慢性巨细胞病毒感染婴儿在缺氧缺血性中枢神经系统损伤背景下检测细胞因子状态的临床和诊断意义

L. Kravchenko, M. Levkovich, S. Berezhanskaya, A. Afonin, I. Krukier, O. Puzikova, I. Panova, D. Sozaeva, V. Popova, N. Drukker
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引用次数: 0

摘要

目的:基于细胞因子的产生,探讨在缺氧缺血性中枢神经系统损伤背景下一岁儿童巨细胞病毒感染慢性病程的免疫学特征。研究方法:对108例以围生期中央不等系统缺氧缺血性病变为背景发生巨细胞病毒感染的新生儿进行检查。所有观察到的巨细胞病毒感染患者在诊断后立即进行免疫学检查,包括测定干扰素-α (IFN-α)和干扰素-γ (IFN-γ)水平,采用酶免疫分析法测定血清中白细胞介素-2和4 (IL -2和IL-4)坏死因子人α肿瘤(TNF-α)的水平,使用一套试剂ProCon IF2 plus, ProCon Ifgamma, ProCon TNFα (Protein contour LLC,俄罗斯,圣彼得堡)。1、6月龄时,观察组为急性病程患儿78例(72.2%),慢性病程患儿30例(27.3%),对照组为未感染疱疹病毒的新生儿15例。在所研究的细胞因子中,发现IL-2、IFN-γ对1岁儿童巨细胞病毒感染的慢性病程具有统计学意义,背景是缺氧缺血性中枢神经系统损伤。研究发现,6月龄时血清中IFN-γ持续低水平和IL-4水平升高的儿童,在围产期缺氧缺血性中枢神经系统损伤的背景下,存在巨细胞病毒感染的慢性病程。IFN-γ产生减少表明先天性或获得性干扰素系统缺陷,可视为长期干扰素替代治疗的指征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical and diagnostic significance of determining the cytokine status in infants with chronic cytomegalovirus infection against the background of hypoxic-ischemic CNS damage
Objective: based on the production of cytokines, to identify the immunological features of the chronic course of cytomegalovirus infection in children of the first year of life against the background of hypoxic-ischemic CNS damage.Research methods:108 newborns with cytomegalovirus infection occurring against the background of perinatal hypoxic-ischemic lesions of the central unequal system were examined. All observed patients immediately after the diagnosis of cytomegalovirus infection underwent an immunological examination, including the determination of the levels of interferon-alpha (IFN-α) and interferon-gamma (IFN-γ), the level of interleukins — 2 and 4 (IL -2 and IL-4) necrosis factor human alpha tumors (TNF-α in blood serum was determined by enzyme immunoassay using a set of reagents ProCon IF2 plus, ProCon Ifgamma, ProCon TNFα (Protein contour LLC, Russia, St. Petersburg). At 1 and 6 months of life .The observation groups consisted of 78 children (72.2%) with an acute course of the disease (Group 1) and 30 children (27.3%) with a chronic course (Group 2). The control group consisted of 15 newborns without herpes virus infection.Results. Of the totality of the studied cytokines, statistically significant for the chronic course of cytomegalovirus infection in children of the first year of life against the background of hypoxic-ischemic CNS damage were found: IL-2, IFN-γ. It was found that in children with a persistent low level of IFN-γ and an increased level of IL-4 in the blood serum at the age of 6 months, there was a chronic course of cytomegalovirus infection against the background of perinatal hypoxic-ischemic CNS damage.A decrease in IFN-γ production indicates a congenital or acquired deficiency of the interferon system and can be considered as an indication for long-term interferon replacement therapy.
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