旅客淋巴细胞综合征——流行病学、发病机制、诊断、治疗及未来发展方向综述。

0 MEDICINE, RESEARCH & EXPERIMENTAL
Yingfang Pan, Aiping Zhao, Xiujiao Jiang, Na Zhou, Jing Wang, Changkui Sun, Fang Zhou
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引用次数: 0

摘要

乘客淋巴细胞综合征(PLS)是移植后可能发生的一种血液学并发症,其特征是供体来源的记忆B淋巴细胞产生针对受体血细胞的抗体。本文综述了PLS的病理生理学、诊断方法和治疗策略,旨在加强临床管理和规范治疗方案。通过Web of Science和PubMed进行文献检索,以确定PLS的相关出版物,共发现79项研究。研究是根据预先确定的标准选择的,包括关注人类供体来源的同种免疫,记录的血型抗原-抗体相互作用,移植背景,结果或管理的临床数据,以及方法有效性。仅包含实际患者数据和关于PLS的实质性讨论的研究被纳入。PLS通常表现为溶血性贫血,伴有乳酸脱氢酶(LDH)水平升高,间接高胆红素血症和触珠蛋白水平降低。诊断主要基于临床表现和实验室检查,包括直接抗球蛋白试验(DAT)和抗体筛选。鉴别诊断对于排除药物性溶血性贫血和血栓性微血管病变至关重要。目前对PLS的治疗策略侧重于停止溶血和恢复血液平衡。一线治疗包括供体相容的红细胞输注和大剂量皮质类固醇,而难治性病例可能需要美罗华或血浆置换。尽管PLS管理取得了进步,但挑战仍然存在,包括由于自限性病例和缺乏标准化治疗方案而导致的诊断延迟。未来的研究应纳入基因组学和蛋白质组学生物标志物,以准确诊断和预测风险。开发针对供体淋巴细胞的机制驱动疗法和建立全球共识框架可以加强监测,提高移植物存活率,并优化移植受体的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Passenger lymphocyte syndrome - Epidemiology, pathogenesis, diagnosis, treatment and future directions: A review.

Passenger lymphocyte syndrome - Epidemiology, pathogenesis, diagnosis, treatment and future directions: A review.

Passenger lymphocyte syndrome - Epidemiology, pathogenesis, diagnosis, treatment and future directions: A review.

Passenger lymphocyte syndrome - Epidemiology, pathogenesis, diagnosis, treatment and future directions: A review.

Passenger lymphocyte syndrome (PLS) is a hematological complication that can occur following transplantation, characterized by donor-derived memory B lymphocytes producing antibodies against the recipient's blood cells. This review examines the pathophysiology, diagnostic approaches, and treatment strategies aimed at enhancing clinical management and standardizing therapeutic protocols for PLS. A literature search was conducted using Web of Science and PubMed to identify relevant publications on PLS, resulting in 79 studies. Studies were selected based on predefined criteria, including a focus on human donor-derived alloimmunity, documented blood group antigen-antibody interactions, transplantation context, clinical data on outcomes or management, and methodological validity. Only studies containing actual patient data and substantive discussions about PLS were included. PLS commonly presents as hemolytic anemia, accompanied by elevated lactate dehydrogenase (LDH) levels, indirect hyperbilirubinemia, and reduced haptoglobin levels. Diagnosis is primarily based on clinical manifestations and laboratory tests, including the direct antiglobulin test (DAT) and antibody screening. Differential diagnosis is crucial for excluding drug-induced hemolytic anemia and thrombotic microangiopathy. Current treatment strategies for PLS focus on halting hemolysis and restoring hematological balance. First-line treatment includes donor-compatible red blood cell transfusions and high-dose corticosteroids, while refractory cases may necessitate rituximab or plasmapheresis. Despite advancements in PLS management, challenges persist, including delayed diagnosis due to self-limiting cases and a lack of standardized treatment protocols. Future research should incorporate genomic and proteomic biomarkers for accurate diagnosis and risk prediction. Developing mechanism-driven therapies targeting donor lymphocytes and establishing global consensus frameworks can enhance monitoring, improve graft survival, and optimize transplant recipient outcomes.

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