The induction of antigen-specific tolerance in the mature immune system of the intact organism has met with limited success. Therefore, nonspecific immunosuppression has been the treatment of choice to prevent unwanted immunity. Here, it is shown that prolonged subcutaneous infusion of low doses of peptide by means of osmotic pumps transforms mature T cells into CD4+25+ suppressor cells that can persist for long periods of time in the absence of antigen and confer specific immunologic tolerance upon challenge with antigen. The described procedure resembles approaches of tolerance induction used decades ago, induces tolerance in the absence of immunity, and holds the promise to become an effective means of inducing antigen-specific tolerance prospectively, whereas its power to suppress already ongoing immune responses remains to be determined.
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17 May 2004
Article|
May 17 2004
In Vivo Instruction of Suppressor Commitment in Naive T Cells
Irina Apostolou,
Irina Apostolou
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115
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Harald von Boehmer
Harald von Boehmer
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115
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Irina Apostolou
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115
Harald von Boehmer
Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115
Address correspondence to Harald von Boehmer, Dana-Farber Cancer Institute, Harvard Medical School, 44 Binney St., Boston, MA 02115. Phone: (617) 632-6882; Fax: (617) 632-6881; email: [email protected]
Abbreviations used in this paper: BrdU, 5-bromodeoxyuridine; CFSE, 5,6-carboxyfluorescein diacetate-succinimidyl ester; INS-HA, rat insulin promoter; Tx, thymectomized.
Received:
February 09 2004
Accepted:
April 08 2004
Online ISSN: 1540-9538
Print ISSN: 0022-1007
The Rockefeller University Press
2004
J Exp Med (2004) 199 (10): 1401–1408.
Article history
Received:
February 09 2004
Accepted:
April 08 2004
Citation
Irina Apostolou, Harald von Boehmer; In Vivo Instruction of Suppressor Commitment in Naive T Cells . J Exp Med 17 May 2004; 199 (10): 1401–1408. doi: https://doi.org/10.1084/jem.20040249
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