Abstract
Naturally occurring CD4+ regulatory T cells can be identified on the basis of expression of CD25 and suppression of T cell responses in vitro after TCR triggering. Here, we demonstrate that a CD134+ subset of CD4+CD25+ T cells in naive rats suppresses antigen-specific T cell responses in vitro without additional TCR stimulation. In contrast, CD4+CD25+CD134- regulatory T cells and total CD4+CD25+ regulatory T cells have suppressive activity only during simultaneous activation of responder and regulatory T cells or after in vitro pre-activation. Furthermore CD4+CD25+CD134+ T cells have a more activated phenotype than CD4+CD25+CD134- T cells, as based on the expression of CD62L, CD45RC, and MHC class II. We propose that the CD134+ regulatory T cells contain an in vivo activated and highly suppressive regulatory T cell subset. CD4+CD25+CD134+ T cells can be found in several compartments of the immune system, including spleen, lymph nodes, and blood. Interestingly though, the relative amounts of these cells within the CD4+ population and their CD134 expression levels are highest in mucosa-draining lymph nodes and lowest in blood. This suggests that the presence of CD4+CD25+CD134+ T cells indicates sites of active immune suppression.
Original language | English |
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Pages (from-to) | 3016-27 |
Number of pages | 12 |
Journal | European Journal of Immunology |
Volume | 34 |
Issue number | 11 |
DOIs | |
Publication status | Published - Nov 2004 |
Keywords
- Animals
- CD4-Positive T-Lymphocytes
- Cell Proliferation
- Epitopes, T-Lymphocyte
- Flow Cytometry
- Gene Expression Regulation
- Immunophenotyping
- Lymph Nodes
- Lymphocyte Activation
- Male
- Rats
- Rats, Inbred Lew
- Receptors, Antigen, T-Cell
- Receptors, Interleukin-2
- Receptors, OX40
- Receptors, Tumor Necrosis Factor
- Spleen
- T-Lymphocyte Subsets