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Peripheral immune cell response to stimulation stratifies Parkinson’s disease progression from prodromal to clinical stages
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AbstractThe motor stage of idiopathic Parkinson’s disease (iPD) can be preceded for years by a prodromal stage characterized by non-motor symptoms like REM sleep behavior disorder (RBD). Here, we show that multiple stages of iPD, including the pre-motor prodromal stage, can be stratified according to the inflammatory and immunometabolic responses to stimulation of peripheral blood mononuclear cellsex vivo. We identified increased stimulation-dependent secretion of TNF, IL-1β, and IL-8 in monocytes from RBD patients and showed diminished proinflammatory cytokine secretion in monocytes and T cells in early and moderate stages of PD. Mechanistically, immune activation revealed deficits in CD8+T-cell mitochondrial health in moderate PD, and relative mitochondrial health in CD8+T cells was positively correlated with stimulation-dependent T-cell cytokine secretion across the PD spectrum. Dysregulated immunometabolism may drive peripheral inflammation and PD progression, andex vivostimulation-based assays have potential to reveal novel biomarkers for patient stratification and progression with immune endophenotypes.
Cold Spring Harbor Laboratory
Title: Peripheral immune cell response to stimulation stratifies Parkinson’s disease progression from prodromal to clinical stages
Description:
AbstractThe motor stage of idiopathic Parkinson’s disease (iPD) can be preceded for years by a prodromal stage characterized by non-motor symptoms like REM sleep behavior disorder (RBD).
Here, we show that multiple stages of iPD, including the pre-motor prodromal stage, can be stratified according to the inflammatory and immunometabolic responses to stimulation of peripheral blood mononuclear cellsex vivo.
We identified increased stimulation-dependent secretion of TNF, IL-1β, and IL-8 in monocytes from RBD patients and showed diminished proinflammatory cytokine secretion in monocytes and T cells in early and moderate stages of PD.
Mechanistically, immune activation revealed deficits in CD8+T-cell mitochondrial health in moderate PD, and relative mitochondrial health in CD8+T cells was positively correlated with stimulation-dependent T-cell cytokine secretion across the PD spectrum.
Dysregulated immunometabolism may drive peripheral inflammation and PD progression, andex vivostimulation-based assays have potential to reveal novel biomarkers for patient stratification and progression with immune endophenotypes.
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