Reconstitution of normal megakaryocytopoiesis and immunologic functions in Wiskott-Aldrich syndrome by marrow transplantation following myeloablation and immunosuppression with busulfan and cyclophosphamide

Three patients with Wiskott-Aldrich syndrome received transplants of marrow from their HLA-A, B, C, D identical siblings after myeloablation with busulfan, 2 mg/kg/day x 4 days, followed by immunosuppression with cyclophosphamide, 50 mg/kg/day x 4. Sustained engraftment of lymphoid and hematopoietic elements was documented in each case. Platelet counts in excess of 100,000/cu mm were restored 20--50 days posttransplant and remain in the normal range 6--12 mo later. Platelets exhibit normal size and in vitro aggregation. The patients produce isoagglutinins and antibodies to other polysaccharides. The use of busulfan in moderate dosages as a myeloablative agent, coupled with cyclophosphamide, may offer an improved alternative to the use of lethal total body irradiation as a preparative regimen for complete correction of Wiskott- Aldrich syndrome by marrow transplantation.

[1]  P. Newburger,et al.  Correction of infantile agranulocytosis (Kostmann's syndrome) by allogeneic bone marrow transplantation. , 1980, The American journal of medicine.

[2]  G. Santos,et al.  BONE MARROW TRANSPLANTATION IN THE BUSULFAN‐TREATED RAT: III. RELATIONSHIP BETWEEN MYELOSUPPRESSION AND IMMUNOSUPPRESSION FOR CONDITIONING BONE MARROW RECIPIENTS , 1977, Transplantation.

[3]  Santos Gw Immunosuppression for clinical marrow transplantation. , 1974 .

[4]  R. Storb,et al.  METHOTREXATE REGIMENS FOR CONTROL OF GRAFT-VERSUS-HOST DISEASE IN DOGS WITH ALLOGENEIC MARROW GRAFTS , 1970, Transplantation.

[5]  T. Hovig,et al.  Wiskott—Aldrich Syndrome: Qualitative Platelet Defects and Short Platelet Survival , 1969, British journal of haematology.

[6]  R. Albertini,et al.  Bone-marrow transplantation in a patient with the Wiskott-Aldrich syndrome. , 1968, Lancet.

[7]  T. Waldmann,et al.  The Wiskott-Aldrich syndrome. A disorder with a possible defect in antigen processing or recognition. , 1968, Lancet.

[8]  M. Cooper,et al.  Wiskott-Aldrich syndrome: An immunologic deficiency disease involving the afferent limb of immunity , 1968 .

[9]  J. Heremans,et al.  Immunochemical quantitation of antigens by single radial immunodiffusion. , 1965, Immunochemistry.

[10]  G. Born,et al.  The aggregation of blood platelets , 1963, The Journal of physiology.

[11]  Aldrich Ra,et al.  Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. , 1954 .

[12]  S. J. Baum,et al.  Bone Marrow Transplantation for Aplastic Anemia: Conditioning with Cyclophosphamide plus Low-Dose Total-Body Irradiation , 1979 .