TITLE

Regulatory T cells are key cerebroprotective immunomodulators in acute experimental stroke

AUTHOR(S)
Liesz, Arthur; Suri-Payer, Elisabeth; Veltkamp, Claudia; Doerr, Henrike; Sommer, Clemens; Rivest, Serge; Giese, Thomas; Veltkamp, Roland
PUB. DATE
February 2009
SOURCE
Nature Medicine;Feb2009, Vol. 15 Issue 2, p192
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Systemic and local inflammatory processes have a key, mainly detrimental role in the pathophysiology of ischemic stroke. Currently, little is known about endogenous counterregulatory immune mechanisms. We examined the role of the key immunomodulators CD4+CD25+ forkhead box P3 (Foxp3)+ regulatory T lymphocytes (Treg cells), after experimental brain ischemia. Depletion of Treg cells profoundly increased delayed brain damage and deteriorated functional outcome. Absence of Treg cells augmented postischemic activation of resident and invading inflammatory cells including microglia and T cells, the main sources of deleterious cerebral tumor necrosis factor-α (TNF-α) and interferon-γ (IFN-γ), respectively. Early antagonization of TNF-α and delayed neutralization of IFN-γ prevented infarct growth in Treg cell–depleted mice. Intracerebral interleukin-10 (IL-10) substitution abrogated the cytokine overexpression after Treg cell depletion and prevented secondary infarct growth, whereas transfer of IL-10–deficient Treg cells in an adoptive transfer model was ineffective. In conclusion, Treg cells are major cerebroprotective modulators of postischemic inflammatory brain damage targeting multiple inflammatory pathways. IL-10 signaling is essential for their immunomodulatory effect.
ACCESSION #
36386722

 

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