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February 11, 2026Scandinavian Journal of Immunology0 citationsOpen Access

Role of CXCR3 and CXCR6 on Circulating T Cells in Patients With Parkinson's Disease

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PZPeng ZhangZRZhuangzhuang RenSJShuangshuang Jia

Key Points

  • The research aims to clarify the roles of CXCR3 and CXCR6 on T cells and their association with inflammation in Parkinson's disease.
  • Enrolled 36 patients with Parkinson's disease and 26 healthy controls
  • Collected clinical and laboratory test data, including inflammation-related indices
  • Used multicolour flow cytometry to assess T cell markers and receptor expression
  • CD8+ T cells are significantly reduced in Parkinson's disease patients compared to healthy controls (p < 0.001)
  • CXCR3 expression is significantly higher in peripheral blood CD4+ and CD8+ T cells of PD patients (p < 0.001)
  • CXCR6 expression is notably elevated on cytotoxic T lymphocytes of PD patients (p < 0.0001)
  • Significantly increased C-reactive protein levels in PD patients (p < 0.001) but reduced monocytes and lymphocytes (p < 0.01)

Abstract

ABSTRACT Immune dysregulation is involved in Parkinson's disease (PD), but the roles of C‐X‐C motif chemokine receptor 3 (CXCR3)/chemokine receptor 6 (CXCR6) on T cells and their correlation with peripheral inflammation remain unclear. This study investigated their expression on peripheral blood T cells and correlation with inflammation in PD. A total of 36 PD patients and 26 healthy controls were enrolled; their clinical information and laboratory test results (including the systemic immunoinflammatory index SII, neutrophil‐to‐lymphocyte ratio NLR, monocyte‐to‐lymphocyte ratio MLR, platelet‐to‐lymphocyte ratio PLR, monocyte‐to‐high‐density lipoprotein ratio MHR, and erythrocyte distribution width over platelets ratio RPR) were recorded. Meanwhile, a multicolour flow cytometry protocol using six cell surface antibodies (CD3, CD4, CD8, CD45RO, CXCR3, and CXCR6) was applied. The results showed that CD8 + T cells were significantly reduced in the PD group compared with healthy controls ( p 0.05). Compared with healthy controls, PD patients had significantly increased peripheral blood C‐reactive protein (CRP) levels ( p < 0.001) but remarkably decreased monocytes, lymphocytes, and MHR ( p < 0.01). Collectively, the upregulated expression of CXCR3 and CXCR6 predominantly on CD8 + T lymphocytes may contribute to PD pathogenesis, though no significant correlation between the expression of these receptors and peripheral inflammation was observed.

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Cite This Study

Zhang et al. (2026) studied this question.

synapsesocial.com/papers/698c1c73267fb587c655eee5https://doi.org/10.1111/sji.70090
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