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首页> 外文期刊>Bone marrow transplantation >Platelet chimerism by polymerase chain reaction (PCR) utilizing variable number of tandem repeats (VNTR) in allogeneic stem cell transplant in children: a new novel approach to full chimerism analysis.
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Platelet chimerism by polymerase chain reaction (PCR) utilizing variable number of tandem repeats (VNTR) in allogeneic stem cell transplant in children: a new novel approach to full chimerism analysis.

机译:在儿童同种异体干细胞移植中利用可变数目的串联重复序列(VNTR)的聚合酶链反应(PCR)进行血小板嵌合:完全嵌合分析的新方法。

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摘要

Summary:Evaluation of chimerism following allogeneic transplantation has been performed traditionally focusing on two cellular compartments, namely lymphoid and myeloid. However, none has been described so far to evaluate platelet chimerism. In order to achieve full chimerism in all three cellular compartments, we prospectively obtained 138 samples of peripheral blood in 55 patients at different post transplant periods following allogeneic hematopoietic transplantation. Evaluation of chimerism was performed utilizing tests of variable number of tandem repeat (VNTR) and sex determination by quantitative polymerase chain reaction (PCR). Tests for platelet chimerism using platelet-rich plasma were simultaneously analyzed with samples for T-cell lymphoid and myeloid compartments. Complete donor chimerism was noted in 49 of 55 patients (89%), while the remaining six have split chimerism ranging from 34 to 98%. There is significant difference (P=0.0004) between the percentages of donor DNA in all three cellular compartments comparing the means+/-s.e.m. (myeloid 95.60+/-0.9, T-cell lymphocytes 87.6+/-1.9, and the platelets 90.8+/-1.5); however, comparison between the medians is not statistically significant. This study represents an additional step towards achieving full chimerism and the observation may help reduce the number of unnecessary platelet transfusions once chimerism is noted in that cellular compartment.Bone Marrow Transplantation (2003) 32, 825-828. doi:10.1038/sj.bmt.1704236
机译:摘要:同种异体移植后的嵌合状态评估通常集中于两个细胞区室,即淋巴和髓样。但是,到目前为止,还没有任何文献描述过评估血小板嵌合症。为了在所有三个细胞区室中实现完全嵌合,我们预期在异基因造血移植后不同移植后时期的55位患者中获得138个外周血样品。利用可变数目的串联重复序列(VNTR)的测试和通过定量聚合酶链反应(PCR)的性别确定来进行嵌合性的评估。同时使用样本中的T细胞淋巴和髓样区室对使用富含血小板的血浆进行的血小板嵌合测试进行了分析。 55位患者中有49位(89%)发现完全的供体嵌合,而其余6位的分裂嵌合率则在34%至98%之间。比较平均值+/- s.e.m,在所有三个细胞区室中供体DNA的百分比之间存在显着差异(P = 0.0004)。 (骨髓95.60 +/- 0.9,T细胞淋巴细胞87.6 +/- 1.9,血小板90.8 +/- 1.5);但是,中位数之间的比较在统计上并不显着。该研究代表了实现完全嵌合的又一步骤,一旦在该细胞区室中发现嵌合现象,该观察结果可能有助于减少不必要的血小板输注。骨髓移植(2003)32,825-828。 doi:10.1038 / sj.bmt.1704236

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