不同年龄儿童感染新型冠状病毒 COVID-19 后急性期和长期病程的临床和免疫学特征比较

О. М. Olenkova, О. Р. Kovtun, Y. Beikin, А. S. Sokolova
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摘要

本研究的目的是确定 COVID-19 在儿童中的临床和免疫学特征,并评估感染后长期的免疫系统状态。材料和方法。该研究是一项观察性队列回顾研究,包括对 87 名确诊新感染冠状病毒(COVID-19)的儿童的检查结果。所有患者都接受了实验室检查,以评估发病时和发病后 152 ± 11.57 天的免疫系统状况。对照组由 8-14 岁(26 人)和 15-18 岁(33 人)的健康儿童组成,他们没有冠状病毒感染史,并通过血清学检测证实了这一点。结果。在患病儿童中,72.2%为男孩(P < 0.001)。COVID-19 的临床表现以出现中毒和呼吸综合征为特征。主要表现为发烧、无痰咳嗽、流鼻涕、疼痛和/或咽喉痛。35.2%的病例中,患儿有并发症。8-14 岁患者发病时,中性粒细胞数量减少(p < 0.001),吸收活性降低(p = 0.01),CD3+HLA-DR+水平升高(p < 0.001),血清 IgM 水平低(p < 0.001),检测到 SARS-CoV-2 特异性 IgM 的存在;循环免疫复合物含量高(p < 0.001)。在 15-18 岁的儿童中,检测到 CD3+HLA-DR+ (p < 0.001)、TNK 细胞(p < 0.05)含量增加,血清总 IgM 和 IgG 水平下降(p < 0.001)。在感染后的长期阶段,8-14 岁的患者在发病初期发现的变化依然存在,单核细胞数量也有所减少(p < 0.05),B 淋巴细胞水平有所上升(p < 0.05)。在 15-18 岁组中,白细胞的杀菌活性增加(p = 0.03),单核细胞的吸收活性增加(p < 0.01)。结论该病主要以中度形式发展。在新冠状病毒感染初期,体液成分缺乏,学龄前儿童先天性免疫因子缺乏。在长期阶段,免疫图谱参数的偏差持续存在。有可能在儿童中形成免疫缺陷的危险群体,这就需要采取额外的监测和康复措施。
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Comparative clinical and immunological characteristics of the course of the new coronavirus infection COVID-19 in children of different ages in acute and long-term periods after illness
The purpose of the study is to establish the clinical and immunological characteristics of COVID-19 in children and to assess the state of the immune system in the long-term period after the infection. Materials and methods. An observational cohort retrospective study was conducted, which included the results of an examination of 87 children with confirmed new coronavirus infection (COVID-19). All patients underwent laboratory examination to assess the state of the immune system at the onset of the disease and 152 ± 11.57 days after the onset of the disease. The control groups consisted of practically healthy children 8—14 (n = 26) and 15—18 years old (n = 33), who had no history of coronavirus infection, which was verified by serological tests. Results. Of the sick people, 72.2% were boys (p < 0.001). The clinical picture of COVID-19 was determined by the presence of intoxication and respiratory syndromes. The main signs were fever, unproductive cough, nasal discharge, pain and/or sore throat. In 35.2% of cases, children had concomitant pathology. At the onset of the disease in patients aged 8—14 years, a decrease in the number of neutrophils (p < 0.001) and their absorption activity (p = 0.01), an increased level of CD3+HLA-DR+ (p < 0.001), and a low level of serum IgM were detected (p < 0.001), were detected the presence of specific IgM to SARS-CoV-2; high content of Circulating immune complexes (p < 0.001). In children aged 15—18 years, an increase in the content of CD3+HLA-DR+ (p < 0.001), TNK-cells (p < 0.05), and a decreased level of total serum IgM and IgG (p < 0.001) were detected. In the long-term period after infection, in patients 8—14 years old, the changes identified at the onset of the disease persist, and there is also a decrease in the number of monocytes (p < 0.05) and an increase in the level of B-lymphocytes (p < 0.05). In the group of 15—18 years old, there was an increase in the bactericidal activity of leukocytes (p = 0.03) and the absorption activity of monocytes (p < 0.01). Conclusion. The disease proceeded mainly in a moderate form. At the initial stage of the new coronavirus infection, there was a deficiency of the humoral component, and in children of early school age, a deficiency of innate immune factors. In the long-term period, deviations in immunogram parameters persist. There is a possibility of the formation of risk groups among children for immune deficiency, which requires additional monitoring and rehabilitation measures.
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