Article Dans Une Revue Journal of Immunology Année : 2009

Cutting Edge: CD4-Independent Development of Functional FoxP3+ Regulatory T Cells

Résumé

The CD4 coreceptor is mandatory for the differentiation and function of conventional MHC class II-restricted T cells, but little is known about its contribution in regulatory T cells (Tregs). We thus investigated the Treg compartment in mice lacking CD4. CD3+CD8−FoxP3+ cells were readily detected in the periphery of CD4−/− mice, where their percentages were even increased as compared with wild-type animals. These cells had a classical CD25+CD152+GITR+ Treg phenotype, were enriched in memory-type Tregs, and displayed a diversified TCR repertoire. Functionally, CD4−/− Tregs were equally as suppressive as CD4+/+ Tregs in vitro as well as in vivo. Hence, the CD4 coreceptor is dispensable for the generation and function of FoxP3+ Tregs. Furthermore, CD3+CD8−FoxP3+ Tregs were also found to develop in the absence of both CD4 and MHC-II molecules, demonstrating that the generation of Tregs can occur independently of MHC-II recognition.

Dates et versions

hal-05224640 , version 1 (26-08-2025)

Identifiants

Citer

Céline Blache, Sahil Adriouch, Sébastien Calbo, Laurent Drouot, Sophie Dulauroy, et al.. Cutting Edge: CD4-Independent Development of Functional FoxP3+ Regulatory T Cells. Journal of Immunology, 2009, 183 (7), pp.4182-4186. ⟨10.4049/jimmunol.0901678⟩. ⟨hal-05224640⟩
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