacombe,jean feuillardJean Feuillard,

    Electronic white blood cell (WBC) differential by standard cytology (hematology analyzer and visual inspection of blood smears) is limited to five types and identification of abnormal cells is only qualitative, often problematic, poorly reproducible, and labour costing. We present our results on WBC differential by flow cytometry (FCM) with a 6 markers, 5 colors CD36-FITC/CD2-PE+CRTH2-PE/CD19-ECD/CD16-Cy5/CD45-Cy7 combination, on 379 subjects, with detection of 12 different circulating cell types, among them 11 were quantified. Detection of quantitative abnormalities of whole leucocytes, neutrophils, eosinophils, basophils, monocytes, or lymphocytes was comparable by FCM and by standard cytology in terms of sensitivity and specificity. FCM was better than standard cytology in detection and quantification of circulating blast cells or immature granulocytes, with a first lineage orientation in the former case. All cases of lymphocytosis, with lineage assignment, were detected by FCM. FCM identified a group of patients with excess of CD16pos monocytes as those having an inflammatory syndrome. WBC differential by FCM is at least as reliable as by standard cytology. FCM superiority consists in identification and systematic quantification of parameters that cannot be assessed by standard cytology such as lineage orientation of blast cells or lymphocytes, and expression of markers of interest such as CD16 on inflammatory monocytes.

    "6 markers/5 colors" extended white blood cell differential by flow cytometry. Publishing Authors By Initials

    jl faucherJL Faucher,c lacronique-gazailleC Lacronique-Gazaille,e E ,f trimoreauF Trimoreau,m donnardM Donnard,d bordessouleD Bordessoule,f lacombeF Lacombe,j feuillardJ Feuillard,jl faucherJL Faucher,c lacronique-gazailleC Lacronique-Gazaille,e E ,f trimoreauF Trimoreau,m donnardM Donnard,d bordessouleD Bordessoule,f lacombeF Lacombe,j feuillardJ Feuillard,

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    PUBMED ID PMID:

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    "6 markers/5 colors" extended white blood cell differential by flow cytometry. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Cytometry. Part A : the journal of the Internation

    VOLUME: 71

    Page Numbers: 934-44

    Journal Abbreviation: Cytometry A

    ISSN: 1552-4922

    DAY: 24

    MONTH: Nov

    YEAR: 2007

    "6 markers/5 colors" extended white blood cell differential by flow cytometry. Information

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    LANGUAGE: eng

    NlmUniqueID: 101235694

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    Grant and Affiliation Information for "6 markers/5 colors" extended white blood cell differential by flow cytometry.

    AFFILIATION: Laboratoire d'Hématologie, Hôpital Dupuytren, Limoges, France.

    Country: United States

    United States Research PublicationUnited States Research Publication

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    MEDLINETA: Cytometry A

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