对支气管肺泡灌洗液和血浆进行高度多重细胞因子分析,揭示了与年龄相关的儿童炎症动态和相关因素。

Shivanthan Shanthikumar, Liam Gubbels, Karen Davies, Hannah Walker, Anson Tsz Chun Wong, Eric Levi, Richard Saffery, Sarath C. Ranganathan, Melanie R. Neeland
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引用次数: 0

摘要

尽管细胞因子在一系列儿童疾病的炎症介导过程中起着核心作用,但细胞因子检测仍主要局限于研究环境,炎症的替代标记物通常用于为临床诊断和治疗决策提供依据。目前还没有健康儿童全身(血液)或疾病部位(如肺部)细胞因子的参考范围。在我们的研究中,我们的目标是为 1-16 岁健康儿童的呼吸道和血液中的细胞因子建立一个可公开获取的参考值。我们研究了细胞因子浓度在儿童时期的变化情况,并评估了一套核心的细胞因子标记物是否可用于间接评估各种炎症分析物的反应。为了开发我们的参考指标,我们在 78 名儿童的无细胞支气管肺泡灌洗液(BAL)和血浆中测量了共 78 种独特的分析物。我们的研究表明,年龄对这两种样本中的可溶性免疫分析物浓度都有很大影响,并确定了一组高度相关的核心分析物,包括 BAL 中的 10 种分析物和血浆中的 11 种分析物,能够间接评估多达 34 种炎症介质的反应。这项研究满足了为健康儿童制定细胞因子参考范围的迫切需要,以帮助诊断疾病、确定细胞因子靶向单克隆抗体疗法的资格并监测其效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Highly multiplexed cytokine analysis of bronchoalveolar lavage and plasma reveals age-related dynamics and correlates of inflammation in children.
Despite the central role of cytokines in mediating inflammation that underlies a range of childhood diseases, cytokine testing remains primarily limited to research settings and surrogate markers of inflammation are often used to inform clinical diagnostic and treatment decisions. There are currently no reference ranges available for cytokines in healthy children, either systemically (in blood) or at sites of disease (such as the lung). In our study, we aimed to develop an openly accessible reference of cytokines in the airways and blood of healthy children spanning 1 to 16 years of age. We examined how cytokine concentration changes during childhood and assessed whether a core set of cytokine markers could be used to indirectly evaluate the response of a broad spectrum of inflammatory analytes. To develop our reference, a total of 78 unique analytes were measured in cell-free bronchoalveolar lavage (BAL) and plasma from 78 children. We showed that age profoundly impacts soluble immune analyte concentration in both sample types and identified a highly correlative core set of 10 analytes in BAL and 11 analytes in plasma capable of indirectly evaluating the response of up to 34 inflammatory mediators. This study addresses an urgent need to develop reference ranges for cytokines in healthy children to aid in diagnosis of disease, to determine eligibility for, and to monitor the effects of, cytokine-targeted monoclonal antibody therapy.
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