The role of immune dysregulation of innate and adaptive immune cells in the prodromal and clinical stages of Parkinson’s disease

Abstract Background Peripheral blood mononuclear cells (PBMCs) were obtained from patients across different stages of Parkinson’s disease (PD) progression and stimulated ex vivo to develop biomarkers for predicting PD progression. Method PBMCs obtained at one time‐point from patients with moderate stage PD (>5 years after diagnosis) (n = 30), early stage PD (<5 years after diagnosis) (n = 27), prodromal PD (rapid‐eye‐movement sleep behavior disorder patients) (n = 14), and healthy controls (HCs) (n = 9) were isolated from whole blood and cryopreserved. Samples were thawed, then pan‐monocytes and T‐cell populations were isolated from PBMCs and subjected to treatment with vehicle or IFN‐γ. An additional treatment condition with CD3/28 magnetic beads was included for T‐cells. Cultured media was kept for evaluation of cell‐type specific cytokine release, and live cells were analyzed with flow cytometry for markers of immune activation, mitochondrial and lysosomal function, and LRRK2 expression and activity. Result In classical, intermediate, and non‐classical monocytes from HCs, expression of pRab10, LRRK2, and MHC‐II increases after treatment with ex vivo IFN‐γ stimulation. In CD4+ and CD8+ T‐cells from HCs, IFN‐γ and CD3/28 bead treatment caused increased expression of pRab10. CD3/28 magnetic beads, but not IFN‐γ, caused increased expression of CD137 and LRRK2, while also leading to reduced levels of acidified lysosomes. Studies are currently underway to analyze cells from PD and prodromal patients and evaluate cell‐type specific cytokine release in the conditioned media. Conclusion We have applied a validated ex vivo stimulation protocol using PBMCs from PD patients across different stages of disease to measure immune cell activation and cell‐type specific cytokine release. If our hypothesis is correct, we expect that immune cell subsets from PD patients will display a signature of dysregulated immune response to stimulation. Furthermore, we expect that prodromal PD patients will exhibit dysregulated peripheral immune responses compared to controls, including altered mitochondrial and lysosomal function and cytokine release.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.085589
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
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article

The role of immune dysregulation of innate and adaptive immune cells in the prodromal and clinical stages of Parkinson’s disease

Malu Gámez Tansey, Rebecca L. Wallings, Julian R Mark, Hannah A. Staley
Alzheimer s & Dementia
Neuroinflammation and Neurodegeneration Mechanisms
article

The role of immune dysregulation of innate and adaptive immune cells in the prodromal and clinical stages of Parkinson’s disease

Malu Gámez Tansey, Rebecca L. Wallings, Julian R Mark, Hannah A. Staley
article en

Abstract

Abstract Background Peripheral blood mononuclear cells (PBMCs) were obtained from patients across different stages of Parkinson’s disease (PD) progression and stimulated ex vivo to develop biomarkers for predicting PD progression. Method PBMCs obtained at one time‐point from patients with moderate stage PD (>5 years after diagnosis) (n = 30), early stage PD (<5 years after diagnosis) (n = 27), prodromal PD (rapid‐eye‐movement sleep behavior disorder patients) (n = 14), and healthy controls (HCs) (n = 9) were isolated from whole blood and cryopreserved. Samples were thawed, then pan‐monocytes and T‐cell populations were isolated from PBMCs and subjected to treatment with vehicle or IFN‐γ. An additional treatment condition with CD3/28 magnetic beads was included for T‐cells. Cultured media was kept for evaluation of cell‐type specific cytokine release, and live cells were analyzed with flow cytometry for markers of immune activation, mitochondrial and lysosomal function, and LRRK2 expression and activity. Result In classical, intermediate, and non‐classical monocytes from HCs, expression of pRab10, LRRK2, and MHC‐II increases after treatment with ex vivo IFN‐γ stimulation. In CD4+ and CD8+ T‐cells from HCs, IFN‐γ and CD3/28 bead treatment caused increased expression of pRab10. CD3/28 magnetic beads, but not IFN‐γ, caused increased expression of CD137 and LRRK2, while also leading to reduced levels of acidified lysosomes. Studies are currently underway to analyze cells from PD and prodromal patients and evaluate cell‐type specific cytokine release in the conditioned media. Conclusion We have applied a validated ex vivo stimulation protocol using PBMCs from PD patients across different stages of disease to measure immune cell activation and cell‐type specific cytokine release. If our hypothesis is correct, we expect that immune cell subsets from PD patients will display a signature of dysregulated immune response to stimulation. Furthermore, we expect that prodromal PD patients will exhibit dysregulated peripheral immune responses compared to controls, including altered mitochondrial and lysosomal function and cytokine release.

Alzheimer s & DementiaVol. 20(S2)
University of Florida (US), Florida College (US)
Good health and well-being
Openalex Percentile: Top 71%
Neuroinflammation and Neurodegeneration Mechanisms
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