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新冠病毒感染恢复期的免疫系统变化在决定疾病严重程度方面起着关键作用。

Immune system changes during COVID-19 recovery play key role in determining disease severity.

机构信息

Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Internal Medicine, School of Medicine, Khorshid Hospital, Isfahan University of Medical Science, Isfahan, Iran.

出版信息

Int J Immunopathol Pharmacol. 2020 Jan-Dec;34:2058738420966497. doi: 10.1177/2058738420966497.

DOI:10.1177/2058738420966497
PMID:33076729
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7594220/
Abstract

Coronavirus disease 2019 (COVID-19), an acute respiratory infection, is largely associated with dysregulation and impairment of the immune system. This study investigated how the immune system changes were related to disease severity in COVID-19 patients. The frequencies of different immune cells and levels of pro- and anti-inflammatory cytokines in whole blood of participants were determined by flow cytometry and enzyme-linked immunosorbent assay, respectively. The values of other inflammatory agents were also studied. In the late recovery stage, unlike CD56 CD16 NK cells and monocytes, CD56 CD16 NK cell numbers were increased ( < 0.0001-0.05). Th1, Th2, and Th17 cell percentages were significantly lower in patients than healthy control ( < 0.0001-0.05), while their frequencies were increased following disease recovery ( < 0.0001-0.05). The numbers of Tregs, activated CD4+ T cells, and exhausted CD8+ T cells were significantly decreased during a recovery ( < 0.0001-0.05). No significant change was observed in exhausted CD4+ T cell number during a recovery ( > 0.05). B cell showed an increased percentage in patients compared to healthy subjects ( < 0.0001-0.05), whereas its number was reduced following recovery ( < 0.0001-0.05). IL-1α, IL-1β, IL-6, TNF-α, and IL-10 levels were significantly decreased in the late recovery stage ( < 0.0001-0.05). However, TGF-β1 level was not significantly changed during the recovery ( > 0.05). Lymphocyte numbers in patients were significantly decreased ( < 0.001), unlike ESR value ( < 0.001). Lymphocyte number was negatively correlated to ESR value and Th2 number ( < 0.05), while its association with monocyte was significantly positive at the first day of recovery ( < 0.05). The immune system changes during the disease recovery to improve and regulate immune responses and thereby may associate with the reduction in disease severity.

摘要

新型冠状病毒病(COVID-19)是一种急性呼吸道传染病,主要与免疫系统的失调和损伤有关。本研究旨在探讨 COVID-19 患者的免疫系统变化与疾病严重程度的关系。通过流式细胞术和酶联免疫吸附试验分别测定参与者全血中不同免疫细胞的频率和促炎及抗炎细胞因子的水平。还研究了其他炎症因子的水平。在疾病恢复的晚期,与 CD56 CD16 NK 细胞和单核细胞不同,CD56 CD16 NK 细胞数量增加( < 0.0001-0.05)。与健康对照组相比,患者的 Th1、Th2 和 Th17 细胞比例明显降低( < 0.0001-0.05),而在疾病恢复后频率增加( < 0.0001-0.05)。恢复过程中 Treg、活化 CD4+T 细胞和耗竭 CD8+T 细胞的数量显著减少( < 0.0001-0.05)。恢复过程中耗竭 CD4+T 细胞数量无明显变化( > 0.05)。与健康对照组相比,患者的 B 细胞百分比增加( < 0.0001-0.05),而恢复后数量减少( < 0.0001-0.05)。IL-1α、IL-1β、IL-6、TNF-α 和 IL-10 水平在疾病恢复的晚期显著降低( < 0.0001-0.05)。然而,TGF-β1 水平在恢复过程中没有明显变化( > 0.05)。与健康对照组相比,患者的淋巴细胞数量显著减少( < 0.001),而 ESR 值没有变化( < 0.001)。淋巴细胞数量与 ESR 值和 Th2 数量呈负相关( < 0.05),而与单核细胞的相关性在恢复的第一天显著为正( < 0.05)。疾病恢复过程中免疫系统的变化可改善和调节免疫反应,从而可能与疾病严重程度的降低有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b2/7594220/6508b823916e/10.1177_2058738420966497-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b2/7594220/9e6636e2c56f/10.1177_2058738420966497-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b2/7594220/09acc184925f/10.1177_2058738420966497-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b2/7594220/6508b823916e/10.1177_2058738420966497-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b2/7594220/9e6636e2c56f/10.1177_2058738420966497-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b2/7594220/09acc184925f/10.1177_2058738420966497-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51b2/7594220/6508b823916e/10.1177_2058738420966497-fig4.jpg

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