Millar B C, Millar J L, Shepherd V, Blackwell P, Porter H, Cunningham D, Judson I, Treleaven J, Powles R L, Catovsky D
Section of Academic Haematology, McElwain Laboratories, Institute of Cancer Research, Sutton, Surrey, UK.
Bone Marrow Transplant. 1998 Sep;22(5):469-75. doi: 10.1038/sj.bmt.1701368.
The study was designed to determine whether the number of CD34+/CD33- cells given at autologous peripheral blood stem cell (PBSC) rescue after intensive therapy for cancer was a better predictor of platelet engraftment than the total number of CD34+ cells infused. Comparison between the total number of CD34+ cells/kg infused with the number of CD34+/CD33- cells/kg infused showed that, generally, 2 x 10(6) total CD34+ cells contained 1.38 x 10(6) CD34+/CD33- cells. There was poor correlation between the number of CD34+/CD33- and CD34+/CD33+ cells in the graft (r = 0.332). Engraftment times for platelets and neutrophils were evaluated in 68 patients. There was no significant difference between the times for platelets to reach >25 x 10(9)/l or neutrophils to reach >0.5 x 10(9)/l among patients who received > or <2 x 10(6) total CD34+ cells or > or <1.38 x 10(6) CD34+/CD33- cells although the latter was consistently the better predictor. Platelet recovery to >50 x 10(9)/l and >100 x 10(9)/l was delayed significantly in patients who received <1.38 x 10(6) CD34+/CD33-/kg infused (P < 0.02 and P < 0.05, respectively). The number of CD34+/CD33- cells/kg infused was a stronger predictor of platelet recovery than the total number of CD34+ cells infused (P < 0.05 for platelets >50 or >100 x 10(9)/l). Although platelet recovery was delayed significantly in patients who had <4 x 10(4) granulocyte-macrophage colony-forming units (CFU-GM)/kg infused, the time delay between receipt of PBSCs and availability of the colony counts limits the use of this assay to patients who do not require stem cells to be given immediately. Our data suggest that the number of CD34+/CD33- cells given at PBSC rescue provide information about the quality of the graft necessary for long-term platelet engraftment. However, since the percentage of CD34+/CD33- cells shows considerable inter-patient variation, measurement of this cell population may be important in patients who experience poor stem cell mobilization or when a target dose of 2 x 10(6) total CD34+ cells/kg is not achieved.
本研究旨在确定在癌症强化治疗后的自体外周血干细胞(PBSC)救援中,给予的CD34+/CD33-细胞数量是否比输注的CD34+细胞总数更能预测血小板植入情况。比较每千克输注的CD34+细胞总数与每千克输注的CD34+/CD33-细胞数量发现,一般来说,2×10⁶个总CD34+细胞中含有1.38×10⁶个CD34+/CD33-细胞。移植物中CD34+/CD33-细胞与CD34+/CD33+细胞数量之间的相关性较差(r = 0.332)。对68例患者的血小板和中性粒细胞植入时间进行了评估。在接受>或<2×10⁶个总CD34+细胞或>或<1.38×10⁶个CD34+/CD33-细胞的患者中,血小板达到>25×10⁹/L或中性粒细胞达到>0.5×10⁹/L的时间没有显著差异,尽管后者一直是更好的预测指标。接受<1.38×10⁶个CD34+/CD33-/kg输注的患者,血小板恢复到>50×10⁹/L和>100×10⁹/L明显延迟(分别为P < 0.02和P < 0.05)。每千克输注的CD34+/CD33-细胞数量比输注的CD34+细胞总数更能有力地预测血小板恢复情况(对于血小板>50或>100×10⁹/L,P < 0.05)。尽管接受<4×10⁴个粒细胞-巨噬细胞集落形成单位(CFU-GM)/kg输注的患者血小板恢复明显延迟,但从接受PBSC到获得集落计数之间的时间延迟限制了该检测方法在不需要立即给予干细胞的患者中的应用。我们的数据表明,PBSC救援时给予的CD34+/CD33-细胞数量提供了关于长期血小板植入所需移植物质量的信息。然而,由于CD34+/CD33-细胞的百分比在患者之间存在相当大的差异,对于干细胞动员不佳的患者或未达到每千克2×10⁶个总CD34+细胞目标剂量的患者,测量这一细胞群体可能很重要。