血液病患者原发性和持续性血小板输注难治性抗hla - c自身抗体的存在及其意义:一项来自单一中心的回顾性研究

Annals of medicine Pub Date : 2025-12-01 Epub Date: 2024-12-28 DOI:10.1080/07853890.2024.2446689
Xunhua Li, Qi Liu, Jingjie Dong, Yaonan Hong, Chuanao Xin, Junfeng Guo, Shan Liu, Peicheng Wang, Zexing Sun, Yingying Shen, Xiawan Yang, Hangchao Li, Yiping Shen, Jianping Shen, Baodong Ye, Yuhong Zhou, Tonglin Hu, Dijiong Wu
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引用次数: 0

摘要

目的:血小板输注难治性(PTR)是一个令人沮丧的临床问题,原发性和持续性(P/P) PTR未能很好地认识到自第一次输注以来发生持续PTR的患者。本研究旨在探讨P/P PTR的发生率及危险因素。方法:回顾2019年1月至2023年3月期间接受HLA高分辨率基因分型和供者特异性HLA抗体或群体反应性抗体(PRA)检测的血液病患者。描述临床资料,包括感染史、脾肿大、输血次数和数量以及输血反应。结果:回顾性分析114例患者,记录1071例输血。PTR总发生率为28.95%(33/114),其中P/P PTR发生率为63.63%(21/33)。多因素logistic回归分析发现抗I类HLA抗体是血小板输注无效的独立危险因素(p = 0.034)。有趣的是,6例患者首次发现抗hla -C自身抗体,1例患者同时检测到抗hla - a和C自身抗体,占HLA-I抗体阳性患者的10.71%(6/56)。进一步分析发现,抗hla - c自身抗体是P/P PTR的独立危险因素(P = 0.039)。在抗hla - c抗体阳性的患者中,有或没有抗hla - c自身抗体的患者在ABO、d匹配和交叉匹配输注的有效性上存在显著差异(p p = 0.017)。值得注意的是,接受利妥昔单抗治疗的4名患者中有2名实现了血小板输注独立性。结论:本工作强调了抗hla - c自身抗体对血液病患者P/P PTR的意义,利妥昔单抗可治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Existence and significance of anti-HLA-C autoantibodies to primary and persistent platelet transfusion refractoriness in patients with hematologic disorders: a retrospective study from a single centre.

Objectives: Platelet transfusion refractoriness (PTR) is a frustrating clinical problem, and primary and persistent (P/P) PTR who experienced persistent PTR since the first transfusion was failed to be well recognized. This study aims to investigate the incidence and risk factors for P/P PTR.

Methods: Patients with hematologic disorders who underwent HLA high-resolution genotyping and donor-specific HLA antibody or panel reactive antibody (PRA) testing between January 2019 and March 2023 were reviewed. Clinical data including infection history, splenomegaly, frequency and quantity of blood transfusions, and transfusions response were delineated and subsequently analyzed.

Results: 114 patients were included retrospectively, and 1071 transfusions were recorded. The overall incidence of PTR was 28.95% (33/114), with 63.63% (21/33) being P/P PTR. Anti class I HLA (anti-HLA-I) antibody was identified as an independent risk factor for ineffective platelet transfusion through multivariate logistic regression analysis (p = .034). Interestingly, anti-HLA-C autoantibodies were first found in six patients, and both anti-HLA-A and C autoantibodies were detected in one case, comprising a total of 10.71% (6/56) of HLA-I antibody-positive patients. Further analysis revealed that anti-HLA-C autoantibody was identified as an independent risk factor for P/P PTR (p = .039). Among patients with positive anti-HLA-C antibodies, significant differences in the effectiveness of ABO, D-matched and cross-matching transfusions were observed between patients with or without anti-HLA-C autoantibodies (p < .001 and p = .017). Notably, platelet transfusions independence was achieved by two of the four patients who received rituximab.

Conclusions: This work emphasized the significance of anti-HLA-C autoantibody for P/P PTR in hematological patients, and rituximab may therapeutic.

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