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通过MAIEA试验和免疫印迹法分析CR1(CD35)上的诺普斯血型抗原。

Analysis of Knops blood group antigens on CR1 (CD35) by the MAIEA test and by immunoblotting.

作者信息

Petty A C, Green C A, Poole J, Daniels G L

机构信息

MRC Blood Group Unit, London, UK.

出版信息

Transfus Med. 1997 Mar;7(1):55-62. doi: 10.1046/j.1365-3148.1997.d01-71.x.

Abstract

Kna, McCa, Sla and Yka are red cell antigens of relatively high frequency, located on complement receptor 1 (CR1, CD35). Antibodies to these Knops system antigens are not uncommon. They are not haemolytic and do not reduce the survival of transfused incompatible red cells, but they are a nuisance in transfusion laboratories as they can cause an incompatible crossmatch and must be identified before they can be dismissed as clinically insignificant. Human red cell alloantibodies can be shown to be Knops system antibodies by the monoclonal-antibody-specific immobilization of erythrocyte antigens (MAIEA) test, using murine monoclonal anti-CR1. In addition to confirming that Kna, McCa, Sla and Yka are located on CR1, the MAIEA test was used to confirm that Csa is not on CR1. Red cells of the Helgeson phenotype, the null phenotype of the Knops system by conventional serological methods, have levels of Kna, McCa, Sla and Yka intermediate between those of alpha-chymotrypsin-treated cells (which lack Knops system antigens) and those of positive control cells. Level of expression of Knops system antigens is very variable and intensity of staining of immunoblots probed with monoclonal anti-CR1 correlated with strength of Knops system antigens, as determined by the MAIEA test. In individuals heterozygous for alleles producing different allotypes, separate bands representing each allotype on an immunoblot showed identical intensity of staining, suggesting that the quantity of CR1 on red cells is controlled, at least in part, by a locus independent of CR1. An analysis of CR1 on red cells of individuals who have made Knops system antibodies suggested that the Knops system antigens and the antibodies that detect them are complex and heterogeneous.

摘要

Kna、McCa、Sla和Yka是频率相对较高的红细胞抗原,位于补体受体1(CR1,CD35)上。针对这些诺普斯系统抗原的抗体并不罕见。它们不具有溶血性,也不会缩短输注不相容红细胞的存活时间,但在输血实验室中却是个麻烦,因为它们会导致交叉配血不相容,在被判定为临床无意义之前必须加以识别。使用鼠单克隆抗CR1,通过红细胞抗原的单克隆抗体特异性固定(MAIEA)试验,可以证明人红细胞同种抗体是诺普斯系统抗体。除了证实Kna、McCa、Sla和Yka位于CR1上之外,MAIEA试验还用于证实Csa不在CR1上。通过传统血清学方法确定的诺普斯系统无效表型的赫尔格森表型红细胞,其Kna、McCa、Sla和Yka水平介于α-糜蛋白酶处理的细胞(缺乏诺普斯系统抗原)和阳性对照细胞之间。诺普斯系统抗原的表达水平变化很大,用单克隆抗CR1探测的免疫印迹染色强度与MAIEA试验确定的诺普斯系统抗原强度相关。在产生不同同种异型等位基因的杂合个体中,免疫印迹上代表每种同种异型的单独条带显示出相同的染色强度,这表明红细胞上CR1的数量至少部分受一个独立于CR1的基因座控制。对产生诺普斯系统抗体的个体红细胞上的CR1进行分析表明,诺普斯系统抗原以及检测它们的抗体是复杂且异质的。

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