Novel primary thymic defect with T lymphocytes expressing gamma delta T cell receptor

Research output: Contribution to journalJournal articleResearchpeer-review

  • Geisler, Carsten
  • G Pallesen
  • P Platz
  • N Odum
  • E Dickmeiss
  • L P Ryder
  • A Svejgaard
  • T Plesner
  • J K Larsen
  • C Koch
Flow cytometric analysis of the peripheral blood mononuclear cells in a six year old girl with a primary cellular immune deficiency showed a normal fraction of CD3 positive T cells. Most (70%) of the CD3 positive cells, however, expressed the gamma delta and not the alpha beta T cell receptor. Immunoprecipitation and sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) showed that most of the gamma delta T cell receptors existed as disulphide-linked heterodimers. Proliferative responses to mitogens were severely reduced, but specific antibody responses after vaccination could be detected. A thymic biopsy specimen showed severe abnormalities of both the thymic lymphoid and epithelial component with abortive medullary differentiation and almost an entire lack of Hassall's corpuscles. This patient represents a case of primary immune deficiency syndrome not previously described. Thymic deficiency associated with a high proportion of T cells expressing the gamma delta T cell receptor has been described in nude mice, and it is suggested that the immune deficiency of this patient may represent a human analogue.
Original languageEnglish
JournalJournal of Clinical Pathology
Volume42
Issue number7
Pages (from-to)705-11
Number of pages6
ISSN0021-9746
Publication statusPublished - 1989

Bibliographical note

Keywords: Antigens, CD3; Antigens, Differentiation, T-Lymphocyte; Child; Female; Flow Cytometry; Gene Rearrangement, T-Lymphocyte; Humans; Immunologic Deficiency Syndromes; Membrane Glycoproteins; Receptors, Antigen, T-Cell; T-Lymphocytes; Thymus Gland

ID: 8546484