发病机制
抗体
自身抗体
免疫学
医学
疾病
痴呆
淀粉样蛋白(真菌学)
阿尔茨海默病
受体
作者
Jie-Ming Jian,Dong-Yu Fan,Yuan Cheng,Ying-Ying Shen,Dong-Wan Chen,Hui-Yun Li,Yang Chen,Yuan Zhang,Gui-Hua Zeng,Cheng-Rong Tan,Yu-Hui Liu,Yan-Jiang Wang
摘要
Background: The G protein-coupled receptor P2RY2 protein of the purinergic receptor family is involved in the pathogenesis of Alzheimer’s disease (AD). Naturally occurring antibodies against P2RY2 (NAbs-P2RY2) are present in human plasma, with their clinical relevance in AD patients unknown. Objective: To explore the alteration of NAbs-P2RY2 in AD patients and its correlations with biomarkers and cognition of AD. Methods: The levels of naturally occurring antibodies against the four extracellular domains of P2RY2 (NAbs-P2RY2-1, NAbs-P2RY2-2, NAbs-P2RY2-3, and NAbs-P2RY2-4) were measured in the plasma of 55 AD patients, 28 non-AD dementia patients, and 70 cognitively normal participants. The correlations of autoantibody levels with cognitive scale scores, AD plasma biomarkers, and brain amyloid burden were examined. Results: NAbs-P2RY2-1, NAbs-P2RY2-3, and NAbs-P2RY2-4 were reduced in AD patients. Plasma levels of NAbs-P2RY2-2 and NAbs-P2RY2-3 levels were positively associated with cognitive and functional performances. Among these antibodies, plasma NAbs-P2RY2-2 levels were positively associated with plasma amyloid-β 42 levels. Plasma, while plasma NAbs-P2RY2-3 levels were negatively associated with brain amyloid burden in AD patients. Conclusion: These findings indicate an alteration of humoral immunity against P2RY2 in AD patients. Further mechanistical investigations are needed to reveal the role of NAbs-P2RY2 in the pathogenesis of AD.
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