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Updated: Mar 23, 2026

High Throughput In Vitro Assessment of Latency Reversing Agents on HIV Transcription and Splicing
Published on: January 22, 2019
HIV-1 Latency and Eradication: Past, Present and Future.
Prasun K Datta, Rafal Kaminski, Wenhui Hu
1Department of Neuroscience, Center for Neurovirology and Comprehensive NeuroAIDS Center, Lewis Katz School of Medicine at Temple University, 3500 N. Broad Street, 7th Floor, Philadelphia, PA 19140, USA. kamel.khalili@temple.edu.
Antiretroviral therapy (ART) controls HIV but doesn't eliminate the virus. Gene editing offers a promising strategy to inactivate latent HIV DNA, potentially leading to a cure by clearing viral reservoirs.
Area of Science:
- Virology
- Immunology
- Genetics
Background:
- Antiretroviral therapy (ART) effectively controls HIV-1 replication but cannot eliminate the virus.
- Persistent HIV-1 reservoirs, particularly in CD4+ T cells and myeloid cells, allow for viral re-emergence and progression to AIDS.
- Epigenetic modifications, including chromatin structure, are implicated in establishing and maintaining HIV-1 latency.
Purpose of the Study:
- To explore novel strategies for eradicating persistent HIV-1 reservoirs.
- To investigate the potential of gene editing technology for eliminating latent proviral DNA.
Main Methods:
- Review of current HIV-1 eradication approaches, including 'shock and kill' strategies.
- Examination of recent advances in gene editing technologies for targeting integrated proviral DNA.
Main Results:
- The 'shock and kill' approach faces limitations requiring further investigation for clinical application.
- Gene editing presents a powerful potential strategy for inactivating latent HIV-1 proviral DNA.
Conclusions:
- Eliminating the latent HIV-1 reservoir is crucial for achieving a functional cure.
- Gene editing technology, with further development in understanding viral genetics and delivery, holds promise for eradicating latent HIV-1 and achieving a sterile cure for AIDS.
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