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巴西流式细胞术小组-GBCFLUX首次提出了用于急性白血病四色免疫表型分析的流式细胞术检测方案。

First proposed panels on acute leukemia for four-color immunophenotyping by flow cytometry from the Brazilian group of flow cytometry-GBCFLUX.

作者信息

Ikoma Maura R V, Sandes Alex F, Thiago Leandro S, Cavalcanti Júnior Geraldo B, Lorand-Metze Irene G H, Costa Elaine S, Pimenta Glicinia, Santos-Silva Maria C, Bacal Nydia S, Yamamoto Mihoko, Souto Elizabeth X

机构信息

Hospital Amaral Carvalho, Laboratório de Citometria de Fluxo do Hemonúcleo Regional de Jau, São Paulo, Brazil.

出版信息

Cytometry B Clin Cytom. 2015 May-Jun;88(3):194-203. doi: 10.1002/cyto.b.21175. Epub 2014 Apr 19.

Abstract

Multiparameter flow cytometry is a highly sensitive, fast, and specific diagnostic technology with a wide range of applicability in hematology. Although well-established eight-color immunophenotyping panels are already available, most Brazilian clinical laboratories are equipped with four-color flow cytometer facilities. Based on this fact, the Brazilian Group of Flow Cytometry (Grupo Brasileiro de Citometria de Fluxo, GBCFLUX) for standardization of clinical flow cytometry has proposed an antibody panel designed to allow precise diagnosis and characterization of acute leukemia (AL) within resource-restricted areas. Morphological analysis of bone marrow smears, together with the screening panel, is mandatory for the primary identification of AL. The disease-oriented panels proposed here are divided into three levels of recommendations (mandatory, recommendable, and optional) in order to provide an accurate final diagnosis, as well as allow some degree of flexibility based on available local resources and patient-specific needs. The proposed panels will be subsequently validated in an interlaboratory study to evaluate its effectiveness on the diagnosis and classification of AL. (Assoc editor comm. 2).

摘要

多参数流式细胞术是一种高度灵敏、快速且特异的诊断技术,在血液学领域具有广泛的适用性。尽管成熟的八色免疫表型分析试剂盒已经存在,但大多数巴西临床实验室配备的是四色流式细胞仪设备。基于这一事实,巴西流式细胞术标准化组织(巴西流式细胞术小组,GBCFLUX)提出了一组抗体,旨在使资源有限地区能够精确诊断和鉴定急性白血病(AL)。骨髓涂片的形态学分析以及筛查试剂盒对于AL的初步识别是必不可少的。这里提出的针对疾病的试剂盒分为三个推荐级别(强制、推荐和可选),以便提供准确的最终诊断,并根据当地可用资源和患者的特定需求具有一定程度的灵活性。随后,这些提议的试剂盒将在一项实验室间研究中进行验证,以评估其对AL诊断和分类的有效性。(副主编评论2)

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