Soluble TREM2 and Inflammatory Proteins in Alzheimer’s Disease Cerebrospinal Fluid

特雷姆2 神经退行性变 脑脊液 阿尔茨海默病 细胞因子 免疫学 小胶质细胞 医学 神经炎症 肿瘤坏死因子α 疾病 内科学 炎症
作者
Boris‐Stephan Rauchmann,Angélique Sadlon,Robert Perneczky
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
卷期号:73 (4): 1615-1626 被引量:35
标识
DOI:10.3233/jad-191120
摘要

The present study explores the associations of soluble TREM2, an important regulator of microglial activity linked to Alzheimer's disease (AD), with other known inflammatory proteins in cerebrospinal fluid (CSF). We studied 303 participants, including 89 controls, 135 mild cognitive impairment, and 79 AD dementia patients. Using established CSF biomarkers, subjects were classified according to the National Institute on Aging-Alzheimer's Association research framework, which groups markers into those of amyloid-β deposition (A), tau pathology (T), and neurodegeneration (N). TNFR1, TNFR2, TGF-β1, TGFβ2, IL-9, TNF-α, ICAM1, and VCAM1 showed significant concentration differences between the ATN groups, with higher concentrations in more advanced disease categories. sTREM2 was positively associated with the pro-inflammatory proteins TNF-α, TNFR1, TNFR2, ICAM1, VCAM1, and IP-10 and negatively with IL-21; also, positive associations with the anti-inflammatory proteins TGFβ1, IL-10, and IL-9 were found. Pathway enrichment analysis highlighted the involvement of sTREM2 in key functional clusters including immunoglobulin and cytokine production and cellular response to lipopolysaccharides, cytokines, and steroid hormones. Our work provides further evidence in support of TREM2 as amarker of neuroinflammatory response in AD.
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