Cutting edge: self-peptides drive the peripheral expansion of CD4+ CD25+ regulatory T cells

C Cozzo, J Larkin, AJ Caton - The Journal of Immunology, 2003 - journals.aai.org
C Cozzo, J Larkin, AJ Caton
The Journal of Immunology, 2003journals.aai.org
Abstract CD4+ CD25+ regulatory T cell selection is initiated by high-specificity interactions
with self-peptides in the thymus, although how these cells respond to cytokine-derived
signals and to re-exposure to self-peptide: MHC complexes in the periphery is not well
understood. We have used a transgenic mouse system, in which the peptide that induces
thymic selection of a clonal population of CD4+ CD25+ regulatory T cells is known, to show
that CD4+ CD25+ T cells proliferate in response to their selecting self-peptide in vivo …
Abstract
CD4+ CD25+ regulatory T cell selection is initiated by high-specificity interactions with self-peptides in the thymus, although how these cells respond to cytokine-derived signals and to re-exposure to self-peptide: MHC complexes in the periphery is not well understood. We have used a transgenic mouse system, in which the peptide that induces thymic selection of a clonal population of CD4+ CD25+ regulatory T cells is known, to show that CD4+ CD25+ T cells proliferate in response to their selecting self-peptide in vivo. Moreover, they do not proliferate in response to lymphopenia in the absence of the selecting self-peptide, reflecting a low level of expression of the high affinity receptor for IL-7 (CD127) relative to conventional CD4+ T cells. That their selecting self-peptide is both required for and promotes the peripheral expansion of CD4+ CD25+ regulatory T cells may direct their accumulation in sites where the self-peptide is expressed.
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