Siani Brigitte, Willimann Katharina, Wymann Sandra, Marques Antunes Adriano, Widmer Eleonora
Biochemical Quality Control, Berne, Switzerland.
Product Development, CSL Behring AG, Berne, Switzerland.
Transfusion. 2015 Jul;55 Suppl 2:S95-7. doi: 10.1111/trf.13095.
Hemolysis reaction is a rare class effect of therapy with intravenously administered human normal immunoglobulin (IVIG). Anti-A/B isoagglutinins (isohemagglutinins) originating from donor plasma are considered a probable risk factor for hemolysis. We hypothesized that screening and exclusion of plasma obtained from donors with high isoagglutinin titers from the manufacturing process would produce a meaningful reduction of anti-A/B isoagglutinin titers of the final IVIG product.
A donor screening method for anti-A isoagglutinins using an automated indirect agglutination test (IAT) in gel cards was developed. Industry-scale donor plasma pools and final IVIG product were prepared according to the manufacturing process of Privigen (human 10% liquid IVIG). Anti-A/B isoagglutinin levels were measured by IAT, direct agglutination test, and a flow cytometry-based assay.
Screening of plasma from 705 randomly selected donors identified 6.8% donors with high anti-A isoagglutinin titers in plasma. Exclusion of plasma from these donors resulted in a one-titer-step reduction of anti-A isoagglutinin in laboratory-scale pooled plasma. The same donor screening method applied to industry-scale production resulted in exclusion of 5.1% of donors and produced a one-titer-step reduction of both anti-A and anti-B isoagglutinin titers in the final IVIG product.
Anti-A/B isoagglutinin titers in IVIG products can be reduced on an industrial scale through implementation of anti-A donor screening, which may lower the risk of hemolysis after IVIG therapy.
溶血反应是静脉注射人正常免疫球蛋白(IVIG)治疗中罕见的类效应。源自供体血浆的抗A/B同种凝集素(同种血凝素)被认为是溶血的一个可能危险因素。我们假设,在生产过程中筛选并排除来自高同种凝集素滴度供体的血浆,将使最终IVIG产品的抗A/B同种凝集素滴度显著降低。
开发了一种使用凝胶卡自动间接凝集试验(IAT)检测抗A同种凝集素的供体筛选方法。根据Privigen(人10%液体IVIG)的生产工艺制备工业规模的供体血浆库和最终IVIG产品。通过IAT、直接凝集试验和基于流式细胞术的检测方法测定抗A/B同种凝集素水平。
对705名随机选择的供体的血浆进行筛选,发现6.8%的供体血浆中抗A同种凝集素滴度高。排除这些供体的血浆后,实验室规模的混合血浆中抗A同种凝集素降低了一个滴度级别。将相同的供体筛选方法应用于工业规模生产,排除了5.1%的供体,并使最终IVIG产品中的抗A和抗B同种凝集素滴度均降低了一个滴度级别。
通过实施抗A供体筛选,可在工业规模上降低IVIG产品中的抗A/B同种凝集素滴度,这可能降低IVIG治疗后溶血的风险。