Department of Physiology and Neurobiology, Geisel School of Medicine at Dartmouth, Lebanon, New Hampshire, United States of America.
PLoS One. 2013 Oct 25;8(10):e78814. doi: 10.1371/journal.pone.0078814. eCollection 2013.
Tenofovir (TFV) has been widely used for pre-exposure prophylaxis of HIV-1 infection with mixed results. While the use of TFV in uninfected individuals for prevention of HIV-1 acquisition is actively being investigated, the possible consequences of TFV exposure for the HIV-target cells and the mucosal microenvironment are unknown. In the current study, we evaluated the effects of TFV treatment on blood-derived CD4⁺ T cells, monocyte-derived macrophages and dendritic cells (DC). Purified HIV-target cells were treated with different concentrations of TFV (0.001-1.0 mg/ml) for 2 to 24 hr. RNA was isolated and RT-PCR was performed to compare the levels of mRNA expression of nucleotidases and pro-inflammatory cytokine genes (MIP3α, IL-8 and TNFα) in the presence or absence of TFV. We found that TFV increases 5'-ecto-nucleotidase (NT5E) and inhibits mitochondrial nucleotidase (NT5M) gene expression and increases 5' nucleotidase activity in macrophages. We also observed that TFV stimulates the expression and secretion of IL-8 by macrophages, DC, and activated CD4⁺ T cells and increases the expression and secretion of MIP3α by macrophages. In contrast, TFV had no effect on TNFα secretion from macrophages, DC and CD4⁺ T cells. Our results demonstrate that TFV alters innate immune responses in HIV-target cells with potential implications for increased inflammation at mucosal surfaces. As new preventive trials are designed, these findings should provide a foundation for understanding the effects of TFV on HIV-target cells in microbicide trials.
替诺福韦(TFV)已被广泛用于预防 HIV-1 感染,但效果不一。目前正在积极研究将 TFV 用于未感染人群以预防 HIV-1 感染,然而 TFV 暴露对 HIV 靶细胞和黏膜微环境的可能影响尚不清楚。在本研究中,我们评估了 TFV 治疗对血液来源的 CD4 ⁺ T 细胞、单核细胞衍生的巨噬细胞和树突状细胞(DC)的影响。用不同浓度的 TFV(0.001-1.0mg/ml)处理纯化的 HIV 靶细胞 2 至 24 小时。分离 RNA 并进行 RT-PCR,以比较在存在或不存在 TFV 的情况下核酶和促炎细胞因子基因(MIP3α、IL-8 和 TNFα)的 mRNA 表达水平。我们发现 TFV 增加了 5'-外切核苷酸酶(NT5E)和抑制了线粒体核苷酸酶(NT5M)的基因表达,并增加了巨噬细胞中的 5' 核苷酸酶活性。我们还观察到 TFV 刺激了巨噬细胞、DC 和活化的 CD4 ⁺ T 细胞中 IL-8 的表达和分泌,并增加了巨噬细胞中 MIP3α 的表达和分泌。相比之下,TFV 对巨噬细胞、DC 和 CD4 ⁺ T 细胞中 TNFα 的分泌没有影响。我们的结果表明,TFV 改变了 HIV 靶细胞中的固有免疫反应,这可能增加了黏膜表面的炎症。随着新的预防试验的设计,这些发现应为理解微生态制剂试验中 TFV 对 HIV 靶细胞的影响提供基础。