Banno S, Nitta M, Noda T, Komatsu H, Iida S, Takada K, Yamamoto M, Mitomo Y
Department of Hematology, Shizuoka Saiseikai General Hospital.
Rinsho Ketsueki. 1991 Nov;32(11):1469-74.
We report a case involving mixed hematopoietic chimerism after an allogeneic bone marrow transplantation (BMT) from a sex mismatched donor. A 31 year-old-man who was diagnosed as having chronic myelogenous leukemia in the accelerated phase received an allogenic BMT from his HLA-identical sister in March, 1989. To determine the mixed chimerism we used the Y-chromosome specific repeated sequence of DNA using a specific probe (PHY 10). The donor's DNA 3.5 kb band appeared in 1-10% of male DNA by Southern blot hybridization in the peripheral blood 21 days after BMT. The Y-chromosome DNA band decreased day by day, and disappeared 110 days after BMT. The Y-chromosome DNA band could be detected, even though few metaphases were obtained immediately after BMT. Thus this method is very sensitive for determining which cells contain the Y-chromosome, and is therefore useful for detecting mixed chimerism after sex-mismatched BMT. Using this method the clinical significance of mixed chimerism can be assessed.
我们报告了一例在接受来自性别不匹配供体的异基因骨髓移植(BMT)后出现混合造血嵌合体的病例。一名31岁男性,被诊断为处于加速期的慢性粒细胞白血病,于1989年3月接受了来自其 HLA 相同妹妹的异基因BMT。为了确定混合嵌合体,我们使用特异性探针(PHY 10)检测Y染色体特异性DNA重复序列。BMT后21天,通过Southern印迹杂交在外周血中,供体的DNA 3.5 kb条带出现在1 - 10%的男性DNA中。Y染色体DNA条带逐日减少,并在BMT后110天消失。即使在BMT后立即获得的中期细胞很少,Y染色体DNA条带仍可被检测到。因此,该方法对于确定哪些细胞含有Y染色体非常敏感,因此对于检测性别不匹配BMT后的混合嵌合体很有用。使用该方法可以评估混合嵌合体的临床意义。