Abstract |
Thymus transplantation is a promising investigational therapy for infants born with no thymus. Because of the athymia, these infants lack T cell development and have a severe primary immunodeficiency. Although thymic hypoplasia or aplasia is characteristic of DiGeorge anomaly, in "complete" DiGeorge anomaly, there is no detectable thymus as determined by the absence of naive (CD45RA(+), CD62L(+)) T cells. Transplantation of postnatal allogeneic cultured thymus tissue was performed in sixty subjects with complete DiGeorge anomaly who were under the age of 2 years. Recipient survival was over 70%. Naive T cells developed 3-5 months after transplantation. The graft recipients were able to discontinue antibiotic prophylaxis, and immunoglobulin replacement. Immunosuppression was used in a subset of subjects but was discontinued when naive T cells developed. The adverse events have been acceptable with thyroid disease being the most common. Research continues on mechanisms underlying immune reconstitution after thymus transplantation.
|
Authors | M Louise Markert, Blythe H Devlin, Elizabeth A McCarthy |
Journal | Clinical immunology (Orlando, Fla.)
(Clin Immunol)
Vol. 135
Issue 2
Pg. 236-46
(May 2010)
ISSN: 1521-7035 [Electronic] United States |
PMID | 20236866
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
|
Copyright | Copyright 2010 Elsevier Inc. All rights reserved. |
Topics |
- Cell Count
- DiGeorge Syndrome
(immunology, surgery)
- Humans
- Infant
- T-Lymphocytes
(immunology, transplantation)
- Thymus Gland
(immunology, transplantation)
- Transplantation, Homologous
(adverse effects, immunology, methods)
- Treatment Outcome
|