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监测疑似或确诊感染的足月新生儿淋巴细胞亚群和前炎症介质的变化。

Tracking changes of lymphocyte subsets and pre-inflammatory mediators in full-term neonates with suspected or documented infection.

机构信息

Neonatal Intensive Care Unit, University Hospital of Ioannina, Ioannina, Leoforos Stavrou Niarchou, Greece.

出版信息

Scand J Immunol. 2011 Mar;73(3):250-5. doi: 10.1111/j.1365-3083.2010.02499.x.

DOI:10.1111/j.1365-3083.2010.02499.x
PMID:21204898
Abstract

Investigation was made of changes in immune system parameters during the course of neonatal infection. The study population consisted of 95 full-term neonates matched for chronological age and sex, divided into three groups: suspected infection (n=20), sepsis (n=25), infection-free control subjects (n=50). Serial measurements were made of the cytokines interleukin-6 (IL-6), interleukin-1b (IL-1b) and tumour necrosis factor-α (TNF-α), lymphocyte subsets [CD3+, CD4+, CD8+, natural killer (NK) cells and B cells], the immunoglobulins (Ig) (IgG, IgM and IgA), C-reactive protein (CRP), and the total blood count, before, 2 days after initiation of treatment and after stopping treatment (time periods first, second and third, respectively). IL6, TNF-α, IL1-b and CRP were higher at the first time period in the sepsis group, and IL6 and TNF-α continued to be higher in this group at the second period. IL-6 and TNF-α were precise sepsis predictors with sensitivity and specificity of 0.92, 0.98 and 0.91, 0.92, respectively. NK cells, B cells, CD3+, CD4+, CD8+ were higher in the sepsis and suspected infection groups, but the ratios CD3+/CD4+, CD3+/CD8+, CD4+/CD8+ showed no difference from the controls. IgG was lower and IgM higher in the sepsis group. In the control subjects CD3+, CD4+, CD8+ lymphocytes increased with increasing age. It is concluded that IL-6 and TNF are good diagnostic markers of sepsis in full-term neonates. Lymphocyte subsets were affected by both the clinical condition and the chronological age. NK and B cells may be elevated in suspected and documented sepsis, and further studies are needed to determine their clinical significance.

摘要

研究了新生儿感染过程中免疫系统参数的变化。研究人群由 95 名按时间顺序年龄和性别匹配的足月新生儿组成,分为三组:疑似感染(n=20)、败血症(n=25)和无感染对照(n=50)。在开始治疗前、治疗后 2 天和停止治疗后(分别为第一、第二和第三时间段),连续测量细胞因子白细胞介素-6(IL-6)、白细胞介素-1b(IL-1b)和肿瘤坏死因子-α(TNF-α)、淋巴细胞亚群[CD3+、CD4+、CD8+、自然杀伤(NK)细胞和 B 细胞]、免疫球蛋白(Ig)(IgG、IgM 和 IgA)、C 反应蛋白(CRP)和全血细胞计数。在败血症组,第一个时间段的 IL6、TNF-α、IL1-b 和 CRP 较高,在第二个时间段,IL6 和 TNF-α 继续在该组中升高。IL-6 和 TNF-α 是精确的败血症预测因子,其敏感性和特异性分别为 0.92、0.98 和 0.91、0.92。在败血症和疑似感染组中,NK 细胞、B 细胞、CD3+、CD4+、CD8+较高,但 CD3+/CD4+、CD3+/CD8+、CD4+/CD8+的比值与对照组无差异。败血症组 IgG 较低,IgM 较高。在对照组中,CD3+、CD4+、CD8+淋巴细胞随年龄增长而增加。结论:IL-6 和 TNF 是足月新生儿败血症的良好诊断标志物。淋巴细胞亚群受临床状况和时间顺序年龄的影响。NK 和 B 细胞可能在疑似和确诊败血症中升高,需要进一步研究以确定其临床意义。

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