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流感病毒感染后二次感染期促炎细胞因子的中和作用。

Neutralization of Pro-inflammatory Cytokines During Secondary Infection Post Influenza A Virus Infection.

机构信息

Frankfurt Institute for Advanced Studies, Frankfurt am Main, Germany.

Immune Regulation Group, Helmholtz Centre for Infection Research (HZI), Braunschweig, Germany.

出版信息

Front Immunol. 2019 Aug 14;10:1864. doi: 10.3389/fimmu.2019.01864. eCollection 2019.

DOI:10.3389/fimmu.2019.01864
PMID:31474978
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6702285/
Abstract

An overt pro-inflammatory immune response is a key factor contributing to lethal pneumococcal infection in an influenza pre-infected host and represents a potential target for therapeutic intervention. However, there is a paucity of knowledge about the level of contribution of individual cytokines. Based on the predictions of our previous mathematical modeling approach, the potential benefit of IFN-γ- and/or IL-6-specific antibody-mediated cytokine neutralization was explored in C57BL/6 mice infected with the influenza A/PR/8/34 strain, which were subsequently infected with the strain TIGR4 on day 7 post influenza. While single IL-6 neutralization had no effect on respiratory bacterial clearance, single IFN-γ neutralization enhanced local bacterial clearance in the lungs. Concomitant neutralization of IFN-γ and IL-6 significantly reduced the degree of pneumonia as well as bacteremia compared to the control group, indicating a positive effect for the host during secondary bacterial infection. The results of our model-driven experimental study reveal that the predicted therapeutic value of IFN-γ and IL-6 neutralization in secondary pneumococcal infection following influenza infection is tightly dependent on the experimental protocol while at the same time paving the way toward the development of effective immune therapies.

摘要

过度的促炎免疫反应是导致流感感染宿主发生致命性肺炎球菌感染的关键因素,代表了治疗干预的潜在靶点。然而,关于个别细胞因子的贡献程度,我们的了解还很匮乏。基于我们之前的数学建模方法的预测,在感染了流感 A/PR/8/34 株的 C57BL/6 小鼠中,探索了针对 IFN-γ 和/或 IL-6 的特异性抗体介导的细胞因子中和的潜在益处,随后在流感后第 7 天感染了 TIGR4 株。虽然单独中和 IL-6 对呼吸道细菌清除没有影响,但单独中和 IFN-γ 增强了肺部的局部细菌清除。与对照组相比,同时中和 IFN-γ 和 IL-6 显著降低了肺炎和菌血症的程度,表明在二次细菌感染期间对宿主有积极影响。我们的模型驱动实验研究的结果表明,在流感感染后继发肺炎球菌感染中,中和 IFN-γ 和 IL-6 的预测治疗价值与实验方案密切相关,同时为开发有效的免疫治疗方法铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e63/6702285/fdda28af9b75/fimmu-10-01864-g0008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e63/6702285/fdda28af9b75/fimmu-10-01864-g0008.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e63/6702285/9ebdec26eba5/fimmu-10-01864-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e63/6702285/0ff7b91dec23/fimmu-10-01864-g0005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9e63/6702285/fdda28af9b75/fimmu-10-01864-g0008.jpg

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本文引用的文献

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Nat Immunol. 2018 Dec;19(12):1299-1308. doi: 10.1038/s41590-018-0231-y. Epub 2018 Oct 29.
2
Neuraminidase Inhibitors in Influenza Treatment and Prevention⁻Is It Time to Call It a Day?神经氨酸酶抑制剂在流感治疗和预防中的作用——是时候说再见了吗?
Viruses. 2018 Aug 25;10(9):454. doi: 10.3390/v10090454.
3
Effects of Influenza on Alveolar Macrophage Viability Are Dependent on Mouse Genetic Strain.
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Microorganisms. 2023 Dec 13;11(12):2974. doi: 10.3390/microorganisms11122974.
4
Generation of "OP7 chimera" defective interfering influenza A particle preparations free of infectious virus that show antiviral efficacy in mice.生成无感染性病毒的“OP7 嵌合体”缺陷型干扰流感 A 粒子制剂,在小鼠中显示抗病毒功效。
Sci Rep. 2023 Nov 28;13(1):20936. doi: 10.1038/s41598-023-47547-1.
5
NLRP6 Induces Lung Injury and Inflammation Early in Brucella and Influenza Coinfection.NLRP6在布鲁氏菌和流感病毒合并感染早期诱发肺损伤和炎症。
J Pers Med. 2022 Dec 14;12(12):2063. doi: 10.3390/jpm12122063.
6
Predicting Influenza A Virus Infection in the Lung from Hematological Data with Machine Learning.用机器学习从血液学数据预测肺部甲型流感病毒感染。
mSystems. 2022 Dec 20;7(6):e0045922. doi: 10.1128/msystems.00459-22. Epub 2022 Nov 8.
7
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8
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Front Microbiol. 2017 Jun 23;8:1041. doi: 10.3389/fmicb.2017.01041. eCollection 2017.
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9
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Pulm Pharmacol Ther. 2017 Jun;44:96-105. doi: 10.1016/j.pupt.2017.03.008. Epub 2017 Mar 15.
10
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