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深入探究移植后弥漫性大B细胞淋巴瘤的发病机制和基因组学。

Delving deeper into the pathogenesis and genomics of posttransplant diffuse large B-cell lymphoma.

作者信息

Sneyers Flore, Rocha-Iraizos Ana-Lucía, Vergote Vibeke K J, Dierickx Daan

机构信息

Department of Oncology Laboratory of Experimental Hematology KU Leuven Leuven Belgium.

Department of Human Genetics Laboratory of Molecular Biology of Leukemia KU Leuven Leuven Belgium.

出版信息

Hemasphere. 2025 Apr 15;9(4):e70123. doi: 10.1002/hem3.70123. eCollection 2025 Apr.

Abstract

Posttransplant lymphoproliferative disorders (PTLDs) are a well-known complication of solid organ transplantation and allogeneic hematopoietic stem cell transplantation. The diffuse large B-cell lymphoma subtype (PT-DLBCL) is the most frequent monomorphic PTLD and is associated with poor prognosis. Transplant recipients have an increased risk of abnormal proliferation of lymphoid cells because of diminished immune surveillance. In about 60% of the cases, Epstein-Barr virus infection seems to contribute to the cancer phenotype. Although clinical and research interest in the disorder has increased during the last two decades, the pathology of the disease remains largely elusive. In this review, we summarize current knowledge of PT-DLBCL pathogenesis, and we discuss how a better understanding of PT-DLBCL can lead to improved diagnostics and therapeutic strategies.

摘要

移植后淋巴细胞增生性疾病(PTLD)是实体器官移植和异基因造血干细胞移植的一种常见并发症。弥漫性大B细胞淋巴瘤亚型(PT-DLBCL)是最常见的单形性PTLD,且预后不良。由于免疫监视功能减弱,移植受者发生淋巴细胞异常增殖的风险增加。在约60%的病例中,爱泼斯坦-巴尔病毒感染似乎促成了癌症表型。尽管在过去二十年中,对该疾病的临床和研究兴趣有所增加,但其病理学在很大程度上仍不清楚。在本综述中,我们总结了PT-DLBCL发病机制的现有知识,并讨论了对PT-DLBCL的更好理解如何能够带来改进的诊断和治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5401/11997454/54606698851d/HEM3-9-e70123-g001.jpg

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