Department of Psychiatry and Human Behavior, Brown University School of Medicine, Providence, RI, USA.
J Neuroimmunol. 2011 Apr;233(1-2):204-10. doi: 10.1016/j.jneuroim.2010.11.006. Epub 2010 Dec 10.
Cytokine disturbances have been linked to brain dysfunction among HIV-infected people. Past studies have not simultaneously examined a large set of cytokine measures and their relationships to HIV-associated neurocognitive deficits. We hypothesized that performance on measures of attention and executive and psychomotor functions would be associated with plasma cytokine concentrations in HIV-infected individuals. Plasma samples drawn from 30 HIV-infected and 37 HIV seronegative individuals were analyzed via xMAP multiplexed bead array immunoassay to determine concentrations of 13 cytokines. Performance on Trail Making A/B, Stroop Test, Letter-Number Sequencing, Digit Symbol Coding, Symbol Search, and Grooved Pegboard tests was assessed. Statistical analyses were performed to examine group differences in cytokine concentrations, and associations between cytokine and HIV clinical variables and neurocognitive performance. Significant HIV effects were found on 7 of the 13 cytokines, primarily with respect to interleukins. HIV clinical factors (CD4 and HIV RNA levels, duration of illness, antiretroviral treatment) and hepatitis C status were associated with specific plasma cytokine concentrations. Neurocognitive measures were associated with cytokine concentrations, most consistently among the interleukins and IP-10. Generally, cytokine concentrations were among the strongest predictors of neurocognitive function relative to other clinical factors, which reinforces their potential importance in examining the neuropathological processes of HIV. The findings also point to the potential value of simultaneously examining a panel of biomarkers. The current results suggest that a complex relationship likely exists among cytokines [how?] and that these relationships are mediated not only by HIV infection but also by antiretroviral treatment and other comorbid conditions.
细胞因子紊乱与 HIV 感染者的大脑功能障碍有关。过去的研究没有同时检查大量细胞因子测量及其与 HIV 相关的神经认知缺陷的关系。我们假设,注意力、执行和精神运动功能测量的表现将与 HIV 感染者的血浆细胞因子浓度相关。从 30 名 HIV 感染者和 37 名 HIV 血清阴性个体中抽取的血浆样本通过 xMAP 多重珠阵列免疫分析进行分析,以确定 13 种细胞因子的浓度。通过追踪制作 A/B、斯特鲁普测试、字母数字排序、数字符号编码、符号搜索和滚木钉板测试评估性能。进行了统计分析,以检查细胞因子浓度的组间差异,以及细胞因子与 HIV 临床变量和神经认知表现之间的关联。在 13 种细胞因子中的 7 种中发现了显著的 HIV 效应,主要与白细胞介素有关。HIV 临床因素(CD4 和 HIV RNA 水平、疾病持续时间、抗逆转录病毒治疗)和丙型肝炎状态与特定的血浆细胞因子浓度相关。神经认知测量与细胞因子浓度相关,在白细胞介素和 IP-10 中最为一致。一般来说,细胞因子浓度是相对于其他临床因素预测神经认知功能的最强指标之一,这加强了它们在检查 HIV 神经病理学过程中的潜在重要性。研究结果还表明,同时检查一组生物标志物可能具有潜在价值。目前的结果表明,细胞因子之间可能存在复杂的关系[如何?],这些关系不仅由 HIV 感染介导,而且由抗逆转录病毒治疗和其他合并症介导。