Tseng Li-Hui, Tang Jih-Luh, Haley Lisa, Beierl Katie, Gocke Christopher D, Eshleman James R, Lin Ming-Tseh
Departments of *Pathology ‡Oncology, Johns Hopkins University School of Medicine, Johns Hopkins Hospital, Baltimore, MD †Department of Medical Genetics and Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Appl Immunohistochem Mol Morphol. 2014 Jul;22(6):416-20. doi: 10.1097/PDM.0000000000000029.
Polymorphic short tandem-repeat, or microsatellite, loci have been widely used to analyze chimerism status after allogeneic hematopoietic stem-cell transplantation. In molecular diagnostic laboratories, it is recommended to calculate mixed chimerism for at least 2 informative loci and to avoid microsatellite loci on chromosomes with copy number changes. In this report, we show that microsatellite instability observed in 2 patients with acute leukemia may confound chimerism analysis. Interpretation errors may occur even if 2 to 3 loci are analyzed because of length variation in multiple microsatellite loci. Although microsatellite loci with length variation should not be selected for chimerism analysis, the presence of microsatellite instability, like copy number alteration because of aberrant chromosomes, provides evidence of recurrent or residual cancer cells after hematopoietic stem-cell transplantation.
多态性短串联重复序列,即微卫星位点,已被广泛用于分析异基因造血干细胞移植后的嵌合状态。在分子诊断实验室中,建议至少计算2个信息位点的混合嵌合率,并避免使用存在拷贝数变化的染色体上的微卫星位点。在本报告中,我们表明在2例急性白血病患者中观察到的微卫星不稳定性可能会混淆嵌合分析。即使分析2至3个位点,由于多个微卫星位点的长度变化,也可能发生解释错误。虽然不应选择具有长度变化的微卫星位点进行嵌合分析,但微卫星不稳定性的存在,就像异常染色体导致的拷贝数改变一样,为造血干细胞移植后复发或残留癌细胞提供了证据。