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JC Polyomavirus Attachment and Entry: Potential Sites for PML Therapeutics
Colleen L Mayberry1, Christian D S Nelson2, Melissa S Maginnis1,3
1Department of Molecular and Biomedical Sciences, The University of Maine, Orono, ME, USA.
JC polyomavirus (JCPyV) causes progressive multifocal leukoencephalopathy (PML) in immunosuppressed individuals. Targeting JCPyV attachment and entry offers promising therapeutic strategies for this fatal disease.
Area of Science:
- Virology
- Immunology
- Neuroscience
Background:
- JC polyomavirus (JCPyV) establishes asymptomatic kidney infections in most people.
- Reactivation in immunocompromised individuals leads to fatal progressive multifocal leukoencephalopathy (PML).
- Limited therapeutic options exist for PML.
Purpose of the Study:
- To review current knowledge of JCPyV attachment and entry mechanisms.
- To explore potential therapeutic targets for preventing or treating PML by inhibiting these initial steps.
Main Methods:
- Literature review of JCPyV infection pathways.
- Analysis of host-pathogen interactions.
- Evaluation of emerging therapeutic strategies.
Main Results:
- JCPyV utilizes α2,6-linked lactoseries tetrasaccharide c (LSTc) for attachment and 5-hydroxytryptamine receptors (5-HT2Rs) for entry.
- Endoplasmic reticulum trafficking is essential for JCPyV infection.
- Vaccines, monoclonal antibodies, and small molecules show therapeutic potential.
Conclusions:
- Understanding JCPyV attachment, entry, and trafficking is crucial for PML therapeutic development.
- Targeting these viral processes presents a viable strategy for combating PML.
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