Farrugia A, Shea N, Knowles S, Holdsworth R, Piouronowski H, Portbury D, Romeo A
Red Cross Blood Bank, South Melbourne, Australia.
J Clin Pathol. 1993 Aug;46(8):742-5. doi: 10.1136/jcp.46.8.742.
To investigate treatment with glycerol/washing as a potential substitute for freeze-thawing in the production of leucocyte depleted red cell concentrates for patients with a history of non-haemolytic reactions following transfusion.
The standard procedure of treatment with glycerol/-80 degrees C freezing/thawing/washing was compared with a similar procedure in which freezing was omitted. The quality of the resulting red cell products was assessed in relation to: (1) standard red cell biochemical parameters; (2) leucocyte and lymphocyte subset composition using flow cytometry with fluorescent labelled monoclonal antibodies; and (3) immunogenicity of the residual lymphocytes in mixed lymphocyte culture.
Compared with red cells subjected to the standard freeze-thaw technique, red cells undergoing the non-freezing procedure and suspended in additive solutions had significantly better biochemical preservation after 21 days of storage (p < 0.001). Both procedures removed an average 98% of the initial leucocytes at the expense of 18-20% of the red cells. The non-freezing procedure resulted in higher residual concentrations of HLA class II bearing lymphocytes (p < 0.01), but not higher numbers of dendritic cells. Both procedures were equally effective in annulling the residual lymphocytes' ability to act as stimulator cells in one-way mixed lymphocyte culture.
The non-freezing procedure produces a superior product for the provision of red cells to patients with granulocyte antibodies. These products may also offer a lower risk of HLA alloimmunisation to previously unexposed patients.
研究甘油/洗涤处理作为冻融法的潜在替代方法,用于为有输血后非溶血性反应病史的患者制备去白细胞红细胞浓缩液。
将甘油/-80℃冷冻/解冻/洗涤的标准处理程序与省略冷冻步骤的类似程序进行比较。根据以下方面评估所得红细胞产品的质量:(1)标准红细胞生化参数;(2)使用荧光标记单克隆抗体的流式细胞术检测白细胞和淋巴细胞亚群组成;(3)混合淋巴细胞培养中残余淋巴细胞的免疫原性。
与采用标准冻融技术处理的红细胞相比,未进行冷冻处理并悬浮于添加剂溶液中的红细胞在储存21天后生化保存效果显著更好(p < 0.001)。两种程序平均去除了98%的初始白细胞,但红细胞损失了18 - 20%。非冷冻程序导致携带HLA II类分子的淋巴细胞残余浓度更高(p < 0.01),但树突状细胞数量未增加。两种程序在消除残余淋巴细胞在单向混合淋巴细胞培养中作为刺激细胞的能力方面同样有效。
对于向有粒细胞抗体的患者提供红细胞而言,非冷冻程序产生的产品更优。这些产品对先前未接触过的患者而言,发生HLA同种免疫的风险可能也更低。