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Tolerance without Clonal Expansion: Self-Antigen-Expressing B Cells Program Self-Reactive T Cells for Future Deletion
Author(s) -
Friederike Frommer,
Tobias Heinen,
F. Thomas Wunderlich,
Nir Yogev,
Thorsten Buch,
Axel Roers,
Estelle Bettelli,
Werner Müller,
Stephen M. Anderton,
Ari Waisman
Publication year - 2008
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.181.8.5748
Subject(s) - microbiology and biotechnology , interleukin 21 , biology , immune system , b 1 cell , antigen presenting cell , antigen , cd40 , il 2 receptor , cytotoxic t cell , naive b cell , immune tolerance , t cell , natural killer t cell , immunology , in vitro , genetics
B cells have been shown in various animal models to induce immunological tolerance leading to reduced immune responses and protection from autoimmunity. We show that interaction of B cells with naive T cells results in T cell triggering accompanied by the expression of negative costimulatory molecules such as PD-1, CTLA-4, B and T lymphocyte attenuator, and CD5. Following interaction with B cells, T cells were not induced to proliferate, in a process that was dependent on their expression of PD-1 and CTLA-4, but not CD5. In contrast, the T cells became sensitive to Ag-induced cell death. Our results demonstrate that B cells participate in the homeostasis of the immune system by ablation of conventional self-reactive T cells.

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