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Mouse Naïve CD4+ T Cell Isolation and In vitro Differentiation into T Cell Subsets
Published on: April 16, 2015
CD4+ FoxP3+ T regulatory cell subsets in myasthenia gravis patients
Siegfried Kohler1, Thomas Oskar Philipp Keil2, Sarah Hoffmann2
1Department of Experimental Neurology, Charité, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany; Department of Neurology, Charité, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany; NeuroCure Clinical Research Center, Charité, Campus Mitte, Charitéplatz 1, 10117 Berlin, Germany.
Abstract:
Although myasthenia gravis (MG) is a classic autoantibody-mediated disease, T cells are centrally involved in its pathogenesis. In recent years a number of studies have analyzed the role of CD4+ FoxP3+ regulatory T cells (Treg) in the disease with contradictory results. Here, the generation of Treg was significantly reduced in thymoma as compared to thymic hyperplasia and normal thymus tissue (p=0.0002). In the peripheral blood, Treg subsets classified according to CD49d, HELIOS and CD45RA expression changed after thymectomy and in the long-term course of immunosuppression. Compared to healthy volunteers the frequency of CD45RA+FoxP3low Treg was reduced in MG patients in general (p=0.037) and in particular in patients without immunosuppression (p=0.036). In our study, thymectomy and immunosuppressive treatment were associated with changes in Treg subpopulations. The reduced frequency of CD45RA+FoxP3low Treg we observed in MG patients might play a role in MG pathogenesis.
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