Innate Immunity Stimulation via Toll-Like Receptor 9 Ameliorates Vascular Amyloid Pathology in Tg-SwDI Mice with Associated Cognitive Benefits.
Henrieta ScholtzovaEileen DoShleshma DhakalYanjie SunShan LiuPankaj D MehtaThomas M WisniewskiPublished in: The Journal of neuroscience : the official journal of the Society for Neuroscience (2017)
Recent genetic studies have underscored the emerging role of microglia in Alzheimer's disease (AD) pathogenesis. Microglia lose their amyloid-β-clearing capabilities with age and as AD progresses. Therefore, the ability to modulate microglia profiles offers a promising therapeutic avenue for reducing AD pathology. Current immunotherapeutic approaches have been limited by poor clearance of a core AD lesion, cerebral amyloid angiopathy (CAA). The present study used Tg-SwDI mice, which have extensive CAA. We found that stimulation of the innate immune system and microglia/macrophage activation via Toll-like receptor 9 using CpG (cytosine-phosphate-guanine) oligodeoxynucleotides (ODNs) leads to cognitive improvements and CAA reduction, without associated toxicity. Our data indicate that this novel concept of immunomodulation represents a safer method to reduce all aspects of AD pathology and provide essential information for potential clinical use of CpG ODN.
Keyphrases
- toll like receptor
- inflammatory response
- immune response
- nuclear factor
- neuropathic pain
- dna methylation
- high fat diet induced
- adipose tissue
- oxidative stress
- genome wide
- cognitive decline
- electronic health record
- gene expression
- subarachnoid hemorrhage
- spinal cord injury
- metabolic syndrome
- machine learning
- spinal cord
- big data
- artificial intelligence