Calonego Soraia B, Barjas-Castro Maria de Lourdes, Metze Konradin, Pereira Fernanda G, Lorand-Metze Irene
Department of Internal Medicine, Faculty of Medicine, State University of Campinas, Rua Tessália Vieira de Carvalho 126, São Paulo, Brazil.
Transfus Apher Sci. 2008 Apr;38(2):101-7. doi: 10.1016/j.transci.2007.11.001. Epub 2008 Mar 11.
Red blood cell (RBC) antigens may present changes in density during storage and leukocyte reduction. We evaluated the influence of these variables on FY1, FY2, MNS3 and MNS4 antigens using quantitative flow cytometry (FCM). Forty-eight RBC units were divided into two sub-units each immediately after collection. One of them was leukocyte reduced before storage. Antigen expression was analyzed on days 1 and 35 of storage by gel-centrifugation and FCM. Three RBC samples were submitted to papain and bromelin treatment. The gel-centrifugation test could not detect any influence of storage or leukocyte reduction. However, by FCM, a wide variation of antigen density among the donors was found. Leukocyte depletion did not change the antigen density but after storage, expression of FY1 and MNS4 showed a slight decrease. Median antigenic density of FY1 was 11,332 in FY1,2 and 23,436 in FY1,-2 donors. FY2 presented 7204 and 7868, respectively. MNS4 had 100,589 and 214,340 sites in donors MNS3,4 and MNS-3,4, respectively, and MNS3 had 10,389 and 21,122 sites, respectively. After enzyme treatments none of the antigens could be detected. FCM was a reproducible technique, suitable for the quantification of the antigens studied in RBC concentrates stored and leukocyte reduced in conditions normally used for blood transfusion.
红细胞(RBC)抗原在储存和白细胞去除过程中可能会出现密度变化。我们使用定量流式细胞术(FCM)评估了这些变量对FY1、FY2、MNS3和MNS4抗原的影响。48个红细胞单位在采集后立即各分为两个亚单位。其中一个在储存前进行白细胞去除。在储存的第1天和第35天通过凝胶离心和FCM分析抗原表达。对三个红细胞样本进行木瓜蛋白酶和菠萝蛋白酶处理。凝胶离心试验未检测到储存或白细胞去除的任何影响。然而,通过FCM发现供体之间抗原密度存在很大差异。白细胞去除并未改变抗原密度,但储存后,FY1和MNS4的表达略有下降。FY1,2供体中FY1的中位抗原密度为11,332,FY1,-2供体中为23,436。FY2分别为7204和7868。MNS4在MNS3,4和MNS-3,4供体中分别有100,589和214,340个位点,MNS3分别有10,389和21,122个位点。酶处理后未检测到任何抗原。FCM是一种可重复的技术,适用于定量在通常用于输血的条件下储存和白细胞去除的红细胞浓缩物中所研究的抗原。