Clinical and immunological characteristics of post-COVID syndrome

E. V. Zhdanova, E. V. Rubtsova, E. Kostolomova
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Abstract

Aim. To evaluate changes in clinical manifestations and the cytokine profile of blood serum in patients with postCOVID syndrome. Materials and methods. The study involved 46 patients (37 women and 9 men) with signs of post-COVID syndrome 1–12 months after COVID-19 infection. COVID-19 infection was laboratory-confirmed (patients were tested positive for SARS-Cov-2 RNA using polymerase chain reaction (PCR), or they were tested positive for SARS-Cov-2 immunoglobulin (Ig)G antibodies after the end of the acute phase and in asymptomatic infection). Along with mandatory tests included in the regular health checkup of medical staff, the levels of interleukin (IL)-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-17, tumor necrosis factor alpha (TNFα), interferon gamma (INFγ), and total IgE were determined in the blood serum of patients. Results. The results showed that the development of post-COVID syndrome did not depend on the age and gender of patients and the severity of the acute phase of infection. Patients were more likely to develop postCOVID syndrome in the absence of antiviral therapy or in case of its ineffectiveness. A high level and imbalance of pro- and anti-inflammatory cytokines without laboratory signs of inflammation underlie the development of clinical manifestations at early stages of post-COVID syndrome (up to 3 months). The clinical presentation was characterized by symptoms of asthenia and functional disorders in the nervous, cardiovascular, and respiratory systems and gastrointestinal tract. After 3 months, the content of most cytokines returned to normal levels, whereas only the concentration of IL-17 remained elevated. Allergic and autoallergic mechanisms of damage to the skin, respiratory organs, and joints, as well as progression of cardiovascular pathology determined the clinical symptoms of post-COVID syndrome for 3–12 months. Conclusion. The changes in the cytokine profile over 12 months reflect different damage mechanisms at different periods of the post-COVID syndrome, which determines the range of its clinical manifestations.
后 COVID 综合征的临床和免疫学特征
目的评估后 COVID 综合征患者的临床表现和血清细胞因子谱的变化。材料和方法研究涉及 46 名在感染 COVID-19 后 1-12 个月出现后 COVID 综合征症状的患者(37 名女性和 9 名男性)。COVID-19 感染需经实验室确诊(患者通过聚合酶链反应 (PCR) 检测出 SARS-Cov-2 RNA 阳性,或在急性期结束后和无症状感染时检测出 SARS-Cov-2 免疫球蛋白 (Ig)G 抗体阳性)。除了医务人员定期体检中的必检项目外,还测定了患者血清中白细胞介素(IL)-1β、IL-2、IL-4、IL-6、IL-8、IL-10、IL-17、肿瘤坏死因子α(TNFα)、γ干扰素(INFγ)和总 IgE 的水平。结果显示结果显示,后 COVID 综合征的发生与患者的年龄、性别和急性感染期的严重程度无关。在缺乏抗病毒治疗或抗病毒治疗无效的情况下,患者更容易出现后 COVID 综合征。促炎症细胞因子和抗炎症细胞因子水平高且不平衡,但无实验室炎症迹象,这是导致 COVID 后综合征早期(3 个月内)出现临床表现的原因。临床表现的特点是气喘症状以及神经、心血管、呼吸系统和胃肠道功能紊乱。3 个月后,大多数细胞因子的含量恢复到正常水平,只有 IL-17 的浓度仍然升高。皮肤、呼吸器官和关节的过敏性和自身过敏性损伤机制以及心血管病变的进展决定了后 COVID 综合征的临床症状持续 3-12 个月。结论细胞因子谱在 12 个月内的变化反映了后 COVID 综合征不同时期的不同损伤机制,这决定了其临床表现的范围。
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