Selective BCL-XLAntagonists Eliminate Infected Cells from a Primary Cell Model of HIV Latency but not from Ex Vivo Reservoirs

HIV persists, despite antiviral immune responses and effective antiretroviral therapy, in viral reservoirs that seed rebound viremia if therapy is interrupted. Previously, we showed that the BCL-2 protein contributes to HIV persistence by conferring a survival advantage to reservoir-harboring cells. Here, we demonstrate that many of the BCL-2 family members  are overexpressed in HIV-infected CD4 + T-cells, indicating increased tension between pro-apoptotic and pro-survival familymembers – as well as raising the possibility that the inhibition of pro-survival members may disproportionately affect the survival of HIV-infected cells. Based on these results, we chose to further study  BCL2L1 (encoding the protein BCL-X L ), due to its consistent overexpression and the availability of selective antagonists. Infection of primary CD4 + T-cells with either a clinical isolate, a CCR5-tropic strain, or a CXCR4-tropic strain of HIV resulted in increased BCL-X L protein expression; and treatment with two selective BCL-X L antagonists, A-1155463 and A-1551852, led to disproportionate cell death compared to uninfected CD4 + T-cells. In a primary cell model of latency, both BCL-X L antagonists drove significant reductions in total HIV DNA and in infectious cell frequencies both alone and in combination with the latency reversing agent bryostatin-1, with little off-target cytotoxicity. However, these antagonists, with or without bryostatin-1, or in combination with the highly potent latency reversing agent combination PMA + ionomycin, failed to reduce total HIV DNA and infectious reservoirs in  ex vivo CD4 + T-cells from ART-suppressed donors. Our results add to growing evidence that bonafide reservoir-harboring cells are resistant to multiple “kick and kill” modalities - relative to latency models - and uncover BCL-X L antagonists as a facile approach to probing mechanistic underpinnings. We also interpret our results as encouraging of further exploration of BCL-X L antagonists for cure, where combination approaches may unlock the ability to eliminate  ex vivo  reservoirs.