| Literature DB >> 9083893 |
C M Davis1, T M McLaughlin, T J Watson, R H Buckley, S E Schiff, L P Hale, B F Haynes, M L Markert.
Abstract
Complete DiGeorge syndrome is an immunodeficiency disease characterized by thymic aplasia and the absence of functioning peripheral T cells. A patient with this syndrome was transplanted with cultured postnatal human thymic tissue. Within 5 weeks of transplantation, flow cytometry, T cell receptor V beta sequence analysis, and cell function studies showed the presence of oligoclonal populations of nonfunctional clonally expanded peripheral T cells that were derived from pretransplantation T cells present in the skin. However, at 3 months posttransplantation, a biopsy of the transplanted thymus showed normal intrathymic T cell maturation of host T cells with normal TCR V beta expression on thymocytes. By 9 months postransplantation, peripheral T cell function was restored and the TCR V beta repertoire became polyclonal, coincident with the appearance of normal T cell function. These data suggest that the transplanted thymus was responsible for the establishment of a new T cell repertoire via thymopoiesis in the chimeric thymic graft.Entities:
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Year: 1997 PMID: 9083893 DOI: 10.1023/a:1027382600143
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317