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Establishment of the first World Health Organization International Genetic Reference Panel for quantitation of BCR-ABL mRNA

机译:成立首个世界卫生组织国际遗传参考委员会,对BCR-ABL mRNA进行定量

摘要

Serial quantitation of BCR-ABL mRNA levels is an important indicator of therapeutic response for patients with chronic myelogenous leukemia and Philadelphia chromosome-positive acute lymphoblastic leukemia, but there is substantial variation in the real-time quantitative polymerase chain reaction methodologies used by different testing laboratories. To help improve the comparability of results between centers we sought to develop accredited reference reagents that are directly linked to the BCR-ABL international scale. After assessment of candidate cell lines, a reference material panel comprising 4 different dilution levels of freezedried preparations of K562 cells diluted in HL60 cells was prepared. After performance evaluation, the materials were assigned fixed percent BCR-ABL/control gene values according to the International Scale. A recommendation that the 4 materials be established as the first World Health Organization International Genetic Reference Panel for quantitation of BCR-ABL translocation by real-time quantitative polymerase chain reaction was approved by the Expert Committee on Biological Standardization of the World Health Organization in November 2009. We consider that the development of these reagents is a significant milestone in the standardization of this clinically important test, but because they are a limited resource we suggest that their availability is restricted to manufacturers of secondary reference materials. © 2010 by The American Society of Hematology.
机译:BCR-ABL mRNA水平的连续定量是慢性粒细胞性白血病和费城染色体阳性急性淋巴细胞白血病患者治疗反应的重要指标,但不同测试实验室使用的实时定量聚合酶链反应方法存在很大差异。为了帮助提高各研究中心之间结果的可比性,我们寻求开发与BCR-ABL国际标准直接相关的认可参考试剂。在评估候选细胞系之后,制备了包含4种不同稀释水平的在HL60细胞中稀释的K562细胞冻干制剂的参考材料组。在性能评估后,根据国际标准为材料分配了固定百分比的BCR-ABL /对照基因值。 2009年11月,世界卫生组织生物标准化专家委员会批准了一项建议,即建立这4种材料作为世界卫生组织首个通过实时定量聚合酶链反应定量BCR-ABL易位的国际遗传参考小组。我们认为这些试剂的开发是该临床重要测试标准化的一个重要里程碑,但是由于它们的资源有限,因此我们建议将其可用性限于二级参考材料的制造商。 ©2010,美国血液学会。

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