Hyun Jungwon, Lim Young Mi, Park Kyung Deuk, Han Bok Youn, Kim Yang Hyun, Han Kyou Sup, Park Myoung Hee
Department of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Korean J Lab Med. 2009 Oct;29(5):481-9. doi: 10.3343/kjlm.2009.29.5.481.
Majority of immune-mediated platelet refractoriness is caused by HLA alloimmunization and can be effectively managed by HLA-matched platelet transfusions. However, HLA class I-typed large-sized donor registry has not been well established in Korea. We evaluated the effectiveness of platelet transfusion using HLA crossmatch-compatible donors without HLA typing.
Sixteen patients showing platelet refractoriness to random donor platelets (1 hr corrected count increment [CCI] <7,500/microL/m(2)) and HLA alloimmunization (class I panel reactive antibody >60%) were crossmatched with 78 platelet apheresis-eligible donors using National Institute of Health (NIH) and anti-human globulin (AHG) lymphocytotoxicity methods. NIH negative/AHG negative and NIH negative/AHG positive donors were selected as best and second choice donors, respectively.
Eleven patients (11/16, 69%) could find NIH-crossmatch negative donors and 27 donors (27/78, 35%) belonged to the best donors. To 8 patients, 32 apheresis platelet products from 19 donors were transfused. The mean 1 hr and 24 hr CCI values from the best donors were significantly higher than those from random donors (17,893 vs 2,358, P=0.003; 8,292 vs -614, P<0.001), whereas such differences were not observed for those from the second choice donors. Platelet storage time was inversely correlated with CCI values and platelets stored < or =10 hr after collection gave significantly higher CCI values. Neither ABO match nor donor status (related vs unrelated) affected the transfusion effectiveness.
Effective post-transfusion platelet increment using HLA crossmatch-compatible donors was attained in patients with platelet refractoriness due to HLA antibodies, and this method can be used effectively where HLA-typed platelet donor registry is not available.
大多数免疫介导的血小板输注无效是由人类白细胞抗原(HLA)同种免疫引起的,可通过输注HLA匹配的血小板有效处理。然而,韩国尚未建立完善的HLA I类分型大型供者登记系统。我们评估了使用未经HLA分型但HLA交叉配型相容的供者进行血小板输注的有效性。
16例对随机供者血小板输注无效(1小时校正计数增加值[CCI]<7500/μL/m²)且存在HLA同种免疫(I类板反应性抗体>60%)的患者,采用美国国立卫生研究院(NIH)和抗人球蛋白(AHG)淋巴细胞毒性方法,与78例符合血小板单采条件的供者进行交叉配型。分别选择NIH阴性/AHG阴性和NIH阴性/AHG阳性供者作为最佳和次选供者。
11例患者(11/16,69%)能够找到NIH交叉配型阴性的供者,27例供者(27/78,35%)属于最佳供者。对8例患者输注了来自19例供者的32个单采血小板制品。最佳供者的平均1小时和24小时CCI值显著高于随机供者(17893对2358,P=0.003;8292对-614,P<0.001),而次选供者则未观察到这种差异。血小板储存时间与CCI值呈负相关,采集后储存≤10小时的血小板CCI值显著更高。ABO血型匹配和供者状态(亲属供者与非亲属供者)均不影响输注效果。
对于因HLA抗体导致血小板输注无效的患者,使用HLA交叉配型相容的供者可有效提高输血后血小板增加值,在没有HLA分型血小板供者登记系统的情况下,该方法可有效应用。