Goldmann S F
Klin Padiatr. 1981 May;193(3):266-71. doi: 10.1055/s-2008-1034474.
Patient survival after BMT is directly correlated with the HLA-type of the donor. The survival rate after BMT from an HLA-genotypically identical sibling is 56% in acute leukemia, 55% in combined severe immunodeficiency disease (SCID) and 67/83% in severe aplastic anemia patients. The usage of only HLA-D identical related or unrelated donors in SCID revealed a 37% survival, compared to 18% survival in acute leukemia and 11% in severe aplastic anemia using HLA-phenotypical identical or HLA-D identical related donors. BMT from HLA-phenotypical and MLC identical unrelated donors resulted in death of the grafted patients. Non of the patients grafted with HLA-different marrow survived BMT. Survival of BMT patients depended beside the histocompatibility matching on the clinical treatment and the clinical constellation of the patient: The survival rate decreased in aplastic anemia patients due to sensibilisation caused by pre-BMT blood transfusion and was significantly higher in leukemia when BMT was performed in remission.
骨髓移植(BMT)后患者的生存率与供体的人类白细胞抗原(HLA)类型直接相关。在急性白血病中,来自HLA基因相同的同胞供体进行BMT后的生存率为56%,在联合严重免疫缺陷病(SCID)中为55%,在重型再生障碍性贫血患者中为67/83%。在SCID中仅使用HLA-D相同的相关或无关供体进行BMT的生存率为37%,相比之下,在急性白血病中使用HLA表型相同或HLA-D相同的相关供体进行BMT的生存率为18%,在重型再生障碍性贫血中为11%。来自HLA表型和混合淋巴细胞培养(MLC)相同的无关供体的BMT导致移植患者死亡。接受HLA不同骨髓移植的患者无一在BMT后存活。BMT患者的生存除了取决于组织相容性匹配外,还取决于临床治疗和患者的临床情况:由于BMT前输血引起的致敏,再生障碍性贫血患者的生存率下降,而在缓解期进行BMT时,白血病患者的生存率显著更高。