A distinct subset of HLA-DR+-regulatory T cells is involved in the induction of preterm labor during pregnancy and in the induction of organ rejection after transplantation
Regulatory T cells (Tregs) are known to suppress alloimmune responses during pregnancy and post organ transplantation. We demonstrate that a distinct subset of FoxP3+DR+-Tregs among the total CD4+CD127low+/−CD25+-Treg cell pool is critically involved in preterm labor induction and kidney transplant...
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| Hauptverfasser: | , , , , , , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
6 September 2010
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| In: |
Clinical immunology
Year: 2010, Jahrgang: 137, Heft: 2, Pages: 209-220 |
| ISSN: | 1521-7035 |
| DOI: | 10.1016/j.clim.2010.07.008 |
| Online-Zugang: | Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.clim.2010.07.008 Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S1521661610006741 |
| Verfasserangaben: | Anna Kisielewicz, Matthias Schaier, Edgar Schmitt, Friederike Hug, Gertrud M. Haensch, Stefan Meuer, Martin Zeier, Christof Sohn, Andrea Steinborn |
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| 245 | 1 | 2 | |a A distinct subset of HLA-DR+-regulatory T cells is involved in the induction of preterm labor during pregnancy and in the induction of organ rejection after transplantation |c Anna Kisielewicz, Matthias Schaier, Edgar Schmitt, Friederike Hug, Gertrud M. Haensch, Stefan Meuer, Martin Zeier, Christof Sohn, Andrea Steinborn |
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| 520 | |a Regulatory T cells (Tregs) are known to suppress alloimmune responses during pregnancy and post organ transplantation. We demonstrate that a distinct subset of FoxP3+DR+-Tregs among the total CD4+CD127low+/−CD25+-Treg cell pool is critically involved in preterm labor induction and kidney transplant rejection as well. Compared to healthy pregnancies and non-rejecting kidney recipients, we found that the percentage of the FoxP3+DR+-Treg subset was not reduced, but that the level of HLA-DR expression of such Tregs was strongly diminished in preterm laboring women and in patients with acute renal allograft rejection. In addition, both patient collectives showed a significantly reduced suppressive activity of their circulating CD4+CD127low+/−CD25+-Treg cell pool. Our findings propose that the FoxP3+DR+-Treg subset may be decisively responsible for the suppressive activity of the total CD4+CD127low+/−CD25+-Treg cell pool and that the immunologic mechanisms leading to preterm labor necessitating preterm delivery may be similar to those leading to allograft rejection after transplantation. | ||
| 650 | 4 | |a Pregnancy | |
| 650 | 4 | |a Preterm labor | |
| 650 | 4 | |a Regulatory T cells | |
| 650 | 4 | |a Renal transplantation | |
| 650 | 4 | |a Tolerance induction | |
| 650 | 4 | |a Transplant rejection | |
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