Successful allogeneic peripheral blood stem cell transplantation in Wiskott-Aldrich Syndrome Patients: first report in Thailand

Wiskott-Aldrich syndrome (WAS), an X-linked recessive disorder, is characterized by primary progressive T cell immunodeficiency, impaired antipolysaccharide antibody production, eczema, and thrombocytopenia. Stem cell transplantation is the only curative therapy. To evaluate the use of allogeneic pe...

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Bibliographic Details
Published in:	Asian Pacific journal of allergy and immunology Vol. 19; no. 3; p. 191
Main Authors:	Hongeng, S, Benjaponpitak, S, Tardtong, P, Varavithya, W, Chuansumrit, A, Chunharas, A, Chaisiripoomkere, W, Hathira, P
Format:	Journal Article
Language:	English
Published:	Thailand 01-09-2001
Subjects:	Adolescent Child Child, Preschool Graft Survival Graft vs Host Disease - prevention & control Hematopoietic Stem Cell Transplantation HLA Antigens Humans Male Thailand Transplantation Conditioning Transplantation, Homologous Wiskott-Aldrich Syndrome - genetics Wiskott-Aldrich Syndrome - immunology Wiskott-Aldrich Syndrome - therapy Thailand
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Summary:	Wiskott-Aldrich syndrome (WAS), an X-linked recessive disorder, is characterized by primary progressive T cell immunodeficiency, impaired antipolysaccharide antibody production, eczema, and thrombocytopenia. Stem cell transplantation is the only curative therapy. To evaluate the use of allogeneic peripheral stem cell transplantation (PBSCT) in this group of patients, we performed allogeneic PBSCT in two WAS patients (3 and 12 years old). The conditioning regimen consisted of busulfan 4 mg/kg/day for 4 days, and cyclophosphamide 50 mg/kg/day for 4 days. Graft-versus-host disease prophylaxis was consistent with cyclosporin A and methotrexate. Peripheral blood stem cells were collected from their brother donors (6 and 16 years old) by continuous flow leukapheresis after mobilization with granulocyte-colony-stimulating factor at a dose of 7.5 microg/kg/day for 5 days. Both recipients achieved neutrophils engraftment on days 11 and 12. The first patient achieved platelets engraftment on day 30. The second patient did not have platelet count below 20.0 x 10(9)/l during PBSCT procedure. Both did not develop acute or chronic graft-versus-host disease. At present, they are healthy after PBSCT. The follow up time after transplantation is 1,170 days and 269 days, respectively. Allogeneic PBSCT is economically feasible for WAS. The cost of PBSCT in Thailand is 20 to 30% less than bone marrow and cord blood stem cell transplantation. The cost of the transplant procedure for each patient in Thailand is US $ 12,000. This study is the first report of a successful stem cell transplantation in WAS patients in Thailand.
ISSN:	0125-877X