Mitigating the Prozone-Like Effect in HLA Antibody Testing: A Case Report of Therapeutic Plasma Exchange for Antibody-Mediated Rejection Post-Heart Transplantation

IF 1.4 4区 医学 Q4 HEMATOLOGY Journal of Clinical Apheresis Pub Date : 2024-09-18 DOI:10.1002/jca.22144
Sarah K. Grewal, Robert Achram, Hirotomo Nakahara, John D. Roback, Anna B. Morris, Howard M. Gebel, Robert A. Bray, H. Cliff Sullivan
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Abstract

Therapeutic plasma exchange (TPE) is a cornerstone treatment for antibody-mediated rejection (AMR) post-organ transplantation, aiming to eliminate pathogenic donor-specific HLA antibodies (DSA). However, limitations in HLA antibody interpretation due to the prozone-like effect (PLE) can lead to inaccurate assessment of treatment efficacy. We present a case of a heart transplant recipient with suspected AMR, where an unexpected increase in DSA levels post-TPE prompted investigation into PLE. Solid-phase Luminex assays were employed to detect HLA antibodies. Serum was run neat as well as after treatment with ethylenediaminetetraacetic acid (EDTA). Nephelometry was used to detect complement levels. Laboratory analysis of pre-TPE serum revealed higher DSA levels with EDTA treatment, characteristic of PLE. Complement measurements supported complement-mediated interference in the pre-TPE sample. This case underscores the importance of being aware that PLE can occur in HLA testing and can impact the interpretation of TPE efficacy for AMR.

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减轻 HLA 抗体检测中的 "类区效应":治疗性血浆置换治疗心移植术后抗体介导的排斥反应的病例报告
治疗性血浆置换(TPE)是治疗器官移植后抗体介导排斥反应(AMR)的基础疗法,旨在消除致病性供体特异性 HLA 抗体(DSA)。然而,原区样效应(PLE)对 HLA 抗体判读的限制会导致疗效评估不准确。我们介绍了一例疑似 AMR 的心脏移植受者,TPE 后 DSA 水平的意外升高促使我们对 PLE 进行调查。采用固相 Luminex 检测法检测 HLA 抗体。检测血清的纯度以及乙二胺四乙酸(EDTA)处理后的纯度。使用尼泊金测定法检测补体水平。对 TPE 前血清的实验室分析表明,EDTA 处理后的 DSA 水平更高,这是 PLE 的特征。补体测量结果表明,TPE 前样本中存在补体介导的干扰。该病例强调了意识到 PLE 可能发生在 HLA 检测中的重要性,并可能影响对 AMR 的 TPE 疗效的解释。
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来源期刊
CiteScore
2.80
自引率
13.30%
发文量
70
审稿时长
>12 weeks
期刊介绍: The Journal of Clinical Apheresis publishes articles dealing with all aspects of hemapheresis. Articles welcomed for review include those reporting basic research and clinical applications of therapeutic plasma exchange, therapeutic cytapheresis, therapeutic absorption, blood component collection and transfusion, donor recruitment and safety, administration of hemapheresis centers, and innovative applications of hemapheresis technology. Experimental studies, clinical trials, case reports, and concise reviews will be welcomed.
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