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NF-κB sub-pathways and HIV cure: A revisit.
1UNC HIV Cure Center, Institute of Global Health and Infectious Diseases, United States.
Ebiomedicine
|December 19, 2020
Summary
This review explores strategies for an HIV cure by targeting Nuclear Factor kappa B (NF-κB) signaling pathways. Understanding NF-κB sub-pathways offers new avenues to disrupt latent HIV reservoirs and achieve a functional cure.
Area of Science:
- Virology
- Immunology
- Molecular Biology
Background:
- Human Immunodeficiency Virus (HIV) cure remains elusive due to latent reservoirs.
- Antiretroviral Therapy (ART) suppresses but does not eradicate HIV.
- Reactivation of latent HIV leads to viral rebound after ART cessation.
Purpose of the Study:
- To review curative strategies for HIV focusing on NF-κB signaling pathways.
- To explore the role of canonical and noncanonical NF-κB signaling in HIV latency reversal.
- To identify novel upstream signaling pathways of NF-κB for HIV functional cure.
Main Methods:
- Literature review of existing research on HIV cure strategies.
- Analysis of NF-κB signaling pathways and their impact on HIV latency.
- Exploration of upstream regulators of NF-κB in the context of HIV.
Main Results:
- Canonical NF-κB signaling is known to induce HIV proviral expression.
- Noncanonical NF-κB signaling also promotes HIV expression from latency.
- Novel upstream signaling pathways of NF-κB present new therapeutic targets.
Conclusions:
- Targeting NF-κB sub-pathways shows promise for disrupting latent HIV.
- Both canonical and noncanonical NF-κB pathways are implicated in HIV latency reversal.
- Investigating upstream NF-κB signaling may lead to a functional HIV cure.
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