Glasser L, Huestis D W
Transfusion. 1979 Jan-Feb;19(1):53-6. doi: 10.1046/j.1537-2995.1979.19179160266.x.
Two hours after normal donors were given intravenous dexamethasone, their leukocytes were collected by intermittent flow centrifugation. Neutrophils were tested immediately after collection and following storage at 4 to 6 C for 24, 48, 72 and 96 hours. Tests included total leukocyte and absolute neutrophil counts, plasma glucose concentrations, the percentage of phagocytic neutrophils, the ability of phagocytes to accumulate particles, candidacidal activity, bactericidal capacity and chemotaxis. Total leukocyte and absolute neutrophil counts in the stored suspensions were decreased after 48 hours (p = .005). Plasma glucose levels in the suspensions declined at first, then stabilized at 48 hours of storage probably because of loss of cellular integrity. Chemotaxis, candidacidal activity, phagocytosis and dye exclusion showed statistically significant decreases at 24 hours. Chemotaxis deteriorated rapidly, with a mean 63 per cent functional loss at 48 hours. We conclude that treatment of donors with dexamethasone does not extend the storage limits of granulocyte concentrates used for clinical transfusions. Based on these and our previous observations, unless the storage changes should be shown to be reversible, granulocyte concentrates should probably not be stored more than 24 hours before transfusion.
正常供体静脉注射地塞米松两小时后,通过间歇流动离心法收集其白细胞。收集后立即对中性粒细胞进行检测,并在4至6℃下储存24、48、72和96小时后再次检测。检测项目包括白细胞总数和中性粒细胞绝对值、血浆葡萄糖浓度、吞噬性中性粒细胞百分比、吞噬细胞积累颗粒的能力、杀念珠菌活性、杀菌能力和趋化性。储存48小时后,储存悬液中的白细胞总数和中性粒细胞绝对值下降(p = 0.005)。悬液中的血浆葡萄糖水平起初下降,然后在储存48小时时趋于稳定,这可能是由于细胞完整性丧失所致。趋化性、杀念珠菌活性、吞噬作用和染料排斥在24小时时显示出统计学上的显著下降。趋化性迅速恶化,在48小时时平均功能丧失63%。我们得出结论,用地塞米松治疗供体并不能延长用于临床输血的浓缩粒细胞的储存期限。基于这些以及我们之前的观察结果,除非储存变化被证明是可逆的,否则浓缩粒细胞在输血前储存时间可能不应超过24小时。