Abstract

Background In Systemic Sclerosis (SSc) the detrimental role of the immune system is a topic of great interest. In recent genetic association studies most genes identified to date are immunity related genes. A contribution of T-cells as important cytokine producing cells is shown and the skewing of this population can be an important player in the maintenance and progression of inflammation and fibrosis.

Highlights

  • In Systemic Sclerosis (SSc) the detrimental role of the immune system is a topic of great interest

  • The decreased production of IL-10 and interferon-g in limited SSc patients shows a decrease of Th1 and Treg involvement in this disease subset

  • A prospective study must show if these findings could contribute to the assessing the prognosis and the treatment of SSc patients

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Summary

Background

In Systemic Sclerosis (SSc) the detrimental role of the immune system is a topic of great interest. In recent genetic association studies most genes identified to date are immunity related genes. A contribution of T-cells as important cytokine producing cells is shown and the skewing of this population can be an important player in the maintenance and progression of inflammation and fibrosis. Together with a normal production of IL-13 this could create a proinflmmatory and profibrotic condition in this subset of patients. The decreased production of IL-10 and interferon-g in limited SSc patients shows a decrease of Th1 and Treg involvement in this disease subset. A prospective study must show if these findings could contribute to the assessing the prognosis and the treatment of SSc patients

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