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Cell-based Assay to Study Antibody-mediated Tau Clearance by Microglia
Published on: November 9, 2018
Time to test antibacterial therapy in Alzheimer's disease
Francesco Panza1, Madia Lozupone1,2, Vincenzo Solfrizzi3
1Unit of Epidemiological Research on Aging, National Institute of Gastroenterology 'Saverio de Bellis', Research Hospital, Castellana Grotte, Bari, Italy.
Abstract:
Alzheimer's disease is associated with cerebral accumulation of amyloid-β peptide and hyperphosphorylated tau. In the past 28 years, huge efforts have been made in attempting to treat the disease by reducing brain accumulation of amyloid-β in patients with Alzheimer's disease, with no success. While anti-amyloid-β therapies continue to be tested in prodromal patients with Alzheimer's disease and in subjects at risk of developing Alzheimer's disease, there is an urgent need to provide therapeutic support to patients with established Alzheimer's disease for whom current symptomatic treatment (acetylcholinesterase inhibitors and N-methyl d-aspartate antagonist) provide limited help. The possibility of an infectious aetiology for Alzheimer's disease has been repeatedly postulated over the past three decades. Infiltration of the brain by pathogens may act as a trigger or co-factor for Alzheimer's disease, with Herpes simplex virus type 1, Chlamydia pneumoniae, and Porphyromonas gingivalis being most frequently implicated. These pathogens may directly cross a weakened blood-brain barrier, reach the CNS and cause neurological damage by eliciting neuroinflammation. Alternatively, pathogens may cross a weakened intestinal barrier, reach vascular circulation and then cross blood-brain barrier or cause low grade chronic inflammation and subsequent neuroinflammation from the periphery. The gut microbiota comprises a complex community of microorganisms. Increased permeability of the gut and blood-brain barrier induced by microbiota dysbiosis may impact Alzheimer's disease pathogenesis. Inflammatory microorganisms in gut microbiota are associated with peripheral inflammation and brain amyloid-β deposition in subjects with cognitive impairment. Oral microbiota may also influence Alzheimer's disease risk through circulatory or neural access to the brain. At least two possibilities can be envisaged to explain the association of suspected pathogens and Alzheimer's disease. One is that patients with Alzheimer's disease are particularly prone to microbial infections. The other is that microbial infection is a contributing cause of Alzheimer's disease. Therapeutic trials with antivirals and/or antibacterials could resolve this dilemma. Indeed, antiviral agents are being tested in patients with Alzheimer's disease in double-blind placebo-controlled studies. Although combined antibiotic therapy was found to be effective in animal models of Alzheimer's disease, antibacterial drugs are not being widely investigated in patients with Alzheimer's disease. This is because it is not clear which bacterial populations in the gut of patients with Alzheimer's disease are overexpressed and if safe, selective antibacterials are available for them. On the other hand, a bacterial protease inhibitor targeting P. gingivalis toxins is now being tested in patients with Alzheimer's disease. Clinical studies are needed to test if countering bacterial infection may be beneficial in patients with established Alzheimer's disease.
Insights
Investigating the infectious origins of Alzheimer's disease (AD) is crucial. Emerging evidence suggests pathogens and gut microbiota dysbiosis may contribute to AD, necessitating new therapeutic strategies beyond amyloid-beta reduction.
Area of Science:
- Neuroscience
- Infectious Diseases
- Microbiology
Background:
- Alzheimer's disease (AD) is characterized by amyloid-beta and tau pathology, but anti-amyloid therapies have shown limited success.
- Current symptomatic treatments for AD offer minimal benefit to patients with established disease.
- An infectious etiology for AD has been proposed, implicating pathogens like Herpes simplex virus type 1, Chlamydia pneumoniae, and Porphyromonas gingivalis.
Purpose of the Study:
- To explore the potential role of infectious agents and gut microbiota dysbiosis in Alzheimer's disease pathogenesis.
- To highlight the urgent need for alternative therapeutic approaches for established Alzheimer's disease.
- To discuss the implications of pathogen infiltration via weakened blood-brain or intestinal barriers.
Main Methods:
- Review of existing literature on Alzheimer's disease, infectious agents, and gut microbiota.
- Analysis of proposed mechanisms for pathogen entry into the central nervous system (CNS).
- Discussion of the impact of gut-brain axis dysregulation on neuroinflammation and amyloid-beta deposition.
Main Results:
- Pathogens may trigger or co-factor AD by directly crossing the blood-brain barrier or causing peripheral inflammation.
- Gut microbiota dysbiosis can increase intestinal and blood-brain barrier permeability, influencing AD pathogenesis.
- Inflammatory gut microbes are linked to peripheral inflammation and amyloid-beta deposition in cognitive impairment.
Conclusions:
- Infectious agents and gut dysbiosis represent potential contributing factors to Alzheimer's disease.
- Antiviral and antibacterial therapies warrant further investigation as potential treatments for AD.
- Clinical trials are needed to determine the efficacy of targeting infections in patients with established Alzheimer's disease.
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