A physiological role for inducible FOXP3(+) Treg cells. Lessons from women with reproductive failure

Copyright 2010. Published by Elsevier Inc.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 136(2010), 3 vom: 15. Sept., Seite 432-41
1. Verfasser: Arruvito, Lourdes (VerfasserIn)
Weitere Verfasser: Sotelo, Ana I, Billordo, Ariel, Fainboim, Leonardo
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2010
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Research Support, Non-U.S. Gov't FOXP3 protein, human Forkhead Transcription Factors IL2 protein, human IL6 protein, human Interleukin-2 Interleukin-6 Isoantigens STAT5 Transcription Factor Transforming Growth Factor beta
Beschreibung
Zusammenfassung:Copyright 2010. Published by Elsevier Inc.
We have previously shown a decreased frequency and function of Tregs in women suffering from recurrent spontaneous abortions (RSA). In the current study, we first investigated the expression of FOXP3 after T-cell activation. We observed that expression of FOXP3 in activated PBMCs was already present above baseline before any cell division, indicating that it was induced in cells that were previously negative for this transcription factor. Because RSA women showed a more limited expansion of FOXP3-positive cells, we next assessed the role of IL-2 signaling through STAT5, which is known to be required for generation of inducible Tregs (iTregs). We demonstrated not only that TGF-beta and IL-2 were diminished but also that the IL-2-STAT-5 signaling axis was down regulated in RSA women. Finally, in addition to a limited FOXP3(+) cells expansion in vitro, iTregs from RSA women showed a strikingly lower suppressor activity
Beschreibung:Date Completed 30.08.2010
Date Revised 20.11.2014
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2010.05.002