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异基因干细胞移植后的内皮功能障碍综合征

Endothelial Dysfunction Syndromes after Allogeneic Stem Cell Transplantation.

作者信息

Vythoulkas Dionysios, Tsirigotis Panagiotis, Griniezaki Marianna, Konstantellos Ioannis, Lazana Ioanna

机构信息

2nd Department of Internal Medicine, Propaedeutic, ATTIKO General University Hospital, National and Kapodistrian University of Athens, Rimini-1, Haidari, 12462 Athens, Greece.

出版信息

Cancers (Basel). 2023 Jan 22;15(3):680. doi: 10.3390/cancers15030680.

Abstract

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the only therapy with a curative potential for a variety of malignant and non-malignant diseases. The major limitation of the procedure is the significant morbidity and mortality mainly associated with the development of graft versus host disease (GVHD) as well as with a series of complications related to endothelial injury, such as sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD), transplant-associated thrombotic microangiopathy (TA-TMA), etc. Endothelial cells (ECs) are key players in the maintenance of vascular homeostasis and during allo-HSCT are confronted by multiple challenges, such as the toxicity from conditioning, the administration of calcineurin inhibitors, the immunosuppression associated infections, and the donor alloreactivity against host tissues. The early diagnosis of endothelial dysfunction syndromes is of paramount importance for the development of effective prophylactic and therapeutic strategies. There is an urgent need for the better understanding of the pathogenetic mechanisms as well as for the identification of novel biomarkers for the early diagnosis of endothelial damage. This review summarizes the current knowledge on the biology of the endothelial dysfunction syndromes after allo-HSCT, along with the respective therapeutic approaches, and discusses the strengths and weaknesses of possible biomarkers of endothelial damage and dysfunction.

摘要

异基因造血干细胞移植(allo-HSCT)仍然是唯一对多种恶性和非恶性疾病具有治愈潜力的疗法。该手术的主要局限性在于其显著的发病率和死亡率,主要与移植物抗宿主病(GVHD)的发生以及一系列与内皮损伤相关的并发症有关,如肝窦阻塞综合征/静脉闭塞性疾病(SOS/VOD)、移植相关血栓性微血管病(TA-TMA)等。内皮细胞(ECs)是维持血管稳态的关键因素,在allo-HSCT过程中面临多种挑战,如预处理的毒性、钙调神经磷酸酶抑制剂的使用、免疫抑制相关感染以及供体对宿主组织的同种异体反应性。内皮功能障碍综合征的早期诊断对于制定有效的预防和治疗策略至关重要。迫切需要更好地了解发病机制,并识别用于早期诊断内皮损伤的新型生物标志物。本综述总结了目前关于allo-HSCT后内皮功能障碍综合征生物学的知识,以及相应的治疗方法,并讨论了内皮损伤和功能障碍可能的生物标志物的优缺点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb92/9913851/7a88d6e49f57/cancers-15-00680-g001.jpg

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