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本文引用的文献

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Congenital and opportunistic infections: Ureaplasma species and Mycoplasma hominis.先天性感染和机会性感染:脲原体属和人型支原体。
Semin Fetal Neonatal Med. 2009 Aug;14(4):190-9. doi: 10.1016/j.siny.2008.11.009. Epub 2008 Dec 23.
2
Induction, function and regulation of IL-17-producing T cells.产生白细胞介素-17的T细胞的诱导、功能及调控
Eur J Immunol. 2008 Oct;38(10):2636-49. doi: 10.1002/eji.200838535.
3
Impairment of T helper and T regulatory cell responses at birth.出生时辅助性T细胞和调节性T细胞反应受损。
Allergy. 2008 Nov;63(11):1438-47. doi: 10.1111/j.1398-9995.2008.01685.x.
4
Effects of blood sample handling procedures on measurable inflammatory markers in plasma, serum and dried blood spot samples.血样处理程序对血浆、血清和干血斑样本中可测量炎症标志物的影响。
J Immunol Methods. 2008 Jul 20;336(1):78-84. doi: 10.1016/j.jim.2008.04.006. Epub 2008 May 1.
5
Interleukin-6 (-174C) polymorphism and the risk of sepsis in very low birth weight infants: meta-analysis.白细胞介素-6(-174C)基因多态性与极低出生体重儿败血症风险:荟萃分析
Arch Dis Child Fetal Neonatal Ed. 2008 Nov;93(6):F427-9. doi: 10.1136/adc.2007.134205. Epub 2008 Mar 28.
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The fetal inflammatory response syndrome.胎儿炎症反应综合征
Clin Obstet Gynecol. 2007 Sep;50(3):652-83. doi: 10.1097/GRF.0b013e31811ebef6.
7
IL-17 family cytokines and the expanding diversity of effector T cell lineages.白细胞介素-17家族细胞因子与效应T细胞谱系不断扩大的多样性。
Annu Rev Immunol. 2007;25:821-52. doi: 10.1146/annurev.immunol.25.022106.141557.
8
Seventy-five years of neonatal sepsis at Yale: 1928-2003.耶鲁大学75年的新生儿败血症研究:1928 - 2003年
Pediatrics. 2005 Sep;116(3):595-602. doi: 10.1542/peds.2005-0552.
9
Simultaneous measurement of 25 inflammatory markers and neurotrophins in neonatal dried blood spots by immunoassay with xMAP technology.采用xMAP技术通过免疫测定法同时检测新生儿干血斑中的25种炎症标志物和神经营养因子。
Clin Chem. 2005 Oct;51(10):1854-66. doi: 10.1373/clinchem.2005.052241. Epub 2005 Aug 4.
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Neonatal adaptive immunity comes of age.新生儿适应性免疫已然成熟。
Nat Rev Immunol. 2004 Jul;4(7):553-64. doi: 10.1038/nri1394.

T 细胞细胞因子与极低出生体重儿血流感染的风险。

T cell cytokines and the risk of blood stream infection in extremely low birth weight infants.

机构信息

Department of Pediatrics, University of Alabama at Birmingham, Birmingham, AL, USA.

出版信息

Cytokine. 2011 Feb;53(2):249-55. doi: 10.1016/j.cyto.2010.11.003. Epub 2010 Dec 9.

DOI:10.1016/j.cyto.2010.11.003
PMID:21145756
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3042892/
Abstract

Cytokines mediate the host immune response to infectious micro-organisms. The objective of this study was to determine whether immune regulatory interleukins (IL-4, IL-5, IL-6, and IL-10) and inflammatory cytokines (Interferon-γ [INF-γ], tumor necrosis factor-β [TNF-β], IL-2, and IL-17) are associated with an increased risk of developing blood stream bacterial/fungal infection (BSI) in extremely low birth weight (ELBW) infants. ELBW infants from 17 NICHD Neonatal Research Network centers without early onset sepsis were studied. Cytokines were measured from blood on days 1, 3, 7, 14, and 21 after birth. 996 ELBW infants contributed a minimum of 4080 unique measurements for each cytokine during the five sampling periods. Infants with BSI had lower levels of the inflammatory cytokines IL-17 (p=0.01), and higher levels of the regulatory cytokines, IL-6 (p=0.01) and IL-10 (p<0.001). Higher levels of regulatory cytokines relative to pro-inflammatory cytokines were associated with increased risk of BSI even after adjusting for confounding variables. In ELBW infants, the ratio of immune regulatory cytokines to inflammatory cytokines was associated with development of BSI. Altered maturation of regulatory and inflammatory cytokines may increase the risk of serious infection in this population.

摘要

细胞因子介导宿主对感染微生物的免疫反应。本研究的目的是确定免疫调节白细胞介素(IL-4、IL-5、IL-6 和 IL-10)和炎症细胞因子(干扰素-γ[INF-γ]、肿瘤坏死因子-β[TNF-β]、IL-2 和 IL-17)是否与极低出生体重(ELBW)婴儿发生血流细菌/真菌感染(BSI)的风险增加有关。本研究纳入了来自 17 个 NICHD 新生儿研究网络中心且无早发性败血症的 ELBW 婴儿。在出生后第 1、3、7、14 和 21 天,从血液中测量细胞因子。996 名 ELBW 婴儿在五个采样期间至少提供了 4080 个独特的细胞因子测量值。BSI 婴儿的炎症细胞因子 IL-17 水平较低(p=0.01),而调节细胞因子 IL-6(p=0.01)和 IL-10(p<0.001)水平较高。即使在调整混杂变量后,调节性细胞因子相对于促炎细胞因子的较高水平与 BSI 的风险增加相关。在 ELBW 婴儿中,免疫调节细胞因子与炎症细胞因子的比值与 BSI 的发生有关。调节和炎症细胞因子成熟的改变可能会增加该人群严重感染的风险。