Kolesnik Ya, Zharkova T, Rzhevskaya O, Kvaratskheliya T, Sorokina O
Kharkiv National Medical University, Department of Children's Infectious Diseases; V.N. Karasin Kharkov National University, Department of Pediatrics №2; Department of Clinical Immunology and Allergy, Ukraine.
Georgian Med News. 2018 May(278):132-138.
The article presents the results of our own studies to determine the criteria for the adverse variants of the course of infectious mononucleosis (IM) in children. The study was conducted in the regional children's infectious clinical hospital in Kharkov. 161 children aged three to fifteen years were under observation with diagnosis of infectious moninucleosis. Out of 161 ill children, 140 (86.9%) had moderate severity of disease, and 21 (13.1%) had severe forms. All children were prescribed standard clinical and laboratory-instrumental examinations. The diagnosis of IM was verified by PCR (detection of VEB DNA in the blood) and ELISA (anti-VEB Ig M and Ig G). In 140 children (86.9%) IM proceeded sharply, smoothly (the first group), in 21 (13.1%) - unfavorably (wave and / or prolonged course) - the second group. The groups were comparable according to age, the severity of the disease and other parameters. All children received therapy according to approved protocols (Order of the Ministry of Health of Ukraine No. 354 of 09.07.2004). Immune status of children was assessed by determining the relative contents of CD3 +, CD4 +, CD8 +, CD16 +, CD19 + blood cells with appropriate monoclonal antibodies, serum IgA, IgM, IgG concentration by Mancini and interleukin (IL) -1β cytokine response and - 4, tumor necrosis factor (TNF α) is a solid-phase enzyme-linked immunosorbent assay. Based on the results of observations, it was established that the prognostically unfavorable criteria of IМ at the stages of manifestation of disease include: generalized lymphadenopathy involving 5-6 groups of lymph nodes and a significant increasing of them, purulent tonsillitis, marked increasing of size of liver and spleen on the background of anemia, thrombocytopenia, neutropenia and the absence of atypical mononuclears in the complete blood count. There is a depression of the cellular link and an increase in the humoral mechanisms of immune responses in case of development of adverse course of IM.
本文介绍了我们自己的研究结果,以确定儿童传染性单核细胞增多症(IM)病程不良变异的标准。该研究在哈尔科夫的地区儿童传染病临床医院进行。对161名3至15岁诊断为传染性单核细胞增多症的儿童进行了观察。在161名患病儿童中,140名(86.9%)疾病严重程度为中度,21名(13.1%)为重度。所有儿童均接受了标准的临床和实验室仪器检查。通过PCR(检测血液中的EBV DNA)和ELISA(抗EBV Ig M和Ig G)对IM诊断进行了验证。140名儿童(86.9%)的IM病程急剧、顺利(第一组),21名(13.1%)则病程不利(呈波浪状和/或病程延长)——第二组。两组在年龄、疾病严重程度和其他参数方面具有可比性。所有儿童均按照批准的方案(乌克兰卫生部2004年7月9日第354号命令)接受治疗。通过使用适当的单克隆抗体测定CD3 +、CD4 +、CD8 +、CD16 +、CD19 +血细胞的相对含量、通过曼奇尼法测定血清IgA、IgM、IgG浓度以及通过固相酶联免疫吸附测定白细胞介素(IL)-1β细胞因子反应和 - 4、肿瘤坏死因子(TNFα)来评估儿童的免疫状态。基于观察结果确定,IM在疾病表现阶段预后不良的标准包括:累及5 - 6组淋巴结的全身性淋巴结病且淋巴结明显增大、化脓性扁桃体炎、在贫血、血小板减少、中性粒细胞减少背景下肝脏和脾脏大小明显增加以及全血细胞计数中无异常单核细胞。在IM病程不利发展的情况下,细胞免疫环节会受到抑制,免疫反应的体液机制会增强。