Department of Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Lebanon, NH, USA.
Division of Pharmacotherapy and Experimental Therapeutics, University of North Carolina Eshelman School of Pharmacy, Chapel Hill, NC, USA.
Sci Rep. 2017 Dec 18;7(1):17697. doi: 10.1038/s41598-017-18078-3.
HIV prevention research is focused on combining antiretrovirals (ARV) and progestin contraceptives to prevent HIV infection and pregnancy. The possibility that progestins compromise ARV anti-HIV activity prompted us to evaluate the effects of progestins on tenofovir (TFV) and TFV-alafenamide (TAF) on HIV infection and intracellular TFV-diphosphate (TFV-DP) concentrations in blood and genital CD4+ T cells. Following incubation of blood CD4+ T cells with TFV or TAF, Medroxyprogesterone acetate (MPA), but not Levonorgestrel, Norethisterone or progesterone, suppressed the anti-HIV effect of TFV by reducing intracellular TFV-DP, but had no effect on TAF inhibition of infection or TFV-DP. In contrast, with genital CD4+ T cells, MPA suppressed TAF inhibition of HIV infection and lowered of TFV-DP concentrations without affecting TFV protection. These findings demonstrate that MPA selectively compromises TFV and TAF protection in blood and genital CD4+ T cells and suggests that MPA may decrease ARV protection in individuals who use ARV intermittently for prevention.
艾滋病毒预防研究集中在将抗逆转录病毒药物 (ARV) 和孕激素避孕药结合起来,以预防艾滋病毒感染和怀孕。孕激素可能会影响 ARV 抗 HIV 活性,这促使我们评估孕激素对替诺福韦 (TFV) 和替诺福韦艾拉酚胺 (TAF) 抑制 HIV 感染和血液及生殖道 CD4+T 细胞内 TFV-二磷酸 (TFV-DP) 浓度的影响。在血液 CD4+T 细胞中孵育 TFV 或 TAF 后,醋酸甲羟孕酮(MPA)而非左炔诺孕酮、去氧孕烯或孕酮会通过减少细胞内 TFV-DP 来抑制 TFV 的抗 HIV 作用,但对 TAF 抑制感染或 TFV-DP 没有影响。相比之下,在生殖道 CD4+T 细胞中,MPA 抑制 TAF 抑制 HIV 感染并降低 TFV-DP 浓度,而不影响 TFV 保护作用。这些发现表明 MPA 选择性地损害了血液和生殖道 CD4+T 细胞中 TFV 和 TAF 的保护作用,并表明 MPA 可能会降低间断使用 ARV 进行预防的个体中 ARV 的保护作用。