Abnormal immune function of B lymphocyte in peripheral blood of Parkinson's disease

淋巴细胞 B细胞 免疫学 调节性B细胞 B细胞激活因子 免疫系统 细胞因子 外周血淋巴细胞 流式细胞术 免疫分型 内科学 医学 生物 白细胞介素10 抗体
作者
Zhuo Zhang,Xin Xie,Ying Cai,Peipei Liu,Shoufeng Liu,Rongjie Chen,Jin Wang,Yue Wang,Yanan Zhao,Zhizhong Zhu,Xinyuan Zhang,Jialing Wu
出处
期刊:Parkinsonism & Related Disorders [Elsevier BV]
卷期号:116: 105890-105890 被引量:14
标识
DOI:10.1016/j.parkreldis.2023.105890
摘要

Parkinson's disease (PD) is associated with peripheral inflammation and abnormal peripheral blood lymphocyte immune responses. Peripheral blood B-lymphocyte subset distributions and whether they are associated with PD are unclear.Sixty-one PD patients and sixty-one one-to-one paired healthy controls (HCs) were enrolled. We used flow cytometry to perform immunophenotyping of peripheral B-lymphocyte, in vitro stimulation and measured serum cytokine. The relationship between variables and PD were assessed.The percentage of naive B cells in blood of PD patients was decreased, whereas the percentages of regulatory B cells (Bregs), plasma blast cells (PBCs), and double-negative (DN) B cells were increased. The absolute counts of B-lymphocyte and naive B cells in blood of PD patients were decreased. Regression analysis revealed that alterations in the absolute counts of B-lymphocyte and the percentage of Bregs and DN B cells were associated with PD. After stimulation, the percentages of Bregs, PBCs, and switched memory (SwM) B cells increased in PD patients. Additionally, increases in GM-CSF-producing B-cell, IFN-γ-producing B-cell, and TNF-α-producing B-cell percentages were noted in PD. Serum levels of a proliferation-inducing ligand (APRIL), B-cell activating factor (BAFF) and soluble CD40 ligand (sCD40L) were elevated in PD and correlated negatively with the UPDRS III score.Abnormal B-lymphocyte immune responses in peripheral blood may contribute to PD development. Alterations in the absolute counts of B-lymphocyte and the percentage of Bregs and DN B cells are associated with PD. Furthermore, APRIL, BAFF, and sCD40L could be potential targets for intervention in PD.
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