首页> 外文期刊>BMC Infectious Diseases >Cerebrospinal fluid HIV-1 RNA, intrathecal immunoactivation, and drug concentrations after treatment with a combination of saquinavir, nelfinavir, and two nucleoside analogues: the M61022 study
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Cerebrospinal fluid HIV-1 RNA, intrathecal immunoactivation, and drug concentrations after treatment with a combination of saquinavir, nelfinavir, and two nucleoside analogues: the M61022 study

机译:沙奎那韦,奈非那韦和两种核苷类似物联合治疗后的脑脊液HIV-1 RNA,鞘内免疫激活和药物浓度:M61022研究

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Background The way various antiretroviral drugs and drug combinations affect HIV-1 infection in the central nervous system is still largely unknown. The aim of this study was to determine the cerebrospinal fluid (CSF) steady-state concentrations of saquinavir and nelfinavir in relation to plasma concentrations, and to study their effect in combination with two nucleoside reverse transcriptase inhibitors (NRTIs) on CSF viral loads, intrathecal immunoactivation, and blood-brain barrier integrity. Methods Paired CSF and plasma samples from 8 antiretroviral-na?ve HIV-1 infected patients starting combination therapy with saquinavir, nelfinavir, and two nucleoside analogues were collected prior to treatment, and again after approximately 12 and 48 weeks of antiretroviral therapy. Additional plasma samples were taken at weeks 2, 4, 8, 24, and 36. The concentrations of protease inhibitors were analysed, as were levels of HIV-1 RNA, CD4+ T-cell count, β2-microglobulin, neopterin, albumin ratio, IgG index, and monocytic cell count. Results None of the patients in the study presented with HIV-1 RNA Conclusion Saquinavir and nelfinavir, in combination with two NRTIs, decrease the CSF viral load and, to a lesser extent, intrathecal immunoactivation. We found reasonably high CSF concentrations of nelfinavir, but suboptimal concentrations of saquinavir.
机译:背景各种抗逆转录病毒药物和药物组合影响中枢神经系统中HIV-1感染的方式仍是未知之数。这项研究的目的是确定沙奎那韦和奈非那韦的脑脊髓液(CSF)稳态浓度与血浆浓度的关系,并研究它们与两种核苷逆转录酶抑制剂(NRTIs)联合对鞘内CSF病毒载量的影响免疫激活和血脑屏障完整性。方法在治疗前以及抗病毒治疗约12和48周后,收集开始用沙奎那韦,奈非那韦和两种核苷类似物联合治疗的8名抗逆转录病毒初次感染HIV-1的患者的配对CSF和血浆样本。在第2、4、8、24和36周时采集其他血浆样品。分析蛋白酶抑制剂的浓度,以及HIV-1 RNA的水平,CD4 + T细胞计数,β2-微球蛋白,新蝶呤,白蛋白比, IgG指数和单核细胞计数。结果研究中没有患者出现HIV-1 RNA结论结论沙奎那韦和奈非那韦与两种NRTI联合使用可降低CSF病毒载量,并在较小程度上降低鞘内免疫激活。我们发现脑脊液中的奈非那韦浓度相当高,但沙奎那韦的浓度不理想。

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