Leger R M, Arndt P A, Ciesielski D J, Garratty G
American Red Cross Blood Services, Southern California Region, Los Angeles, USA.
Transfusion. 1998 Jun;38(6):565-72. doi: 10.1046/j.1537-2995.1998.38698326336.x.
During the use of commercial red cell (RBC) acid-elution kits for adsorption and elution (adsorption/elution) studies with anti-D, unexpected reactive eluates (anti-D) were obtained from D- RBCs. Such results were not obtained with a parallel xylene method or, historically, with heat and ether methods.
Single-donor and commercial polyclonal anti-D samples were incubated with D+ and D- RBCs. Acid eluates were prepared by the manufacturers' directions. Variations in the wash step of the eluate preparation included the use of commercial kit wash solution versus phosphate-buffered saline versus solutions of various ionic strengths.
Anti-D was eluted from 20 of 22 samples of D- RBCs after incubation with commercial polyclonal anti-D (titer 512) and from 2 of 3 samples of D- RBCs incubated with single-donor anti-D (titer 256). With a low-titer (16) single-donor anti-D, 0 of 4 eluates from D- RBCs reacted. When phosphate-buffered saline was substituted for the commercial wash solution, 0 of 11 D- RBC eluates reacted, as compared with 9 of 11 D- RBCs that yielded positive 1+(-)2+ eluates with the commercial wash solution. If the recommended initial phosphate-buffered saline wash was omitted before the use of the commercial wash solution, the eluate reactivity was stronger (2+(-)3+). When low-ionic-strength (< 0.03 M) saline was substituted, anti-D was eluted from D- RBCs. All last washes were nonreactive. Antiglobulin tests on all adsorbing D- were negative.
Commercial wash solutions used for acid elution are at low ionic strength and commonly yield superior eluates, but in the presence of high-titer antibodies, false-positive eluates can result. It is our belief that the low-ionic-strength wash solution caused aggregation of IgG and nonspecific attachment of IgG on RBCs. Aggregates will contain IgG serum antibodies in proportion to the titer of the antibody. It is this nonspecifically bound antibody that is eluted from antigen-negative RBCs.
在使用商业红细胞(RBC)酸洗脱试剂盒进行抗-D吸附和洗脱(吸附/洗脱)研究时,从D-红细胞中获得了意外的反应性洗脱液(抗-D)。采用平行二甲苯法或历史上的加热和乙醚法均未得到此类结果。
将单供体和商业多克隆抗-D样本与D+和D-红细胞一起孵育。按照制造商的说明制备酸洗脱液。洗脱液制备洗涤步骤的变化包括使用商业试剂盒洗涤液、磷酸盐缓冲盐水以及不同离子强度的溶液。
用商业多克隆抗-D(效价512)孵育后,22份D-红细胞样本中有20份洗脱得到抗-D,用单供体抗-D(效价256)孵育的3份D-红细胞样本中有2份洗脱得到抗-D。使用低效价(16)单供体抗-D时,4份D-红细胞洗脱液中无反应。用磷酸盐缓冲盐水替代商业洗涤液时,11份D-红细胞洗脱液中无反应,而使用商业洗涤液时,11份D-红细胞中有9份产生1+(-)2+阳性洗脱液。如果在使用商业洗涤液之前省略推荐的初始磷酸盐缓冲盐水洗涤,洗脱液反应性更强(2+(-)3+)。用低离子强度(<0.03M)盐水替代时,D-红细胞洗脱得到抗-D。所有末次洗涤均无反应。对所有吸附D-的样本进行抗球蛋白试验均为阴性。
用于酸洗脱的商业洗涤液离子强度低,通常能产生优质洗脱液,但在存在高效价抗体的情况下,可能导致假阳性洗脱液。我们认为,低离子强度洗涤液导致IgG聚集以及IgG在红细胞上的非特异性附着。聚集体将按抗体效价比例包含IgG血清抗体。正是这种非特异性结合的抗体从抗原阴性红细胞中被洗脱出来。