Makarovska-Bojadzieva Tatjana, Velkova Emilija, Blagoevska Milenka
Institute of Transfusion Medicine, Skopje, Republic of Macedonia.
Open Access Maced J Med Sci. 2017 Apr 8;5(2):107-111. doi: 10.3889/oamjms.2017.054. eCollection 2017 Apr 15.
Red blood cell (RBC) alloimmunization is still an actual problem in our transfusion practice. In 2011, in addition to the regular ABO/D blood group typing, phenotyping for Rh (C, c, E, e) and Kell antigens was introduced for blood donors and patients undergoing blood transfusion. Our aim was to evaluate the impact of the extended RBC typing and donor/recipient matching on the incidence of RBC alloimmunization.
A retrospective comparative study was conducted by reviewing RBC request records for about 36,000 patients transfused with RBC in the period from 2013 to 2015 in comparison to the similar study conducted on 47,000 transfused patients in the period from 2005 to 2008. Pre-transfusion serologic testing data were retrieved for analysis. Blood samples with positive antibody screening and positive cross-match were further subjected to antibody identification. All the tests were performed using column agglutination technique (CAT) with ID-cards and reagents from DiaMed in both studies.
Irregular RBC alloantibodies were detected in 116 (0.32%) out of 36,000 transfused patients. Multiple transfusions (15.8 units/patient) were given to 450 patients from which 79 (17.5%) had RBC allontibodies. The incidence of RBC alloimmunisation in the rest of the 35,550 transfused patients from which 37 had RBC alloantibodies was 0.10%. A total of 117 alloantibodies were identified in 96 out of the 116 patients with irregular RBC antibodies. Their specificity was as fallows: anti-E (25.6%), -C (6.0%), -c (8.5%), -e (0.85%), -C (5.1%), -K (12.8%), -Fy (10.2%), -Fy (2.5%), -Jk (7.7%), -Jk (2.5%), -M (9.4%), -S (1.7%), -s (0.85%), -Lu (1.7%), -Le (3.4%) and anti-Le (0.85%). Multiple antibodies were identified in 22 of the transfused patients out of which 15 (68.2%) received multiple transfusions. Anti-E was the most common antibody found in more of the 50% of the multiple antibody cases.
The overall incidence of RBC alloimmunization in transfused patients decreased from 0.51% which was the estimated incidence for the period before the introduction of the extended RBC typing (2005-2008) to 0.32% (2013-2015). This is due to the decreased incidence of RBC alloimmunization in the multiply transfused patients from 33.9% to 17.5% respectively. The current frequency of anti-E (25.6%) and -K (12.8%) antibodies in transfused patients are significantly lower than their previous estimated frequencies of 30.4% and 24.0% respectively, as well as the overall frequency of RBC antibodies to Rh+Kell antigens which decreased from 72.4% to 53.8%. Extended donor-recipient matching for C, c, E, e and Kell antigens has proved a beneficial effect on the incidence of RBC alloimmunization in multiply transfused patients.
红细胞(RBC)同种免疫在我们的输血实践中仍然是一个现实问题。2011年,除了常规的ABO/D血型分型外,还对献血者和接受输血的患者进行了Rh(C、c、E、e)和Kell抗原的表型分析。我们的目的是评估扩展的红细胞分型和供体/受体匹配对红细胞同种免疫发生率的影响。
进行了一项回顾性比较研究,回顾了2013年至2015年期间约36000例接受红细胞输血的患者的红细胞需求记录,并与2005年至2008年期间对47000例输血患者进行的类似研究进行比较。检索输血前血清学检测数据进行分析。对抗体筛查阳性和交叉配血阳性的血样进一步进行抗体鉴定。在两项研究中,所有检测均使用DiaMed的柱凝集技术(CAT)和身份证及试剂进行。
在36000例输血患者中,有116例(0.32%)检测到不规则红细胞同种抗体。450例患者接受了多次输血(平均每人15.8单位),其中79例(17.5%)有红细胞同种抗体。其余35550例输血患者中有37例有红细胞同种抗体,其红细胞同种免疫发生率为0.10%。在116例有不规则红细胞抗体的患者中,有96例共鉴定出117种同种抗体。其特异性如下:抗-E(25.6%)、-C(6.0%)、-c(8.5%)、-e(0.85%)、-C(5.1%)、-K(12.8%)、-Fy(10.2%)、-Fy(2.5%)、-Jk(7.7%)、-Jk(2.5%)、-M(9.4%)、-S(1.7%)、-s(0.85%)、-Lu(1.7%)、-Le(3.4%)和抗-Le(0.85%)。22例输血患者中鉴定出多种抗体,其中15例(68.2%)接受了多次输血。抗-E是在50%以上的多种抗体病例中发现的最常见抗体。
输血患者红细胞同种免疫的总体发生率从引入扩展红细胞分型前(2005 - 2008年)的估计发生率0.51%降至0.32%(2013 - 2015年)。这是由于多次输血患者中红细胞同种免疫的发生率分别从33.9%降至17.5%。目前输血患者中抗-E(25.6%)和抗-K(12.8%)抗体的频率显著低于之前估计的频率30.4%和24.0%,以及红细胞针对Rh + Kell抗原的抗体总体频率从72.4%降至53.8%。对C、c、E、e和Kell抗原进行扩展的供体-受体匹配已证明对多次输血患者的红细胞同种免疫发生率有有益影响。