PINK1 is a target of T cell responses in Parkinson's disease
Gregory P. WilliamsiD, Antoine FreuchetiD, Tanner Michaelis, April FrazieriD, Ngan K. TraniD, João Rodrigues Lima-JúnioriD, Elizabeth Jane PhillipsiD, Simon Alexander MallaliD, Irene LitvaniD, Jennifer G. GoldmaniD, Roy N. AlcalayiD, John SidneyiD, David SulzeriD, Alessandro SetteiD, Cecilia S. Lindestam ArlehamniD
Abstract
Parkinsons disease (PD) is associated with autoimmune T cells that recognize the protein alpha-synuclein in a subset of individuals. Multiple neuroantigens are targets of autoinflammatory T cells in classical central nervous system autoimmune diseases such as multiple sclerosis (MS). Here, we explored whether additional autoantigenic targets of T cells in PD. We generated 15-mer peptide pools spanning several PD-related proteins implicated in PD pathology, including GBA, SOD1, PINK1, parkin, OGDH, and LRRK2. Cytokine production (IFN{gamma}, IL-5, IL-10) against these proteins was measured using a fluorospot assay and PBMCs from patients with PD and age-matched healthy controls. This approach identified unique epitopes and their HLA restriction from the mitochondrial-associated protein PINK1, a regulator of mitochondrial stability, as an autoantigen targeted by T cells. The T cell reactivity was predominantly found in male patients with PD, which may contribute to the heterogeneity of PD. Identifying and characterizing PINK1 and other autoinflammatory targets may lead to antigen-specific diagnostics, progression markers, and/or novel therapeutic strategies for PD.
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