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基于 SYBR Green 的 qRT-PCR 定量检测 16 个与 post hSCT 嵌合体相关的 SNP 等位基因特异性。

Evaluation of 16 SNPs allele-specific to quantify post hSCT chimerism by SYBR green-based qRT-PCR.

机构信息

Department of Clinical and Experimental Oncology, Universidade Federal de São Paulo (UNIFESP), São Paulo/SP, Brazil.

出版信息

J Clin Pathol. 2013 Mar;66(3):238-42. doi: 10.1136/jclinpath-2012-201224. Epub 2013 Jan 2.

DOI:10.1136/jclinpath-2012-201224
PMID:23288918
Abstract

The importance of monitoring post haematopoietic stem cell transplantation (hSCT) chimerism has been defined in numerous publications. Single-nucleotide polymorphisms (SNPs) are molecular markers that vary significantly among different populations. Allied to a very sensible technique, SNP assays seem to be very sensitive (0.001%) when post hSCT chimerism is measured. However, well known SNP frequencies are limited to certain populations, mainly in countries where there is a high level of diversity in its population, therefore restricting their use worldwide. Amplification by SYBR green based quantitative real time PCR of eight pairs of allele-specific SNPs (MLH-1, PECAM-1, ICAM-1, SUR-1, HA-1, rs715405, rs713503, rs2296600) was conducted in 88 patient/donor pairs, who underwent allogeneic myeloablative or non-myeloablative hSCT. One informative allele was detected in at least 42% (n=37) of the samples; 20% (n=18) had at least two informative alleles; 10% (n=9) had at least three informative alleles; 9% (n=8) had more than three informative alleles and 18% (n=16) showed no informative allele at all. Overall, the frequency of informative alleles for these SNPs in the Brazilian population was very low. Consequently, the amount of information attained reached 9% of those expected, being able to discriminate only eight pairs of donor/recipient samples with more than three informative alleles, making them useless for the quantification of chimerism in our routine.

摘要

监测造血干细胞移植(HSCT)后嵌合体的重要性已在众多出版物中得到定义。单核苷酸多态性(SNP)是在不同人群中差异显著的分子标志物。与非常合理的技术相结合,SNP 检测在测量 HSCT 后嵌合体时似乎非常敏感(0.001%)。然而,众所周知的 SNP 频率仅限于某些人群,主要是在人口多样性水平较高的国家,因此限制了它们在全球范围内的使用。对 88 对患者/供体进行了基于 SYBR 绿色的等位基因特异性 SNP(MLH-1、PECAM-1、ICAM-1、SUR-1、HA-1、rs715405、rs713503、rs2296600)的扩增,这些患者/供体接受了同种异体清髓或非清髓 HSCT。至少在 42%(n=37)的样本中检测到一个信息性等位基因;20%(n=18)至少有两个信息性等位基因;10%(n=9)至少有三个信息性等位基因;9%(n=8)有三个以上的信息性等位基因;18%(n=16)完全没有信息性等位基因。总的来说,这些 SNP 在巴西人群中的信息性等位基因频率非常低。因此,获得的信息量仅为预期的 9%,只能区分出 8 对具有三个以上信息性等位基因的供体/受体样本,使其无法用于我们常规的嵌合体定量。

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