Storb R, Prentice R L, Thomas E D
N Engl J Med. 1977 Jan 13;296(2):61-6. doi: 10.1056/NEJM197701132960201.
Seventy-three consecutive patients with severe aplastic anemia were treated by marrow grafts from normal, HLA-identical siblings, and 68 lived long enough to demonstrate engraftment. In 21 patients the garft was rejected, and 19 of these patients died. This analysis, using a binary logistic regression model, was aimed at identifying factors that predicted marrow-graft rejection. Of the 24 factors entered into the analysis, only two strongly correlated with graft rejection: a positive relative response index in mixed leukocyte culture indicating sensitization of patient against donor (P less than 0.01); and a low number of marrow cells ( less than 3 X 10(8) cells per kilogram) used for transplantation (P less than 0.01). These findings suggest that more powerful immunosuppressive conditioning regimens should be used in patients who are sensitized, and that the greatest possible amount of donor marrow, perhaps supplemented by stem cells derived from the peripheral blood, should be obtained.
73例连续性严重再生障碍性贫血患者接受了来自 HLA 相同的正常同胞的骨髓移植,其中68例存活时间足够长以证明植入成功。21例患者发生移植排斥,其中19例死亡。本分析采用二元逻辑回归模型,旨在确定预测骨髓移植排斥的因素。纳入分析的24个因素中,只有两个与移植排斥密切相关:混合淋巴细胞培养中相对反应指数为阳性,表明患者对供体敏感(P<0.01);以及用于移植的骨髓细胞数量少(每千克少于3×10⁸个细胞)(P<0.01)。这些发现表明,对于已致敏的患者应采用更强有力的免疫抑制预处理方案,并且应获取尽可能多的供体骨髓,或许可补充外周血来源的干细胞。