Department of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium.
Liver Research Centre Ghent, Ghent University, Ghent, Belgium.
J Interferon Cytokine Res. 2024 Aug;44(8):372-378. doi: 10.1089/jir.2024.0053. Epub 2024 Jun 27.
The study of sensitive and specific biomarkers, such as blood inflammatory cytokines, could provide an answer to the challenges faced in the differential diagnosis of patients with systemic inflammation. Limited data exist on the impact of age on serum levels of inflammatory cytokines. We collected serum samples of 42 healthy children and young adults (1 month to 21 years). Serum levels of interleukin 1 receptor antagonist (IL-1Ra), IL-1β, IL-6, IL-18, tumor necrosis factor-alpha (TNF-α), CXCL9, and CXCL10 were measured. Data were analyzed for three different age groups (<6, 6-17, and 18-21 years). IL-18, TNF-α, and CXCL9 values varied significantly according to age group. Median values of IL-18 and TNF-α decline with age, whereas CXCL9 and CXCL10 are lowest at 6-17 years. IL-1Ra is stable among age groups. In the majority of cases, IL-1β and IL-6 are not measurable above the lower limit of quantification. A scoping literature review revealed highly variable data on IL-1Ra, IL-18, TNF-α, and CXCL10. For CXCL9, pediatric reference data are scarce. In conclusion, we report an age-dependent signature of multiple inflammatory cytokines measured in the serum of healthy children and young adults, suggesting the need to use age-specific reference values in future pediatric studies.
这项研究关注敏感和特异性生物标志物,如血液炎症细胞因子,这可能为系统炎症患者的鉴别诊断提供答案。目前关于年龄对炎症细胞因子血清水平影响的数据有限。我们收集了 42 名健康儿童和年轻人(1 个月至 21 岁)的血清样本。测量了白细胞介素 1 受体拮抗剂(IL-1Ra)、IL-1β、IL-6、IL-18、肿瘤坏死因子-α(TNF-α)、CXCL9 和 CXCL10 的血清水平。数据根据三个不同年龄组(<6 岁、6-17 岁和 18-21 岁)进行分析。IL-18、TNF-α和 CXCL9 的值根据年龄组有显著差异。IL-18 和 TNF-α 的中位数随年龄下降,而 CXCL9 和 CXCL10 在 6-17 岁时最低。IL-1Ra 在各年龄组之间保持稳定。在大多数情况下,IL-1β和 IL-6 的测量值低于定量下限。范围文献综述显示,IL-1Ra、IL-18、TNF-α和 CXCL10 的数据差异很大。对于 CXCL9,儿科参考数据稀缺。总之,我们报告了健康儿童和年轻人血清中多种炎症细胞因子的年龄依赖性特征,这表明在未来的儿科研究中需要使用特定年龄的参考值。