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人类红细胞上的I类HLA分子。定量分析及输血效应。

Class I HLA molecules on human erythrocytes. Quantitation and transfusion effects.

作者信息

Everett E T, Kao K J, Scornik J C

出版信息

Transplantation. 1987 Jul;44(1):123-9. doi: 10.1097/00007890-198707000-00025.

DOI:10.1097/00007890-198707000-00025
PMID:3603672
Abstract

HLA class I molecules were quantitated on erythrocytes from individuals expressing either high or low levels of such antigens. Quantitative determinations were accomplished using 125I-labeled Fab fragments of the anti-HLA monoclonal antibody W6/32 in a competitive binding assay. The experimental conditions of the test system were established using red cells from an individual found to express high levels of red cell HLA when examined by flow cytometry. The competitive binding assay met the requirements of ligand specificity and specific binding saturability. Scatchard analysis revealed that there were 1684 +/- 39 (mean +/- SD) HLA molecules/red cell. In two other donors in whom erythrocyte HLA was undetectable by flow cytometry specific binding of the 125I-W6/32 Fab fragments was clearly demonstrated, indicating the presence of HLA on red cells of these donors as well. The number of HLA molecules/red cell was estimated to be between 100 and 200 for these individuals. Thus, in a blood transfusion unit, the number of HLA molecules contributed by the red cells is comparable to that of the leukocytes. Blood highly depleted of leukocytes and platelets and selected from donors with low amounts of red cell HLA was not beneficial (when transfused to selected patients) in that their sensitizing effects were not significantly different from regular blood transfusions. These results show that the amount of HLA antigens on red cells, while low if compared with other cell types, is significant in terms of the absolute antigenic content of blood transfusions. They also show that transfusion of blood units containing HLA antigens in concentrations as low as can be achieved with current technology were not useful in preventing HLA sensitization in patients at risk.

摘要

对表达此类抗原水平高或低的个体的红细胞上的I类人类白细胞抗原(HLA)分子进行了定量分析。使用抗HLA单克隆抗体W6/32的125I标记的Fab片段,通过竞争性结合试验完成定量测定。使用通过流式细胞术检测发现表达高水平红细胞HLA的个体的红细胞建立测试系统的实验条件。竞争性结合试验符合配体特异性和特异性结合饱和性的要求。Scatchard分析显示,每个红细胞有1684±39(平均值±标准差)个HLA分子。在另外两名供体中,通过流式细胞术无法检测到红细胞HLA,但125I-W6/32 Fab片段的特异性结合得到了明确证明,这表明这些供体的红细胞上也存在HLA。估计这些个体每个红细胞的HLA分子数量在100到200之间。因此,在一个输血单位中,红细胞贡献的HLA分子数量与白细胞相当。从红细胞HLA含量低的供体中选择的高度去除白细胞和血小板的血液(当输给选定的患者时)并无益处,因为它们的致敏作用与常规输血没有显著差异。这些结果表明,红细胞上的HLA抗原量虽然与其他细胞类型相比很低,但就输血的绝对抗原含量而言是显著的。它们还表明,输注含有低至当前技术所能达到浓度的HLA抗原的血液单位对预防有风险患者的HLA致敏没有作用。

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