Abstract
CD30 is a member of the TNF receptor superfamily that is commonly used as a marker for Hodgkin and Reed-Sternberg cells in Hodgkin's disease. More recently, it has been proposed that CD30 is preferentially up-regulated on Th2-type human T cells. We analyzed regulation of CD30 expression on both peripheral blood T cells and T cell clones. In short-term culture, CD30 expression could be induced on T cells by Ags that elicit Th2-type responses (Schistosoma haematobium, adult worm Ag, and Toxocaria canis, excretory/secretory Ag) and Th0-type responses (tetanus toxoid), as well as Th1-type responses (tuberculin purified protein derivative). Moreover, simultaneous measurement of membrane phenotype and cytokine production showed that CD30-expressing cells can produce IFN-gamma. Finally, within panels of randomly generated as well as Ag-specific T cell clones, CD30 expression was found on Th0-, Th2-, and Th1-type clones. We conclude that induction of CD30 on activated T cells is not related to differentiation in Th0-, Th1-, or Th2-type cells.
Original language | English |
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Pages (from-to) | 1387-91 |
Number of pages | 5 |
Journal | Journal of Immunology |
Volume | 156 |
Issue number | 4 |
Publication status | Published - 15 Feb 1996 |
Externally published | Yes |
Keywords
- Cell Differentiation
- Humans
- Interferon-gamma/biosynthesis
- Ki-1 Antigen/metabolism
- Lymphocyte Activation
- Th1 Cells/immunology
- Th2 Cells/immunology
- Up-Regulation