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Current and emerging treatment options for Wiskott–Aldrich syndrome.

Authors :
Worth, Austen JJ
Thrasher, Adrian J
Source :
Expert Review of Clinical Immunology; Sep2015, Vol. 11 Issue 9, p1015-1032, 18p
Publication Year :
2015

Abstract

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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1744666X
Volume :
11
Issue :
9
Database :
Complementary Index
Journal :
Expert Review of Clinical Immunology
Publication Type :
Academic Journal
Accession number :
108975323
Full Text :
https://doi.org/10.1586/1744666X.2015.1062366