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Latency reversal plus natural killer cells diminish HIV reservoir in vivo.

Jocelyn T KimTian-Hao ZhangCamille CarmonaBryanna LeeChristopher S SeetMatthew KostelnyNisarg ShahHongying ChenKylie FarrellMohamed S A SolimanMelanie DimapasocMichelle SinaniKenia Yazmin Reyna BlancoDavid BojorquezHong JiangYuan ShiYushen DuNatalia L KomarovaDominik WodarzPaul A WenderMatthew D MarsdenRen SunJerome A Zack
Published in: Nature communications (2022)
HIV is difficult to eradicate due to the persistence of a long-lived reservoir of latently infected cells. Previous studies have shown that natural killer cells are important to inhibiting HIV infection, but it is unclear whether the administration of natural killer cells can reduce rebound viremia when anti-retroviral therapy is discontinued. Here we show the administration of allogeneic human peripheral blood natural killer cells delays viral rebound following interruption of anti-retroviral therapy in humanized mice infected with HIV-1. Utilizing genetically barcoded virus technology, we show these natural killer cells efficiently reduced viral clones rebounding from latency. Moreover, a kick and kill strategy comprised of the protein kinase C modulator and latency reversing agent SUW133 and allogeneic human peripheral blood natural killer cells during anti-retroviral therapy eliminated the viral reservoir in a subset of mice. Therefore, combinations utilizing latency reversal agents with targeted cellular killing agents may be an effective approach to eradicating the viral reservoir.
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