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Activation of Thymic Regeneration in Mice and Humans following Androgen Blockade
Author(s) -
Jayne S. Sutherland,
Gabrielle L. Goldberg,
Maree V. Hammett,
Adam P. Uldrich,
Stuart P. Berzins,
Tracy Heng,
Bruce R. Blazar,
Jeremy Millar,
Mark Malin,
Ann P. Chidgey,
Richard L. Boyd
Publication year - 2005
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.175.4.2741
Subject(s) - regeneration (biology) , atrophy , androgen , biology , blockade , naive t cell , t cell , transplantation , bone marrow , endocrinology , medicine , immunology , cancer research , immune system , t cell receptor , receptor , microbiology and biotechnology , hormone
The thymus undergoes age-related atrophy, coincident with increased circulating sex steroids from puberty. The impact of thymic atrophy is most profound in clinical conditions that cause a severe loss in peripheral T cells with the ability to regenerate adequate numbers of naive CD4+ T cells indirectly correlating with patient age. The present study demonstrates that androgen ablation results in the complete regeneration of the aged male mouse thymus, restoration of peripheral T cell phenotype and function and enhanced thymus regeneration following bone marrow transplantation. Importantly, this technique is also applicable to humans, with analysis of elderly males undergoing sex steroid ablation therapy for prostatic carcinoma, demonstrating an increase in circulating T cell numbers, particularly naive (TREC+) T cells. Collectively these studies represent a fundamentally new approach to treating immunodeficiency states in humans.

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