Article abstract


Nature Immunology 9, 1341 - 1346 (2008)
Published online: 19 October 2008 | doi:10.1038/ni.1659

Transforming growth factor-bold beta 'reprograms' the differentiation of T helper 2 cells and promotes an interleukin 9–producing subset

Marc Veldhoen1, Catherine Uyttenhove2, Jacques van Snick2, Helena Helmby3, Astrid Westendorf4, Jan Buer4, Bruno Martin1, Christoph Wilhelm1 & Brigitta Stockinger1


Since the discovery of T helper type 1 and type 2 effector T cell subsets 20 years ago, inducible regulatory T cells and interleukin 17 (IL-17)-producing T helper cells have been added to the 'portfolio' of helper T cells. It is unclear how many more effector T cell subsets there may be and to what degree their characteristics are fixed or flexible. Here we show that transforming growth factor-beta, a cytokine at the center of the differentiation of IL-17-producing T helper cells and inducible regulatory T cells, 'reprograms' T helper type 2 cells to lose their characteristic profile and switch to IL-9 secretion or, in combination with IL-4, drives the differentiation of 'TH-9' cells directly. Thus, transforming growth factor-beta constitutes a regulatory 'switch' that in combination with other cytokines can 'reprogram' effector T cell differentiation along different pathways.

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  1. Division of Molecular Immunology, Medical Research Council National Institute for Medical Research, London NW7 1AA, UK.
  2. Ludwig Institute for Cancer Research, Brussels Branch, Cellular Genetics Unit and Experimental Medicine Unit, Christian de Duve Institute of Cellular Pathology, Université de Louvain, 1200 Brussels, Belgium.
  3. London School of Hygiene and Tropical Medicine, London WC1E 7HT, UK.
  4. Institute of Medical Microbiology, University of Duisburg-Essen, D-45122 Essen, Germany.

Correspondence to: Brigitta Stockinger1 e-mail: bstocki@nimr.mrc.ac.uk



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