Differential memory enrichment of cytotoxic CD4 T cells in Parkinson’s disease patients reactive to ⍺-synuclein

Parkinson’s disease (PD) is a complex neurodegenerative disease with a largely unknown etiology. Although the loss of dopaminergic neurons in the substantia nigra pars compacta is the pathological hallmark of PD, neuroinflammation also plays a fundamental role in PD pathology. We have previously reported that PD patients have increased frequencies of T cell reactive to peptides from ⍺-synuclein (⍺-syn). However, not all PD participants respond to ⍺-syn. Furthermore, we have previously found that CD4 T cells from PD participants responding to ⍺-syn (PD_R) are transcriptionally distinct from PD participants not responding to ⍺-syn (PD_NR). To gain further insight into the pathology of PD_R participants, we investigated surface protein expression of 11 proteins whose genes had previously been found to be differentially expressed when comparing PD_R and healthy control participants not responding to ⍺-syn (HC_NR). We found that Cadherin EGF LAG seven-pass G-type receptors 2 (CELSR2) was expressed on a significantly higher proportion of CD4 effector memory T cells (Tem) in PD_R compared to HC_NR. Single-cell RNA sequencing analysis of cells expressing or not expressing CELSR2 revealed that PD_R participants have elevated frequencies of activated Tem subsets and an almost complete loss of cytotoxic Tem cells. Flow cytometry analyses confirmed that Granulysin+ CD4 cytotoxic Tem cells are reduced in PD_R. Taken together, these results provide further insight into the perturbation of T cell subsets in PD_R, and highlights the need for further investigation into the role of Granulysin+ CD4 cytotoxic Tem in PD pathology. We set out to perform single cell RNA sequencing to determine the impact of CELSR2 expression of CD4+ effector memory T cells in donors with Parkinsons's disease (PD) resonsive to alpha-synuclein (PD_R) and healthy donor not responsive to alpha-synuclein (HC_NR). 20x10^6 cells per participant were used. Fc receptors were blocked (BD Biosciences) before membrane staining with antibodies and a specific hashtag (TotalSeq B; Biolegend) for 20 min at 4C. Cells were washed and DAPI was added to stain dead cells. Two populations were sorted using a BD FACSAria II (BD Biosciences): DAPI-CD3+CD4+CD8-CD45RA-CCR7-CESLR2+ and DAPI-CD3+CD4+CD8-CD45RA-CCR7-CESLR2-.