Current and emerging treatment options for Wiskott-Aldrich syndrome
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作者:
Worth, Austen J. J.
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Great Ormond St Hosp Natl Hlth Serv Trust, Dept Clin Immunol & Bone Marrow Transplantat, London WC1N 1JH, EnglandGreat Ormond St Hosp Natl Hlth Serv Trust, Dept Clin Immunol & Bone Marrow Transplantat, London WC1N 1JH, England
Worth, Austen J. J.
[1
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Thrasher, Adrian J.
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UCL Inst Child Hlth, Dept Mol & Cellular Immunol, London WC1N 1EN, EnglandGreat Ormond St Hosp Natl Hlth Serv Trust, Dept Clin Immunol & Bone Marrow Transplantat, London WC1N 1JH, England
Thrasher, Adrian J.
[2
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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
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.
机构:
Univ Calif Irvine, Dept Pediat, Irvine, CA 92717 USAUniv Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
Cavannaugh, Corey
Ochs, Hans D.
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Univ Washington, Dept Pediat, Seattle, WA 98195 USA
Seattle Childrens Res Inst Seattle, Seattle, WA USAUniv Calif Irvine, Dept Pediat, Irvine, CA 92717 USA
Ochs, Hans D.
Buchbinder, David
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Childrens Hosp Orange Cty, Div Hematol, 1201 La Veta Ave, Orange, CA 92868 USAUniv Calif Irvine, Dept Pediat, Irvine, CA 92717 USA