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Summary: Latent proviruses persist in central (TCM), transitional (TTM), and effector (TEM) memory cells. We measured the levels of cellular factors involved in HIV gene expression in these subsets. The highest levels of acetylated H4, active nuclear factor κB (NF-κB), and active positive transcription elongation factor b (P-TEFb) were measured in TEM, TCM, and TTM cells, respectively. Vorinostat and romidepsin display opposite abilities to induce H4 acetylation across subsets. Protein kinase C (PKC) agonists are more efficient at inducing NF-κB phosphorylation in TCM cells but more potent at activating PTEF-b in the TEM subset. We selected the most efficient latency-reversing agents (LRAs) and measured their ability to reverse latency in each subset. While ingenol alone has modest activities in the three subsets, its combination with a histone deacetylase inhibitor (HDACi) dramatically increases latency reversal in TCM cells. Altogether, these results indicate that cellular HIV reservoirs are differentially responsive to common LRAs and suggest that combination of compounds will be required to achieve latency reversal in all subsets. : Pardons et al. measured the levels of cellular factors regulating HIV production in different memory CD4+ T cell subsets and their responsiveness to latency-reversing agents. Their results reveal that the HIV reservoir is composed of heterogenous pools of latently infected cells that differentially respond to latency-reversing agents. Keywords: HIV reservoir, latency, LRA, latency-reversing agent, memory subsets, HIV-Flow, histone acetylation, NF-κB, P-TEFb, CD4 T cells