骨髓增生异常的免疫表型分析

Marie C. Béné , Jean Feuillard , Bernard Husson , Marc Maynadié , the GEIL
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引用次数: 10

摘要

随着人口的老龄化,骨髓增生异常综合征(MDS)的发病率增加,新的和有希望的治疗方法正在开发。“这些新策略的正确应用依赖于对这些可变和多形性疾病的彻底诊断。细胞学和细胞遗传学被纳入MDS的分层,是两个连续系统的主要分类标准。然而,多参数免疫分型和流式细胞术技术的进展表明,这种方法可能很快成为MDS诊断标准的一部分。本文首先对MDS的特点及其分类的演变进行综述。流式细胞术方法的广泛分析,特别是多参数,然后提出,比较各种策略和他们的输出。目前关于MDS免疫分型的信息表明,白细胞分化抗原表达的几种异常对MDS的诊断和预后非常宝贵。正常骨髓和MDS样本之间更彻底和标准化的比较,包括模式评估,而不是作为子集枚举,应该很快进一步为这些疾病的定义和结果预测提供有效的工具。骨髓增生异常疾病(MDS)的诊断目前依赖于细胞学特征和核型异常。这些方法允许使用当前的分类来区分各种形式的MDS。文献综述表明,在过去的5年中,通过流式细胞术对MDS骨髓进行多参数免疫分型的信息越来越多。这些方法一旦标准化,将为MDS患者的诊断和管理提供额外的有价值的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunophenotyping of Myelodysplasia

As the incidence of myelodysplastic syndromes (MDS) increases with the ageing of the population, new and promising therapeutic approaches are being developed. “Proper application of such new strategies relies on a thorough diagnosis of these variable and pleiomorphic disorders. Cytology and cytogenetics are included in the stratification of MDS, and are the main classification criteria in two successive systems. However, the progress of multiparametric immunophenotyping and flow cytometry techniques suggest that this approach may soon become an inclusive part of the diagnostic criteria of MDS. In this review of the literature, the features of MDS and the evolution of the classification these disorders is first summarized. An extensive analysis of flow cytometry approaches, especially multiparametric, is then presented, comparing the various strategies and their output.

Current information regarding immunophenotyping of MDS indicates that several anomalies in the expression of leukocyte differentiation antigens are invaluable for their diagnosis and prognosis. A more thorough and standardized comparison between normal bone marrow and MDS samples, including pattern evaluation rather than as subset enumeration, should soon further provide an efficient tool for the definition and outcome prediction of these diseases. The diagnosis of myelodysplastic disorders (MDS) currently relies on cytological features and karyotypic anomalies. These methods allow using current classifications to discriminate between the various forms of MDS. A review of the literature demonstrates that the past 5 years have seen increasing information regarding multiparametric immunophenotyping of MDS bone marrow by flow cytometry. These approaches, once standardized, should provide an additional valuable tool for the diagnosis and management of MDS patients.

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