Proinflammatory Cytokine Profiles in Both Mild Symptomatic and Asymptomatic SARS-CoV-2-Infected Egyptian Individuals and a Proposed Relationship to Post-COVID-19 Sequela.

IF 1.5 4区 医学 Q4 IMMUNOLOGY
Viral immunology Pub Date : 2023-11-01 Epub Date: 2023-10-13 DOI:10.1089/vim.2023.0060
Mahmoud M Bahgat, Rola Nadeem, Mohamed H Nasraa, Khaled Amer, Wael A Hassan, Fadya M ELGarhy, Salem Reda, Dina N Abd-Elshafy
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引用次数: 0

Abstract

Severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2) infection is associated with proinflammatory cytokine release as mediators of host antiviral response to the infection. Cytokine persistent elevation leads to post-Coronavirus disease-2019 (COVID-19) post-COVID-19 sequela (PCS) reported in about 60% of patients affecting individual's normal life after recovery. This study evaluates relationship of cytokines and chemokines pattern during and postinfection to PCS events. Serum samples collected from 82 individuals with symptomatic, asymptomatic, or no SARS-CoV-2 infection were classified as recently or formerly infected groups according to levels of anti-2019nCoV Immunoglobulin G/Immunoglobulin M. Levels of interleukin (IL)-1α, IL-1β, IL-6, IL-8, interferon alpha (IFN-α), tumor necrosis factor alpha (TNF-α), granulocyte macrophage colony-stimulating factor (GM-CSF), and monocyte chemoattractant protein-1 were assessed via ELISA for each individual. All asymptomatic groups showed nonsignificant differences in cytokines' levels than control group. Significant elevation of IFN-α, TNF-α, and GM-CSF levels were observed in recent symptomatic, while IFN-α and TNF-α levels were significant in former symptomatic groups. We observed an association between fever with IL-1α and IFN-α levels, fatigue with TNF-α and GM-CSF, dyspnea with IFN-α, TNF-α, and GM-CSF, and chest-wheezing with GM-CSF. Individuals were surveyed 12 months postsampling for PCS events. Among 35 responders to survey, 8 (22.8%) reported PCS events, 6 of which were females. Upon studying PCS events, IL-8, IFN-α, TNF-α, and GM-CSF levels showed significant elevation in active infection, that was not seen in a resolved state of infection. Cytokines patterns suggest that either a persistent elevation in levels or damage caused during infection contributes to PCS. Although with the limited sample size, our study emphasizes the importance to conduct medical approaches targeting the associated cytokines to improve the PCS symptoms.

轻度症状和无症状SARS-CoV-2感染埃及个体的炎性细胞因子谱及其与COVID-19后后遗症的拟议关系。
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)感染与作为宿主对感染的抗病毒反应介质的促炎细胞因子释放有关。细胞因子持续升高导致2019年冠状病毒病(新冠肺炎)后新冠肺炎后遗症(PCS),约60%的患者在康复后影响个人的正常生活。本研究评估了感染期间和感染后细胞因子和趋化因子模式与PCS事件的关系。根据抗2019nCoV免疫球蛋白G/免疫球蛋白M的水平,从82名有症状、无症状或无严重急性呼吸系统综合征冠状病毒2型感染者收集的血清样本被分为近期或既往感染组。白细胞介素(IL)-1α、IL-1β、IL-6、IL-8、干扰素-α、肿瘤坏死因子-α,粒细胞-巨噬细胞集落刺激因子(GM-CSF)和单核细胞趋化蛋白-1通过ELISA对每个个体进行评估。与对照组相比,所有无症状组的细胞因子水平均无显著差异。在近期症状组中观察到IFN-α、TNF-α和GM-CSF水平显著升高,而在既往症状组中IFN-α和TNF-α水平显著升高。我们观察到发烧与IL-1α和IFN-α水平、疲劳与TNF-α和GM-CSF、呼吸困难与IFN-α、TNF-α、GM-CSF以及胸部喘息与GM-CSF之间存在关联。个体在PCS事件采样后12个月接受调查。在35名调查响应者中,8人(22.8%)报告了PCS事件,其中6人为女性。在研究PCS事件后,IL-8、IFN-α、TNF-α和GM-CSF水平在活动性感染中显示出显著升高,而在感染缓解状态下则没有发现。细胞因子模式表明,水平的持续升高或感染期间造成的损伤都会导致PCS。尽管样本量有限,但我们的研究强调了针对相关细胞因子进行医学治疗以改善PCS症状的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Viral immunology
Viral immunology 医学-病毒学
CiteScore
3.60
自引率
0.00%
发文量
84
审稿时长
6-12 weeks
期刊介绍: Viral Immunology delivers cutting-edge peer-reviewed research on rare, emerging, and under-studied viruses, with special focus on analyzing mutual relationships between external viruses and internal immunity. Original research, reviews, and commentaries on relevant viruses are presented in clinical, translational, and basic science articles for researchers in multiple disciplines. Viral Immunology coverage includes: Human and animal viral immunology Research and development of viral vaccines, including field trials Immunological characterization of viral components Virus-based immunological diseases, including autoimmune syndromes Pathogenic mechanisms Viral diagnostics Tumor and cancer immunology with virus as the primary factor Viral immunology methods.
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