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Synergism of TNF-α and IFN-γ Triggers Inflammatory Cell Death, Tissue Damage, and Mortality in SARS-CoV-2 Infection and Cytokine Shock Syndromes.TNF-α 和 IFN-γ 的协同作用可引发 SARS-CoV-2 感染和细胞因子休克综合征中的炎症细胞死亡、组织损伤和死亡。
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Emerging Neurological and Psychobiological Aspects of COVID-19 Infection.新型冠状病毒肺炎感染的神经学和心理生物学新进展
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Inflammatory Cytokine: IL-17A Signaling Pathway in Patients Present with COVID-19 and Current Treatment Strategy.炎症细胞因子:COVID-19患者的IL-17A信号通路及当前治疗策略
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Cytokine profile and disease severity in patients with COVID-19.COVID-19 患者的细胞因子谱与疾病严重程度。
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IFN-γ is an independent risk factor associated with mortality in patients with moderate and severe COVID-19 infection.IFN-γ 是与中重度 COVID-19 感染患者死亡相关的独立危险因素。
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Transcriptomic analysis of COVID‑19 lungs and bronchoalveolar lavage fluid samples reveals predominant B cell activation responses to infection.新冠病毒感染患者肺及支气管肺泡灌洗液样本的转录组分析显示,感染后主要表现为 B 细胞激活反应。
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Considerations for target oxygen saturation in COVID-19 patients: are we under-shooting?新冠病毒患者目标血氧饱和度的考虑因素:我们是否设定得过低?
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The role of cytokine profile and lymphocyte subsets in the severity of coronavirus disease 2019 (COVID-19): A systematic review and meta-analysis.细胞因子谱和淋巴细胞亚群在 2019 年冠状病毒病(COVID-19)严重程度中的作用:系统评价和荟萃分析。
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辅助性 T 细胞 17 和辅助性 T 细胞 1 频率降低及其与严重 2019 冠状病毒病的关联。

Reduced frequency of T helper 17 and T helper 1 cells and their association with critical coronavirus disease 2019.

机构信息

Immunoregulation Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

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

出版信息

APMIS. 2021 May;129(5):271-279. doi: 10.1111/apm.13129. Epub 2021 Mar 31.

DOI:10.1111/apm.13129
PMID:33792109
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8250891/
Abstract

There is very little knowledge about the immune responses, particularly cellular immunity to coronavirus disease 2019 (COVID-19). The main objective of this study was to evaluate the frequency of T helper (Th) cell subtypes, including Th1, Th17, and Treg cells, in moderate-to-severe and critical COVID-19 patients compared to healthy controls. Twenty-nine moderate-to-severe and 13 critical patients confirmed for COVID-19, and 15 healthy subjects were included in this study. Interferon-γ (IFN-γ)-producing Th1 and interleukin-17A-producing Th17 and Treg cells in peripheral blood were measured with flow cytometry. The frequency of Th1 and Th17 was significantly decreased in critical patients compared to healthy subjects (aMD: -2.76 and - 2.34) and moderate-to-severe patients (aMD: -1.89 and - 1.89), respectively (p < 0.05). Differences were not significant between moderate-to-severe patients and healthy subjects for both Th1 (p = 0.358) and Th17 (p = 0.535), respectively. In contrast, significant difference was not observed between study subjects regarding the frequency of Treg cells. Patients with critical COVID-19 had a markedly lower Th1/Treg and Th17/Treg ratios compared with the controls and moderate-to-severe cases. Our study showed a dysregulated balance of Th1 and Th17 cells and its relation to the severity of COVID-19.

摘要

关于 2019 冠状病毒病(COVID-19)的免疫反应,特别是细胞免疫,人们知之甚少。本研究的主要目的是评估中度至重度和危重新冠肺炎患者与健康对照组相比,辅助性 T 细胞(Th)亚型,包括 Th1、Th17 和 Treg 细胞的频率。本研究纳入了 29 例中度至重度和 13 例危重新冠肺炎确诊患者,以及 15 名健康受试者。采用流式细胞术检测外周血中产生干扰素-γ(IFN-γ)的 Th1 和产生白细胞介素-17A 的 Th17 和 Treg 细胞。与健康对照组(aMD:-2.76 和-2.34)和中度至重度患者(aMD:-1.89 和-1.89)相比,危重症患者的 Th1 和 Th17 频率明显降低(p<0.05)。中度至重度患者与健康对照组的 Th1(p=0.358)和 Th17(p=0.535)之间的差异均无统计学意义。相比之下,研究对象之间 Treg 细胞的频率没有差异。危重新冠肺炎患者的 Th1/Treg 和 Th17/Treg 比值明显低于对照组和中度至重度病例。我们的研究显示,Th1 和 Th17 细胞的平衡失调与 COVID-19 的严重程度有关。