4.8 Article

Regulatory T cell differentiation of thymocytes does not require a dedicated antigen-presenting cell but is under T cell-intrinsic developmental control

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.0901877106

Keywords

thymic antigen presenting cell; thymus; tolerance

Funding

  1. Deutsche Forschungsgemeinschaft [SFB 571]
  2. Austrian National Science Fund [F023]
  3. Boehringer Ingelheim

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The majority of regulatory T cells (T-regs) are believed to be of thymic origin. It has been hypothesized that this may result from unique intrathymic environmental cues, possibly requiring a dedicated antigen-presenting cell (APC). However, T cell-intrinsic developmental regulation of the susceptibility to T-reg differentiation remains a mutually non-exclusive scenario. We found that upon exposure of monoclonal T cells of sequential developmental stages to a thymic microenvironment expressing cognate antigen, the efficiency of T-reg induction inversely correlated with progressive maturation. This inclination of immature thymocytes toward T-reg differentiation was even seen in an APC-free in vitro system, providing only TCR stimulation and IL-2. In support of quantitative but not qualitative features of external cues being critical, thymic epithelial cells as well as different thymic dendritic cell (DC)-subtypes efficiently induced T-reg development of immature thymocytes, albeit at strikingly different optimal doses of cognate antigen. We propose that the intrinsically high predisposition of immature thymocytes to T-reg development may contribute to the predominantly thymic origin of the T-reg repertoire. The underlying instructive stimulus, however, does not require unique features of a dedicated APC and can be delivered by hematopoietic as well as epithelial thymic stromal cells.

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