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常染色体显性高免疫球蛋白E综合征:何时应考虑造血干细胞移植?

Autosomal dominant hyper-IgE syndrome: When hematopoietic stem cell transplantation should be considered?

作者信息

Oikonomopoulou Christina, Goussetis Evgenios

机构信息

Stem Cell Transplant Unit, Aghia Sophia Children's Hospital, Athens, Greece.

出版信息

Pediatr Transplant. 2020 Aug;24(5):e13699. doi: 10.1111/petr.13699. Epub 2020 Jun 4.

Abstract

AD-HIES or Job's syndrome is a primary immunodeficiency, caused by dominant negative mutations in signal transducer and activator of transcription (STAT) 3. The syndrome is characterized by infectious, immunologic, and non-immunologic manifestations and is associated with significant morbidity, mortality, and development of lymphomas. What has not yet been elucidated is the role of HSCT in the disease treatment spectrum. We review published cases of patients with AD-HIES that underwent HSCT and attempt to clarify at what stage HSCT should be considered and what are the complications.

摘要

常染色体显性遗传高IgE综合征(AD-HIES)或乔布综合征是一种原发性免疫缺陷病,由信号转导和转录激活因子(STAT)3的显性负性突变引起。该综合征的特征为感染性、免疫性和非免疫性表现,并伴有显著的发病率、死亡率以及淋巴瘤的发生。尚未阐明的是异基因造血干细胞移植(HSCT)在该疾病治疗中的作用。我们回顾已发表的接受HSCT的AD-HIES患者病例,并试图阐明应在什么阶段考虑进行HSCT以及有哪些并发症。

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