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出 处:《临床检验杂志》2005年第2期95-97,共3页Chinese Journal of Clinical Laboratory Science
摘 要:目的 探讨荧光标记引物复合扩增短串联重复序列技术(fm PCR -STR)在分析异基因造血干细胞移植(allo- SCT)后植活状态中的作用。方法 用fm -PCR- STR技术对 15例allo SCT患者的 15个STR位点和 1个性别位点 (牙釉蛋白基因 )进行分析。结果 12例(5例接受HLA全相合allo- SCT和 7例接受HLA半相合allo SCT)的受者移植后均持续表达完全供者型。1例HLA全相合allo -SCT和 1例HLA半相合allo -SCT在fm PCR -STR动态观察中早期均表现为完全供者型,分别于+82d和 +381d转为嵌合型。1例HLA半相合首次移植+31d表达完全受者型(反映移植失败),再次移植+29d表达完全供者型。结论 fm -PCR- STR可敏感且精确地分析allo SCT后移植物植活状态,亦可作为白血病复发的监控手段。Objective To evaluate the application of multiplex polymerase chain reaction technique with fluorescence labeling primers for short tandem repeats(fm-PCR-STR) in the detection of engraftment following allogeneic stem cell transplantation (allo-SCT).Methods Fifteen STR loci and a sex-linked loci (amelogenin) were analyzed by fm-PCR-STR in 15 patients with allo-SCT.Results STR of 12 recipients after allo-SCT continuously presented full donor chimeras,among them 5 patients received grafts from HLA identical sibling donor while 7 received from HLA haplotype-mismatched grafts.During the dynamic observation after transplantation a recipient with HLA identical allo-SCT and a HLA haplotype-mismatched allo-SCT got the evidences of survival of engraftment and presented full donor type,but transformed to mixed chimeras later at +82d and +381d respectively.In another case with HLA haplotype-mismatched graft,STR showed full recipient chimeras at +31d after the first allo-SCT,indicating engraftment failure,but showed full donor chimeras at +29d after the second allo-SCT.Conclutions Analysis of fm-PCR-STR following allo-SCT provided a sensitive and accurate indication on engraftment and monitoring the recrudesce of leukaemia.
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