Advancements in single-cell techniques for examining the HIV reservoir: pathways to a cure
2025
Nokuzola Mbhele | Benjamin Chimukangara | Lynn Tyers | Frank Maldarelli | Andrew D. Redd
ABSTRACT Human immunodeficiency virus (HIV) is largely incurable, due to the presence of a viral reservoir, which primarily consists of resting CD4+ T cells and other long-lived cells like macrophages. These reservoir cells, which persist despite suppressive antiretroviral therapy (ART), are thought to be influenced by several key factors such as position and orientation of chromosomal proviral integration, proviral intactness, and antigen specificity. The host’s immune status and immune selection pressures also likely play a significant role. Recent data suggest that the HIV provirus integrates into specific chromosomal regions, such as centromeric areas with low RNA expression, allowing the virus to evade detection. To effectively disrupt HIV latency, enhance immune recognition, and eliminate reservoir cells, a precise understanding of these viral reservoirs at single-cell level will be crucial. Gaining insights into the unique characteristics of these reservoir cells, including data on integration sites and gene expression profiles, is essential for designing targeted interventions. This review highlights current single-cell approaches, including single-cell sequencing, chromatin accessibility assays, and multiomic techniques, as tools for uncovering the heterogeneity and resilience of HIV reservoirs. Taken together, these methods aim to reveal the complexities of the HIV reservoir and promote the development of novel therapeutic strategies.
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