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Circulating Naturally Occurring Antibodies to P2RY2 Are Decreased in Alzheimer's Disease.

Authors :
Jian, Jie-Ming
Fan, Dong-Yu
Cheng, Yuan
Shen, Ying-Ying
Chen, Dong-Wan
Li, Hui-Yun
Chen, Yang
Zhang, Yuan
Zeng, Gui-Hua
Tan, Cheng-Rong
Liu, Yu-Hui
Wang, Yan-Jiang
Source :
Journal of Alzheimer's Disease. 2022, Vol. 87 Issue 2, p711-719. 9p.
Publication Year :
2022

Abstract

<bold>Background: </bold>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 unknown.<bold>Objective: </bold>To explore the alteration of NAbs-P2RY2 in AD patients and its associations with biomarkers and cognition of AD patients.<bold>Methods: </bold>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.<bold>Results: </bold>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. While plasma NAbs-P2RY2-3 levels were negatively associated with brain amyloid burden in AD patients.<bold>Conclusion: </bold>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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13872877
Volume :
87
Issue :
2
Database :
Academic Search Index
Journal :
Journal of Alzheimer's Disease
Publication Type :
Academic Journal
Accession number :
157146109
Full Text :
https://doi.org/10.3233/JAD-215611