Ojeda-Uribe M, Sovalat H, Bourderont D, Brunot A, Marr A, Lewandowski H, Chabouté V, Peter P, Henon Ph
Département d'Hématologie Centre Hospitalier de Mulhouse Mulhouse France.
Cytotherapy. 2004;6(6):571-83. doi: 10.1080/14653240410011918.
We and others have shown a critical role for CD34+ CD38- cells in hematopoietic recovery after autologous stem cell transplantation (ASCT), in particular for platelet reconstitution. Thus a routine assessment of CD34+ CD38- cells in freezing-thawing procedures for autografting could represent an important tool for predicting poor engraftment.
To compare the impact of cryopreservation on CD34+ CD38+ and CD34+ CD38- hematopoietic stem cell subsets, 193 autograft products collected in 84 patients with malignancies were assessed before controlled-rate cryopreservation in 10% DMSO and after thawing for autografting.
Cell counts after thawing were significantly different from the pre-freezing counts for total CD34+ (P<0.0001) and CD34+ CD38+ (P<0.0001) cells, but not for CD34+ CD38- cells (P=0.252). Median losses for CD34+, CD34+ CD38+ and CD34+ CD38- cells were, respectively, 11.8%, 11.4% and 0.0%. The magnitude of fresh/post-thawing percentage cell variation was significantly different when comparing between the CD34+ CD38+ and CD34+ CD38- cell subsets (P<0.001). Moreover, CD34+ CD38- cells exhibited recovery values > or =100% in 85/160 graft products, compared with 51/193 in CD34+ CD38+ cells (P<0.0001). Also, recovery values > or =90% were significantly better in the CD34+ CD38- (98/160 grafts) than in the CD34+ CD38+ subsets (89/193 grafts) (P<0.01).
In this work we have demonstrated that CD34+ cells that do not express the CD38 Ag show a significantly better resistance to cryopreservation. This could represent another example of the particular ability of less committed progenitor cells to overcome environmental injuries. Moreover, we consider routine assessment of CD34+ CD38- cells before freezing as clinically relevant, but post-thawing controls may be avoided because of their good resistance to freezing.
我们和其他研究人员已表明,CD34+ CD38-细胞在自体干细胞移植(ASCT)后的造血恢复中起关键作用,尤其是在血小板重建方面。因此,在自体移植的冻融过程中对CD34+ CD38-细胞进行常规评估可能是预测植入不良的重要工具。
为比较冷冻保存对CD34+ CD38+和CD34+ CD38-造血干细胞亚群的影响,对84例恶性肿瘤患者收集的193份自体移植产品在10%二甲基亚砜中进行程序降温冷冻保存前及解冻后用于自体移植时进行评估。
解冻后的细胞计数与冷冻前总CD34+细胞(P<0.0001)和CD34+ CD38+细胞(P<0.0001)的计数有显著差异,但与CD34+ CD38-细胞的计数无显著差异(P=0.252)。CD34+、CD34+ CD38+和CD34+ CD38-细胞的中位损失分别为11.8%、11.4%和0.0%。比较CD34+ CD38+和CD34+ CD38-细胞亚群时,新鲜/解冻后细胞百分比变化幅度有显著差异(P<0.001)。此外,在160份移植产品中,85份CD34+ CD38-细胞的恢复值≥100%,而CD34+ CD38+细胞为51/193(P<0.0001)。同样,CD34+ CD38-细胞亚群中恢复值≥90%的情况(98/160份移植)明显优于CD34+ CD38+亚群(89/193份移植)(P<0.01)。
在本研究中,我们证明不表达CD38抗原的CD34+细胞对冷冻保存的耐受性明显更好。这可能是未定向祖细胞克服环境损伤特殊能力的又一实例。此外,我们认为冷冻前对CD34+ CD38-细胞进行常规评估具有临床相关性,但由于其对冷冻的良好耐受性,解冻后控制可能可避免。