Investigating discrepancies and false positives in immunohematology tests using gel cards: insights from a case study on antibodies targeting the gel card matrix.

IF 1
Deerej P, Revathy R Menon, Somnath Mukherjee, Satya Prakash, Ansuman Sahu, Debasish Mishra
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Abstract

Introduction: Discrepancies in gel card immunohematologic testing can result in false-positive reactions, making detecting antibodies and performing crossmatching difficult. Such unexpected reactivity may result from interactions with test system components, including the column matrix, chemicals, or reagents, rather than true antigen-antibody binding. Accurate identification and resolution of these discrepancies are crucial to prevent delays in transfusion and ensure patient safety.

Methods: This case involved a 24-year-old patient with sickle cell disease who required a blood transfusion, highlighting the diagnostic challenges posed by variability in gel card platforms. Blood grouping was performed using Tulip gel cards (Tulip Diagnostics, Pvt Ltd).

Results: The forward grouping was AB positive, but the reverse grouping showed pan-positive results. Repeat grouping by the gold standard-the conventional tube technique-resolved the discrepancy, and the blood group was identified as AB positive. Antibody screening (ABS) and autoantibody testing using Tulip gel cards showed pan-positive reactions, although the direct antiglobulin test was negative. However, conventional tube techniques for ABS and thermal amplitude tests for autoantibodies were negative. Crossmatching of phenotype-matched packed red blood cell units showed incompatibility on Tulip gel cards but compatibility using the conventional tube technique. The possibility of antibodies against enhancement media, such as low-ionic-strength solution, was ruled out after repeat testing with normal saline and phosphate-buffered saline, which showed negative reactions in different immunohematology tests. Due to suspected interference from the gel card components, crossmatching, ABS, and autoantibody testing were repeated using Bio-Rad gel cards, which showed compatible results.

Discussion: The false-positive reactions were attributed to antibodies against materials in Tulip gel cards, including silica-based microbeads, polyvinyl alcohol, and other stabilizers that are absent in Bio-Rad gel cards. This case underscores the importance of multiplatform validation, reagent standardization, and conventional tube testing in resolving immunohematologic discrepancies and ensuring safe transfusion practices.

使用凝胶卡调查免疫血液学测试中的差异和假阳性:来自针对凝胶卡矩阵的抗体案例研究的见解。
凝胶卡免疫血液学检测的差异可能导致假阳性反应,使检测抗体和进行交叉匹配变得困难。这种意想不到的反应性可能是由于与测试系统组件的相互作用,包括柱基质、化学物质或试剂,而不是真正的抗原-抗体结合。准确识别和解决这些差异对于防止输血延误和确保患者安全至关重要。方法:该病例涉及一名需要输血的24岁镰状细胞病患者,突出了凝胶卡平台的可变性所带来的诊断挑战。使用Tulip凝胶卡(Tulip Diagnostics, Pvt Ltd)进行血型分型。结果:正向组为AB阳性,反向组为泛阳性。重复分组金标准-传统的试管技术-解决了差异,血型被确定为AB阳性。抗体筛选(ABS)和使用Tulip凝胶卡的自身抗体检测显示泛阳性反应,尽管直接抗球蛋白试验为阴性。然而,常规的ABS试管技术和自身抗体的热振幅测试均为阴性。表型匹配的填充红细胞单位在郁金香凝胶卡上交叉配型不相容,但在常规试管技术上配型相容。经生理盐水和磷酸盐缓冲盐水反复检测,不同免疫血液学试验均呈阴性反应,排除对低离子强度溶液等增强介质产生抗体的可能性。由于怀疑受到凝胶卡组件的干扰,使用Bio-Rad凝胶卡重复交叉匹配、ABS和自身抗体测试,结果一致。讨论:假阳性反应归因于Tulip凝胶卡中材料的抗体,包括硅基微珠、聚乙烯醇和Bio-Rad凝胶卡中不存在的其他稳定剂。该病例强调了多平台验证、试剂标准化和常规试管检测在解决免疫血液学差异和确保安全输血实践中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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