CD4+CD25+Foxp3+IFN-γ+ human induced T regulatory cells are induced by interferon-γ and suppress alloresponses nonspecifically

Interferon-γ (IFN-γ)-producing CD3+CD4+CD25+Foxp3+ peripheral blood lymphocytes (PBL) are more frequently detectable in patients with good than in patients with impaired long-term kidney graft function, suggesting an immunoregulatory role of this induced T regulatory (iTreg) subtype. Herein, the in...

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Hauptverfasser: Daniel, Volker (VerfasserIn) , Sadeghi, Mahmoud (VerfasserIn) , Wang, Haihao (VerfasserIn) , Opelz, Gerhard (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2011
In: Human immunology
Year: 2011, Jahrgang: 72, Heft: 9, Pages: 699-707
ISSN:1879-1166
DOI:10.1016/j.humimm.2011.05.020
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.humimm.2011.05.020
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S0198885911001273
Volltext
Verfasserangaben:Volker Daniel, Mahmoud Sadeghi, Haihao Wang, Gerhard Opelz
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Zusammenfassung:Interferon-γ (IFN-γ)-producing CD3+CD4+CD25+Foxp3+ peripheral blood lymphocytes (PBL) are more frequently detectable in patients with good than in patients with impaired long-term kidney graft function, suggesting an immunoregulatory role of this induced T regulatory (iTreg) subtype. Herein, the in vitro function of separated CD3+CD4+CD25+Foxp3+IFN-γ+ PBL that were induced by phorbol 12-myristate 13-acetate (PMA)/ionomycin or alloantigenic stimulation was investigated using cell coculture techniques and flow cytometry. CD4+CD25+Foxp3+ PBL with intracellular IFN-γ production increased to 26% in cell cultures stimulated with PMA/ionomycin for 6 hours. Recombinant IFN-γ augmented and anti-IFN-γ monoclonal antibody blocked induction of CD4+CD25+Foxp3+IFN-γ+ PBL, suggesting their IFN-γ-dependent induction. In addition, CD4+CD25+Foxp3+IFN-γ+ PBL produced immunosuppressive interleukin (IL)-10, transforming growth factor-β, and IL-4 intracellularly and expressed both IFN-γ and IFN-γ receptors (CD119) on the cell surface, allowing separation of CD4+CD25+IFN-γ+ PBL with 98% purity. Addition of enriched CD4+CD25+IFN-γ+ PBL to autologous PMA/ionomycin stimulated PBL decreased blast formation (p < 0.05), indicating suppression of cell proliferation by CD4+CD25+IFN-γ+ PBL. CD4+CD25+IFN-γ+ PBL separated from primary mixed leukocyte cultures (MLC) and added to autologous or third-party secondary MLC suppressed allogeneic T-cell activation nonspecifically (p < 0.05). We conclude that CD4+CD25+Foxp3+IFN-γ+ PBL are induced by IFN-γ, making them sensors for IFN-γ and initial immune responses. Circulating CD4+CD25+Foxp3+IFN-γ+ PBL could suppress allogeneic T-cell responses in patients and may be involved in inhibition of the posttransplant alloresponse.
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Beschreibung:Online Resource
ISSN:1879-1166
DOI:10.1016/j.humimm.2011.05.020