Complement-induced regulatory T cells suppress T-cell responses but allow for dendritic-cell maturation

W Barchet, JD Price, M Cella, M Colonna… - Blood, 2006 - ashpublications.org
W Barchet, JD Price, M Cella, M Colonna, SK MacMillan, JP Cobb, PA Thompson
Blood, 2006ashpublications.org
Concurrent activation of the T-cell receptor (TCR) and complement regulator CD46 on
human CD4+ T lymphocytes induces Tr1-like regulatory T cells that suppress through IL-10
secretion bystander T-cell proliferation. Here we show that, despite their IL-10 production,
CD46-induced T-regulatory T cells (Tregs) do not suppress the activation/maturation of
dendritic cells (DCs). DC maturation by complement/CD46-induced Tregs is mediated
through simultaneous secretion of GM-CSF and soluble CD40L, factors favoring DC …
Concurrent activation of the T-cell receptor (TCR) and complement regulator CD46 on human CD4+ T lymphocytes induces Tr1-like regulatory T cells that suppress through IL-10 secretion bystander T-cell proliferation. Here we show that, despite their IL-10 production, CD46-induced T-regulatory T cells (Tregs) do not suppress the activation/maturation of dendritic cells (DCs). DC maturation by complement/CD46-induced Tregs is mediated through simultaneous secretion of GM-CSF and soluble CD40L, factors favoring DC differentiation and reversing inhibitory effects of IL-10. Thus, CD46-induced Tregs produce a distinct cytokine profile that inhibits T-cell responses but leaves DC activation unimpaired. Such “DC-sparing” Tregs could be desirable at host/environment interfaces such as the gastrointestinal tract where their specific cytokine profile provides a mechanism that ensures unresponsiveness to commensal bacteria while maintaining reactivity to invading pathogens.
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