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PolyIC-coated Prussian blue nanoparticles as a dual-mode HIV latency reversing agent
Preethi B Balakrishnan1,2, Carissa S Holmberg3,4, Debbie K Ledezma1,2,3
1Department of Medicine, The George Washington University, 2300 I Street NW, Washington, DC 20037, USA.
Nanomedicine (London, England)
|February 3, 2023
Summary
Prussian blue nanoparticles (PBNPs) coated with polyinosinic-polycytidylic acid (polyIC) effectively reverse HIV latency. These polyIC-PBNPs also enhance immune activation in T cells, showing promise for HIV therapy.
Area of Science:
- Nanomedicine
- Virology
- Immunology
Background:
- Human Immunodeficiency Virus (HIV) establishes latent reservoirs, complicating eradication efforts.
- Reactivating latent HIV is a key strategy for potential therapeutic interventions.
- Developing effective delivery systems for latency-reversing agents is crucial.
Purpose of the Study:
- To synthesize and evaluate Prussian blue nanoparticles (PBNPs) coated with polyinosinic-polycytidylic acid (polyIC).
- To determine the efficacy of polyIC-PBNPs as HIV latency reversing agents.
- To assess the impact of polyIC-PBNPs on immune activation.
Main Methods:
- PolyIC-PBNPs were synthesized using a layer-by-layer method.
- Characterization confirmed nanoparticle stability, monodispersity, and efficient polyIC attachment.
- Cell models of HIV latency were used to assess HIV reactivation and immune cell activation.
Main Results:
- PolyIC-PBNPs demonstrated superior HIV latency reversal compared to free polyIC.
- Enhanced immune activation was observed in CD4 and CD8 T cells treated with polyIC-PBNPs.
- The synthesized polyIC-PBNPs maintained essential properties of both polyIC and PBNPs.
Conclusions:
- Prussian blue nanoparticles serve as effective carriers for nucleic acids like polyIC.
- PolyIC-PBNPs can directly reverse HIV latency.
- This approach also enhances immune activation, offering a dual therapeutic benefit for HIV treatment.

