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Sci Adv ; 9(11): eade6675, 2023 03 17.
Article in English | MEDLINE | ID: mdl-36921041

ABSTRACT

Reactivation of the latent HIV-1 reservoir is a first step toward triggering reservoir decay. Here, we investigated the impact of the BAF complex inhibitor pyrimethamine on the reservoir of people living with HIV-1 (PLWH). Twenty-eight PLWH on suppressive antiretroviral therapy were randomized (1:1:1:1 ratio) to receive pyrimethamine, valproic acid, both, or no intervention for 14 days. The primary end point was change in cell-associated unspliced (CA US) HIV-1 RNA at days 0 and 14. We observed a rapid, modest, and significant increase in (CA US) HIV-1 RNA in response to pyrimethamine exposure, which persisted throughout treatment and follow-up. Valproic acid treatment alone did not increase (CA US) HIV-1 RNA or augment the effect of pyrimethamine. Pyrimethamine treatment did not result in a reduction in the size of the inducible reservoir. These data demonstrate that the licensed drug pyrimethamine can be repurposed as a BAF complex inhibitor to reverse HIV-1 latency in vivo in PLWH, substantiating its potential advancement in clinical studies.


Subject(s)
HIV Infections , HIV-1 , Humans , CD4-Positive T-Lymphocytes , HIV Infections/drug therapy , HIV-1/physiology , Pyrimethamine/pharmacology , Pyrimethamine/therapeutic use , RNA , Valproic Acid/pharmacology , Virus Activation , Virus Latency
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