HIV感染者的自主神经病变与更密集的细胞因子网络相关。

IF 6.2
Steven Lawrence, Bridget R Mueller, Emma K T Benn, Seunghee Kim-Schulze, Patrick Kwon, Jessica Robinson-Papp
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引用次数: 0

摘要

自主神经系统(ANS)在免疫系统的调节中发挥着复杂的作用,通常通过激活免疫细胞上的β-肾上腺素受体来发挥抑制作用。我们假设HIV相关自主神经病变(HIV-AN)会导致免疫高反应性,这可以通过网络分析来描述。42名HIV控制良好的成年人接受了自主神经测试,得出综合自主神经严重程度评分(CASS)。CASS的观察范围为2-5,与正常至中度HIV-AN一致。为了构建网络,参与者根据CASS分为4组(即2、3、4或5组)。44个基于血液的免疫标记物被包括作为所有网络中的节点,并且节点对之间的连接(即边缘)由它们的二变量Spearman秩相关系数确定。计算了每个网络中每个节点的四个中心性度量(强度、接近度、介数和预期影响)。计算每个网络中所有节点的每个中心性度量的中值,作为网络复杂性的定量表示。四个网络的图形表示显示,随着HIV-AN严重程度的增加,复杂性增加。这一点得到了网络中所有四个中心性指标中值的显著差异的证实(p ≤ 每个0.025)。在HIV感染者中,HIV-AN与血液免疫标志物之间更强、更多的正相关性有关。这一二次分析的结果可用于为未来的研究提供假设,这些研究将HIV-AN作为一种有助于在HIV中观察到的慢性免疫激活的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Autonomic Neuropathy is Associated with More Densely Interconnected Cytokine Networks in People with HIV.

Autonomic Neuropathy is Associated with More Densely Interconnected Cytokine Networks in People with HIV.

The autonomic nervous system (ANS) plays a complex role in the regulation of the immune system, with generally inhibitory effects via activation of β-adrenergic receptors on immune cells. We hypothesized that HIV-associated autonomic neuropathy (HIV-AN) would result in immune hyperresponsiveness which could be depicted using network analyses. Forty-two adults with well-controlled HIV underwent autonomic testing to yield the Composite Autonomic Severity Score (CASS). The observed range of CASS was 2-5, consistent with normal to moderate HIV-AN. To construct the networks, participants were divided into 4 groups based on the CASS (i.e., 2, 3, 4 or 5). Forty-four blood-based immune markers were included as nodes in all networks and the connections (i.e., edges) between pairs of nodes were determined by their bivariate Spearman's Rank Correlation Coefficient. Four centrality measures (strength, closeness, betweenness and expected influence) were calculated for each node in each network. The median value of each centrality measure across all nodes in each network was calculated as a quantitative representation of network complexity. Graphical representation of the four networks revealed greater complexity with increasing HIV-AN severity. This was confirmed by significant differences in the median value of all four centrality measures across the networks (p ≤ 0.025 for each). Among people with HIV, HIV-AN is associated with stronger and more numerous positive correlations between blood-based immune markers. Findings from this secondary analysis can be used to generate hypotheses for future studies investigating HIV-AN as a mechanism contributing to the chronic immune activation observed in HIV.

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