+CD38 No Differences of Immune Activation and Microbial Translocation Among HIV-infected Children Receiving Combined Antiretroviral Therapy or Protease Inhibitor Monotherapy
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No Differences of Immune Activation and Microbial Translocation Among HIV-infected Children Receiving Combined Antiretroviral Therapy or Protease Inhibitor Monotherapy

机译:在接受抗逆转录病毒疗法或蛋白酶抑制剂单一疗法联合治疗的HIV感染儿童中,免疫激活和微生物移位没有差异

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This is a cross-sectional study of 15 aviremic chronic HIV-infected children revealing no differences in immune activation (IA; HLA-DR+CD38+ CD4+ and CD8+ T cells, and sCD14) and microbial translocation (MT; lipopolysaccharides (LPS) and 16S rDNA) among HIV-infected patients under combined antiretroviral treatment (cART; n = 10) or ritonavir-boosted protease inhibitor monotherapy (mtPI/rtv; n = 5). In both cases, IA and MT were lower in healthy control children (n = 32). This observational study suggests that ritonavir boosted protease inhibitor monotherapy (mtPI/rtv) is not associated with an increased state of IA or MT as compared with children receiving cART.
机译:这是一项针对15名非HIV慢性感染性儿童的横断面研究,显示儿童的免疫激活无差异(IA; HLA-DR + CD38 + CD4 + 和CD8 + T细胞和sCD14)和微生物易位(MT ;接受抗逆转录病毒联合治疗(cART; n = 10)或利托那韦增强蛋白酶抑制剂单药治疗(mtPI / rtv; n = 5)的HIV感染患者中的脂多糖(LPS)和16S rDNA)。在这两种情况下,健康对照儿童的IA和MT均较低(n = 32)。这项观察性研究表明,与接受cART的儿童相比,利托那韦增强蛋白酶抑制剂单药治疗(mtPI / rtv)与IA或MT状态增加无关。

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