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脑脊液中的趋化因子与 HIV 感染个体的大脑代谢物模式相关。

Chemokines in cerebrospinal fluid correlate with cerebral metabolite patterns in HIV-infected individuals.

机构信息

University of California, San Diego, 220 Dickinson Street, Suite A, San Diego, CA 92103, USA.

出版信息

J Neurovirol. 2011 Feb;17(1):63-9. doi: 10.1007/s13365-010-0013-2. Epub 2011 Jan 19.

Abstract

Chemokines influence HIV neuropathogenesis by affecting the HIV life cycle, trafficking of macrophages into the nervous system, glial activation, and neuronal signaling and repair processes; however, knowledge of their relationship to in vivo measures of cerebral injury is limited. The primary objective of this study was to determine the relationship between a panel of chemokines in cerebrospinal fluid (CSF) and cerebral metabolites measured by proton magnetic resonance spectroscopy (MRS) in a cohort of HIV-infected individuals. One hundred seventy-one stored CSF specimens were assayed from HIV-infected individuals who were enrolled in two ACTG studies that evaluated the relationship between neuropsychological performance and cerebral metabolites. Concentrations of six chemokines (fractalkine, IL-8, IP-10, MCP-1, MIP-1β, and SDF-1) were measured and compared with cerebral metabolites individually and as composite neuronal, basal ganglia, and inflammatory patterns. IP-10 and MCP-1 were the chemokines most strongly associated with individual cerebral metabolites. Specifically, (1) higher IP-10 levels correlated with lower N-acetyl aspartate (NAA)/creatine (Cr) ratios in the frontal white matter and higher MI/Cr ratios in all three brain regions considered and (2) higher MCP-1 levels correlated with lower NAA/Cr ratios in frontal white matter and the parietal cortex. IP-10, MCP-1, and IL-8 had the strongest associations with patterns of cerebral metabolites. In particular, higher levels of IP-10 correlated with lower neuronal pattern scores and higher basal ganglia and inflammatory pattern scores, the same pattern which has been associated with HIV-associated neurocognitive disorders (HAND). Subgroup analysis indicated that the effects of IP-10 and IL-8 were influenced by effective antiretroviral therapy and that memantine treatment may mitigate the neuronal effects of IP-10. This study supports the role of chemokines in HAND and the validity of MRS as an assessment tool. In particular, the findings identify relationships between the immune response-particularly an interferon-inducible chemokine, IP-10-and cerebral metabolites and suggest that antiretroviral therapy and memantine modify the impact of the immune response on neurons.

摘要

趋化因子通过影响 HIV 生命周期、巨噬细胞向神经系统的转移、神经胶质细胞的激活以及神经元信号和修复过程来影响 HIV 神经发病机制;然而,它们与体内脑损伤测量值之间的关系知之甚少。本研究的主要目的是确定一组脑脊液(CSF)趋化因子与通过质子磁共振波谱(MRS)测量的 HIV 感染个体脑代谢物之间的关系。从参加两项评估神经心理表现与脑代谢物关系的 ACTG 研究的 HIV 感染者中,检测了 171 份储存的 CSF 标本。测量了六种趋化因子( fractalkine、IL-8、IP-10、MCP-1、MIP-1β 和 SDF-1)的浓度,并分别比较了脑代谢物以及神经元、基底神经节和炎症复合模式。IP-10 和 MCP-1 是与个体脑代谢物最相关的趋化因子。具体来说,(1)较高的 IP-10 水平与额白质中 N-乙酰天冬氨酸(NAA)/肌酸(Cr)比值降低和所有三个脑区的 MI/Cr 比值升高相关;(2)较高的 MCP-1 水平与额白质和顶叶皮层中 NAA/Cr 比值降低相关。IP-10、MCP-1 和 IL-8 与脑代谢物模式的相关性最强。特别是,较高的 IP-10 水平与较低的神经元模式评分和较高的基底神经节和炎症模式评分相关,这种模式与 HIV 相关认知障碍(HAND)相关。亚组分析表明,IP-10 和 IL-8 的作用受有效抗逆转录病毒治疗的影响,而美金刚治疗可能减轻 IP-10 对神经元的影响。这项研究支持趋化因子在 HAND 中的作用以及 MRS 作为评估工具的有效性。特别是,研究结果确定了免疫反应(特别是干扰素诱导的趋化因子 IP-10)与脑代谢物之间的关系,并表明抗逆转录病毒治疗和美金刚可改变免疫反应对神经元的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6631/3032187/8f9651d75316/13365_2010_13_Fig1_HTML.jpg

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