Current and emerging treatment options for Wiskott-Aldrich syndrome

被引:54
|
作者
Worth, Austen J. J. [1 ]
Thrasher, Adrian J. [2 ]
机构
[1] Great Ormond St Hosp Natl Hlth Serv Trust, Dept Clin Immunol & Bone Marrow Transplantat, London WC1N 1JH, England
[2] UCL Inst Child Hlth, Dept Mol & Cellular Immunol, London WC1N 1EN, England
基金
英国惠康基金;
关键词
allogeneic hematopoietic stem cell transplantation; autoimmunity; gene therapy; primary immunodeficiency; thrombocytopenia; Wiskott Aldrich syndrome; Wiskott Aldrich syndrome protein; X-linked thrombocytopenia; STEM-CELL TRANSPLANTATION; BONE-MARROW-TRANSPLANTATION; X-LINKED THROMBOCYTOPENIA; SYNDROME PROTEIN WASP; FLOW-CYTOMETRIC ANALYSIS; PRIMARY IMMUNODEFICIENCY DISEASES; LONG-TERM SURVIVAL; N-WASP; ACTIN POLYMERIZATION; ARP2/3; COMPLEX;
D O I
10.1586/1744666X.2015.1062366
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Wiskott-Aldrich syndrome is a life-threatening primary immunodeficiency associated with a bleeding tendency, eczema and a high incidence of autoimmunity and malignancy. Stem cell transplantation offers the opportunity of cure for all these complications, and over the past 35 years there has been a remarkable improvement in survival following this treatment. Here, we review advances in management of clinical complications pre- and post-transplant, as well as discuss the morbidity Wiskott-Aldrich syndrome patients experience following treatment. For patients with a poorly matched stem cell donor, recent gene therapy trials demonstrate encouraging results and the potential of low-toxicity therapy for all patients.
引用
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页码:1015 / 1032
页数:18
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