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Hematopoietic stem cell transplantation from matched unrelated donors in chronic granulomatous disease.
Schuetz, C; Hoenig, M; Gatz, S; Speth, F; Benninghoff, U; Schulz, A; Debatin, K M; Friedrich, W.
Affiliation
  • Schuetz C; Department of Paediatrics, University Hospital Ulm, Paediatrics Eythstrasse 24, 89075, Ulm, Germany. catharinaschuetz@gmx.de
Immunol Res ; 44(1-3): 35-41, 2009.
Article in En | MEDLINE | ID: mdl-18846320
ABSTRACT
We report on 12 patients with chronic granulomatous disease transplanted with hematopoietic stem cells from matched unrelated (n = 9) or matched sibling donors (n = 3). The most common infectious complication was pulmonary aspergillosis, which nine patients had previously developed. Only 5 of 12 individuals had normal lung function prior to transplantation. At a mean follow-up of 53 months 9 of the 12 patients are alive including 7 of 9 following matched unrelated donor (MUD) transplantation. One patient died from ARDS, another from systemic BK virus infection, the third from complications of chronic graft-versus-host disease. Seven of nine surviving patients have normal lung function now. HSCT from a MUD is an option worth considering when no matched family donor is available. Restricted lung function prior to HSCT does not appear to be a limiting factor for such treatment.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Granulomatous Disease, Chronic Type of study: Etiology_studies / Observational_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Humans / Male Language: En Journal: Immunol Res Year: 2009 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hematopoietic Stem Cell Transplantation / Granulomatous Disease, Chronic Type of study: Etiology_studies / Observational_studies / Prognostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Humans / Male Language: En Journal: Immunol Res Year: 2009 Document type: Article