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整合基因分型以实现更准确的Rh(D)抗原表型分析:一项回顾性研究

Integrating Genotyping for More Accurate Rh(D) Antigen Phenotyping: A Retrospective Study.

作者信息

Barouqa Mohammad, Dela Cruz Nestor

机构信息

Department of Pathology, University of South Alabama, Mobile, AL 36688, USA.

出版信息

Medicina (Kaunas). 2025 Apr 5;61(4):670. doi: 10.3390/medicina61040670.

Abstract

The Rh blood group system is highly polymorphic, and accurate classification of Rh(D) variants is critical in transfusion medicine to prevent alloimmunization and optimize blood utilization. Despite the advances in conventional serologic testing, weak and partial Rh(D) phenotypes still remain challenges in Transfusion Medicine practice. The objective is to implement and assess the impact of genotyping in classifying Rh(D) antigen status. We conducted a retrospective study at the University of South Alabama Medical Center and Children and Women's Hospital between 1 January 2023 and 31 December 2024 to assess the impact of genotyping in cases with discrepant Rh(D) typing, Rh(D)-positive patients with anti-Rh(D) antibodies, and neonates with positive weak Rh(D) tests. ABO and Rh(D) antigen typing was performed on 12,994 patients, including 3767 newly tested individuals. Weak Rh(D) testing was performed on newly tested individuals using automated microplate direct agglutination, followed by molecular genotyping. Among the 25 patients with weak or discrepant Rh(D) phenotypes, weak Rh(D) variants were observed in 52% of cases, with Weak Type 2 being the most common, particularly in pediatric (age < 18 years old) patients. Partial Rh(D) phenotypes were identified in 40% of cases, predominantly among Black individuals. Three patients were reclassified as Rh(D)-positive based on genotyping and received 615 Rh(D)-positive RBC units without evidence of alloimmunization, while four patients were confirmed at risk of alloimmunization and remained classified as Rh(D)-negative. Fisher's exact test demonstrated a significant association between ethnicity and Rh(D) classification ( < 0.01), and the McNemar exact test confirmed a significant reclassification of cases from Rh(D)-negative to Rh(D)-positive ( < 0.01). genotyping enhances the accuracy of Rh(D) antigen classification, mitigating alloimmunization risks and the unnecessary use of Rh Immunoglobulin and optimizing blood product utilization. The reclassification of patients to Rh(D)-positive alleviates pressure on Rh(D)-negative blood supplies, particularly during critical shortages. These findings underscore the necessity of integrating molecular testing into routine transfusion medicine practices to improve patient safety and resource management.

摘要

Rh血型系统具有高度多态性,在输血医学中准确分类Rh(D)变异体对于预防同种免疫和优化血液利用至关重要。尽管传统血清学检测取得了进展,但弱和部分Rh(D)表型在输血医学实践中仍然是挑战。目的是实施并评估基因分型在Rh(D)抗原状态分类中的影响。我们于2023年1月1日至2024年12月31日在南阿拉巴马大学医学中心以及儿童与妇女医院进行了一项回顾性研究,以评估基因分型在Rh(D)分型不一致的病例、有抗Rh(D)抗体的Rh(D)阳性患者以及弱Rh(D)检测呈阳性的新生儿中的影响。对12994名患者进行了ABO和Rh(D)抗原分型,其中包括3767名新检测个体。对新检测个体使用自动微孔板直接凝集法进行弱Rh(D)检测,随后进行分子基因分型。在25例具有弱或不一致Rh(D)表型的患者中,52%的病例观察到弱Rh(D)变异体,其中弱2型最为常见,尤其是在儿科(年龄<18岁)患者中。40%的病例鉴定为部分Rh(D)表型,主要见于黑人个体。3例患者根据基因分型重新分类为Rh(D)阳性,并接受了615单位Rh(D)阳性红细胞,没有同种免疫的证据,而4例患者被确认有同种免疫风险,仍分类为Rh(D)阴性。Fisher精确检验显示种族与Rh(D)分类之间存在显著关联(<0.01),McNemar精确检验证实病例从Rh(D)阴性到Rh(D)阳性有显著的重新分类(<0.01)。基因分型提高了Rh(D)抗原分类的准确性,降低了同种免疫风险以及Rh免疫球蛋白的不必要使用,并优化了血液制品的利用。将患者重新分类为Rh(D)阳性减轻了Rh(D)阴性血液供应的压力,特别是在严重短缺期间。这些发现强调了将分子检测纳入常规输血医学实践以提高患者安全性和资源管理的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d3a/12028936/7255190cc437/medicina-61-00670-g001.jpg

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