脓毒症患者th2导向反应标志物与SOFA评分的相关性

L. P. Fabbri, V. Santarlasci, M. Nucera, F. Liotta, C. Becchi, L. Cosmi, M. A. Malyan, E. Maggi, S. Boncinelli, F. Annunziato
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引用次数: 1

摘要

从Th1-到th2型细胞免疫反应的转变被认为发生在败血症期间,导致细胞介导的免疫抑制和预后不良。目的是研究新旧Th2标志物与败血症临床转归的关系。30例48小时的脓毒症危重患者参加了一项前瞻性临床研究。在入组时、第5天和第10天采集血样。评估血清总IgE和与Th1-和Th2反应相关的可溶性趋化因子水平。流式细胞术检测CD4+、CD8+ t细胞和CRTH2+ t细胞亚群的百分比和绝对数量。用SOFA评分评估脓毒症严重程度。脓毒症患者总IgE均值显著高于对照组(p<0.01)。死亡患者的IgE水平高于存活患者(p<0.05)。不同时间点IgE水平与SOFA评分呈正相关,RANTES与SOFA评分呈负相关(p<0.01)。不同时间点CRTH2+/CD4+ T细胞百分比与SOFA有显著相关性(p<0.05),而CRTH2+/CD8+ T细胞百分比与SOFA无显著相关性。总IgE、循环CRTh2+CD4+T细胞百分比与临床结果之间的直接相关性表明,败血症的临床恶化与向主要的保护性较低的Th2表型转变密切相关。虽然这些都是初步的结果,在疾病期间这些参数的纵向分析可以作为脓毒症的有用预后工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correlation Between Markers of TH2-Oriented Response and SOFA Score in Sepsis
A shift from Th1- to Th2-type cell immune response has been suggested to occur during sepsis, contributing to cell-mediated immunity suppression and to poor prognosis. The aim was to study the relationship between old and new Th2 markers and the clinical outcome of sepsis. 30 critically ill patients with sepsis for � 48 hours were enrolled in a pro- spective clinical study. Blood samples were collected at the enrolment, at the 5 th and 10 th day. Serum levels of total IgE and soluble chemokines related to Th1- and Th2 responses were evaluated. The percentages and absolute number of CD4+ and CD8+Tcells as well as CRTH2+Tcell subsets were detected by flow cytometry. Sepsis severity was assessed with SOFA score. The mean values of total IgE in septic patients were significantly higher than in controls(p<0.01). Moreover, IgE levels of septic patients who died were higher than those of survived patients(p<0.05). It has been found that IgE levels directly and RANTES inversely correlated with SOFA score at different time points(p<0.01). A significant correlation between the percentages of CRTH2+/CD4+(but not CRTH2+/CD8+)T cells and SOFA at different time points was observed(p<0.05). The direct correlation between total IgE, the percentages of circulating CRTh2+CD4+T cells and the clinical outcome suggests that clinical worsening of sepsis is closely linked to the shift towards a predominant less protective Th2 phenotype. Although these are preliminary results, the longitudinal analysis of these parameters during the disease could be proposed as useful prognostic tools in sepsis.
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