Impaired Negative Selection of T Cells in Hodgkin's Disease Antigen CD30–Deficient Mice

CD30 is found on Reed–Sternberg cells of Hodgkin's disease and on a variety of non-Hodgkin's lymphoma cells and is up-regulated on cells after Epstein–Barr virus, human T cell leukemia virus, and HIV infections. We report here that the thymus in CD30-deficient mice contains elevated number...

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Veröffentlicht in:Cell 1996-02, Vol.84 (4), p.551-562
Hauptverfasser: Amakawa, Ryuichi, Hakem, Anne, Kundig, Thomas M, Matsuyama, Toshifumi, Simard, John J.L, Timms, Emma, Wakeham, Andrew, Mittruecker, Hans-Willi, Griesser, Henrik, Takimoto, Hiroaki, Schmits, Rudolf, Shahinian, Arda, Ohashi, Pamela S, Penninger, Josef M, Mak, Tak W
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Sprache:eng
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Zusammenfassung:CD30 is found on Reed–Sternberg cells of Hodgkin's disease and on a variety of non-Hodgkin's lymphoma cells and is up-regulated on cells after Epstein–Barr virus, human T cell leukemia virus, and HIV infections. We report here that the thymus in CD30-deficient mice contains elevated numbers of thymocytes. Activation-induced death of thymocytes after CD3 cross-linking is impaired both in vitro and in vivo. Breeding the CD30 mutation separately into αβTCR- or γδTCR-transgenic mice revealed a gross defect in negative but not positive selection. Thus, like TNF-receptors and Fas/Apo-1, the CD30 receptor is involved in cell death signaling. It is also an important coreceptor that participates in thymic deletion.
ISSN:0092-8674
1097-4172
DOI:10.1016/S0092-8674(00)81031-4