Current strategies to induce selective killing of HIV‐1‐infected cells

• Published in: Journal of leukocyte biology Vol. 112; no. 5; pp. 1273 - 1284
• Main Authors: Campbell, Grant R., Spector, Stephen A.
• Format: Journal Article
• Language: English
• Published: United States 01.11.2022
• Subjects: apoptosis; autophagy; autosis; CD4-Positive T-Lymphocytes; cell death; HIV Infections; HIV-1; Humans; IAP; SMAC mimetics; Virus Latency; Virus Replication; HIV-1; autophagy; autosis; cell death; SMAC mimetics; IAP; apoptosis
• ISSN: 0741-5400; 1938-3673
• DOI: 10.1002/JLB.4MR0422-636R

Although combination antiretroviral therapy (ART) has led to significant HIV‐1 suppression and improvement in immune function, persistent viral reservoirs remain that are refractory to intensified ART. ART poses many challenges such as adherence to drug regimens, the emergence of resistant virus, and cumulative toxicity resulting from long‐term therapy. Moreover, latent HIV‐1 reservoir cells can be stochastically activated to produce viral particles despite effective ART and contribute to the rapid viral rebound that typically occurs within 2 weeks of ART interruption; thus, lifelong ART is required for continued viral suppression. Several strategies have been proposed to address the HIV‐1 reservoir such as reactivation of HIV‐1 transcription using latency reactivating agents with a combination of ART, host immune clearance and HIV‐1‐cytotoxicity to purge the infected cells—a “shock and kill” strategy. However, these approaches do not take into account the multiple transcriptional and translational blocks that contribute to HIV‐1 latency or the complex heterogeneity of the HIV‐1 reservoir, and clinical trials have thus far failed to produce the desired results. Here, we describe alternative strategies being pursued that are designed to kill selectively HIV‐1‐infected cells while sparing uninfected cells in the absence of enhanced humoral or adaptive immune responses. Graphical Overview of current strategies to kill HIV‐1‐infected cells.