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Prions and their lethal journey to the brain
Neil A Mabbott1, G Gordon MacPherson
1Institute for Animal Health, Ogston Building, West Mains Road, Edinburgh EH9 3JF, UK. neil.mabbott@bbsrc.ac.uk
Nature Reviews. Microbiology
|February 8, 2006
Summary
Prion diseases damage the brain. Blocking prion accumulation in lymphoid tissues reduces disease, highlighting these tissues as key for prion delivery to the brain.
Area of Science:
- Neuroscience
- Infectious Diseases
- Pathology
Background:
- Prion diseases are fatal neurodegenerative disorders.
- Prions can accumulate in lymphoid tissues before reaching the brain.
- This accumulation is crucial for efficient prion transport to the central nervous system.
Purpose of the Study:
- To review the mechanisms of prion delivery to the brain.
- To identify cellular and molecular targets for therapeutic intervention.
Main Methods:
- Literature review of studies on prion disease pathogenesis.
- Analysis of mouse models investigating prion transport.
- Examination of lymphoid tissue involvement in prion neuroinvasion.
Main Results:
- Prion accumulation in lymphoid tissues is obligatory for efficient brain delivery.
- Blocking this accumulation reduces disease susceptibility.
- Specific cells and molecules facilitate prion transport from lymphoid organs to the brain.
Conclusions:
- Understanding prion transport mechanisms is vital for developing treatments.
- Lymphoid tissues play a critical role in prion neuroinvasion.
- Targeting cellular interactions in lymphoid tissues may offer therapeutic strategies against prion diseases.

