Successful nonsibling bone marrow transplantation in severe combined immunodeficiency

Severe combined immunodeficiency (SCID) was diagnosed in a girl immediately after birth; her older brother had SCID and was successfully reconstituted by bone marrow transplantation from his uncle. She was isolated in a laminar air flow bench and decontaminated. The father differed by one HLA-A anti...

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Veröffentlicht in:Transplantation 1978-12, Vol.26 (6), p.369-372
Hauptverfasser: Ramsøe, K, Skinhøj, P, Andersen, V, Ernst, P, Faber, V, Platz, P, Thomsen, M, Svejgaard, A, Eriksen, K R, Plesner, T, Morling, N, Philip, J, Killmann, S A, Koch, C, Muller-Bérat, N, Henningsen, K, Axelsen, H
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Sprache:eng
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Zusammenfassung:Severe combined immunodeficiency (SCID) was diagnosed in a girl immediately after birth; her older brother had SCID and was successfully reconstituted by bone marrow transplantation from his uncle. She was isolated in a laminar air flow bench and decontaminated. The father differed by one HLA-A antigen but was HLA-Dw2 homozygous like the patient; his lymphocytes showed a slight response to the patient's cells in mixed lymphocyte culture (MLC). At the age of 2 1/2 months and again at 5 months, she was given a bone marrow transplant from the father. During the entire course the patient had no infections, and apart from a transient eosinophilia she had no signs of graft-versus-host reaction. Immunological reconstitution was nearly complete at 9 months of age, when she was recontaminated. One year later plasma immunoglobulin concentrations are in the low normal range (IgG and IgM) or decreased (IgA); tests of cell-mediated immunity are normal. Apart from slight upper respiratory infections, the patient has been healthy. Physical and psychological development have been normal.
ISSN:0041-1337
DOI:10.1097/00007890-197812000-00001