Target intelligence / Profile preview

Integrated Human Immunodeficiency Virus proviral DNA (HIV proviral DNA) (HIV proviral DNA)

Target
HIV proviral DNA
Molecular classification
Nucleic acid, Viral genome
01

Overview

Integrated Human Immunodeficiency Virus (HIV) proviral DNA is the double-stranded DNA sequence synthesized from the viral RNA genome and subsequently inserted into the host cell's nuclear DNA (PMID: 30696983). This integration is a defining step in the HIV life cycle, mediated by the viral enzyme integrase, and establishes a permanent infection within the host (PMID: 22835941). The provirus serves as the template for all subsequent viral transcription and replication; however, in a subset of cells, it enters a latent state where it remains transcriptionally silent and invisible to the immune system (PMID: 25241201). This latent reservoir is the primary barrier to a definitive cure, as it persists despite suppressive antiretroviral therapy (ART) and can spontaneously reactivate (PMID: 26351141). Therapeutic interventions targeting the provirus include latency-reversing agents (LRAs) to induce viral expression for immune-mediated clearance, transcriptional inhibitors to enforce permanent silencing, and gene-editing tools like CRISPR/Cas9 to physically excise the viral sequence (NCT05144386). Monitoring the proviral reservoir is typically achieved through specialized assays like the Intact Proviral DNA Assay (IPDA), which distinguishes between defective and replication-competent proviruses (PMID: 30696983). Successfully targeting and eliminating or permanently silencing integrated proviral DNA is considered the primary goal for achieving a functional or sterilizing cure for HIV/AIDS.

Other names
HIV provirusIntegrated HIV-1 DNALatent HIV reservoirHIV-1 proviral DNA
02

Mechanism of action

Therapeutic strategies include latency reversal (shock and kill) using HDAC inhibitors to induce viral expression, transcriptional silencing (block and lock) to permanently suppress the provirus, and direct excision using gene-editing technologies like CRISPR/Cas9 (PMID: 22835941, PMID: 30696983, NCT05144386).

03

Biological functions

Viral replicationViral latencyGenomic integration
04

Disease associations

Infection
05

Safety considerations

Off-target genomic mutations from gene-editing toolsSystemic toxicity and global gene activation from latency-reversing agentsImmune exhaustion or cytokine stormPotential for oncogenesis if host tumor suppressor genes are disrupted
06

Interacting drugs

Vorinostat

6 more in the full profile.

07

Biomarkers

Intact Proviral DNA Assay (IPDA)Cell-associated HIV RNA (ca-RNA)Total HIV DNAQuantitative Viral Outgrowth Assay (QVOA)Tat/rev Induced Limiting Dilution Assay (TILDA)

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