Pereira A, Mazzara R, Gelabert A, Castillo R
Department of Hemotherapy and Hemostasis, Hospital Clinico, Barcelona, Spain.
Haematologica. 1991 Nov-Dec;76(6):475-8.
The screening for unexpected antibodies has proved to be a suitable pretransfusion compatibility method, but controversy still remains regarding the most appropriate serologic techniques to use in such a screening and, in particular, whether or not to use enzyme-based methods.
Over a period of three years, 27,149 patient sera submitted to pretransfusion testing were screened for unexpected antibodies. Serologic techniques included LISS-direct agglutination (DAG) reading plus indirect antiglobulin test (IAT), and two-stage papain (2SP)-IAT.
In all, 592 (2.18%) serum samples yielded a positive result. Further studies of these specimens disclosed 466 alloantibodies in 371 cases, and 221 unwanted positive reactivities. 2SP-IAT and LISS-DAG allowed the detection of 124 alloantibodies missed by LISS-IAT (78 anti-Lewis, 33 anti-E, 7 anti-P1, 2 anti-K1, 2 anti-K3, 1 anti-M, 1 anti-Cw), but were responsible for 81% of the unwanted positive reactivities.
Since most alloantibodies detected only by 2SP-IAT or LISS-DAG were of doubtful clinical significance, and these techniques produced a high number of unwanted positive reactivities, we conclude that 2SP-IAT and LISS-DAG are not appropriate for the pretransfusion screening for unexpected antibodies.
意外抗体筛查已被证明是一种合适的输血前相容性检测方法,但对于此类筛查中最适宜采用的血清学技术,尤其是是否使用基于酶的方法,仍存在争议。
在三年时间里,对27149份用于输血前检测的患者血清进行意外抗体筛查。血清学技术包括低离子强度溶液-直接凝集(DAG)读数加间接抗球蛋白试验(IAT),以及两阶段木瓜蛋白酶(2SP)-IAT。
总计592份(2.18%)血清样本检测结果呈阳性。对这些样本的进一步研究发现,371例中有466种同种抗体,以及221种不必要的阳性反应。2SP-IAT和低离子强度溶液-直接凝集检测出低离子强度溶液-IAT漏检的124种同种抗体(78种抗刘易斯抗体、33种抗-E抗体、7种抗-P1抗体、2种抗-K1抗体、2种抗-K3抗体、1种抗-M抗体、1种抗-Cw抗体),但产生了81%的不必要阳性反应。
由于大多数仅通过2SP-IAT或低离子强度溶液-直接凝集检测出的同种抗体临床意义存疑,且这些技术产生了大量不必要的阳性反应,我们得出结论,2SP-IAT和低离子强度溶液-直接凝集不适用于输血前意外抗体筛查。