Cutting edge: trans-signaling via the soluble IL-6R abrogates the induction of FoxP3 in naive CD4+CD25 T cells.

Abstract

Chronic inflammatory diseases may develop when regulatory T cells (Tregs) fail to control the balance between tolerance and immunity. Alternatively, activated immune cells might prevent the induction or activation of Tregs in such diseases. In this study, we demonstrate that trans-signaling into T cells via the soluble IL-6 receptor completely abrogates the de novo induction of adaptive Tregs. Mechanistically, IL-6 trans-signaling augmented the expression of the TGF-beta signaling inhibitor SMAD7. Consequently, SMAD7 overexpression in T cells using newly created transgenic mice rendered CD4(+)CD25(-) T cells resistant to the induction of FoxP3. Finally, IL-6 trans-signaling inhibited Treg-mediated suppression in a murine model of colitis. In summary, IL-6 trans-signaling into T cells emerges as a key pathway for blockade of the development of adaptive Tregs and thus may play a pivotal role in shifting the balance between effector and regulatory T cell numbers in chronic inflammatory and autoimmune diseases.

• Authors: Sabine Dominitzki, Massimo C Fantini, Clemens Neufert, Alexei Nikolaev, Peter R Galle, Jürgen Scheller, Giovanni Monteleone, Stefan Rose-John, Markus F Neurath, Christoph Becker
• Journal: Journal of immunology (Baltimore, Md. : 1950) (J Immunol) Vol. 179 Issue 4 Pg. 2041-5 (Aug 15 2007) ISSN: 0022-1767 [Print] United States
• PMID: 17675459 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Forkhead Transcription Factors
• Foxp3 protein, mouse
• IL6 protein, human
• Interleukin-6
• Receptors, Interleukin-6
• Smad7 Protein
• Smad7 protein, mouse
• Transforming Growth Factor beta

Topics

• Animals
• Autoimmune Diseases (genetics, immunology, pathology)
• Chronic Disease
• Colitis (genetics, immunology, metabolism, pathology)
• Disease Models, Animal
• Forkhead Transcription Factors (biosynthesis, genetics, immunology)
• Gene Expression Regulation (immunology)
• Humans
• Inflammation (genetics, immunology, metabolism, pathology)
• Interleukin-6 (immunology, pharmacology)
• Mice
• Mice, Inbred BALB C
• Mice, SCID
• Mice, Transgenic
• Receptors, Interleukin-6 (genetics, immunology, metabolism)
• Signal Transduction (genetics, immunology)
• Smad7 Protein (genetics, immunology, metabolism)
• T-Lymphocytes, Regulatory (immunology, metabolism, pathology)
• Transforming Growth Factor beta (genetics, immunology, metabolism)