• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

I 型干扰素介导的中性粒细胞抗病毒能力的调节。

Type I Interferon-Mediated Regulation of Antiviral Capabilities of Neutrophils.

机构信息

Department of Pathobiology, Ontario Veterinary College, University of Guelph, Guelph, ON N1G2W1, Canada.

出版信息

Int J Mol Sci. 2021 Apr 29;22(9):4726. doi: 10.3390/ijms22094726.

DOI:10.3390/ijms22094726
PMID:33946935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8125486/
Abstract

Interferons (IFNs) are induced by viruses and are the main regulators of the host antiviral response. They balance tissue tolerance and immune resistance against viral challenges. Like all cells in the human body, neutrophils possess the receptors for IFNs and contribute to antiviral host defense. To combat viruses, neutrophils utilize various mechanisms, such as viral sensing, neutrophil extracellular trap formation, and antigen presentation. These mechanisms have also been linked to tissue damage during viral infection and inflammation. In this review, we presented evidence that a complex cross-regulatory talk between IFNs and neutrophils initiates appropriate antiviral immune responses and regulates them to minimize tissue damage. We also explored recent exciting research elucidating the interactions between IFNs, neutrophils, and severe acute respiratory syndrome-coronavirus-2, as an example of neutrophil and IFN cross-regulatory talk. Dissecting the IFN-neutrophil paradigm is needed for well-balanced antiviral therapeutics and development of novel treatments against many major epidemic or pandemic viral infections, including the ongoing pandemic of the coronavirus disease that emerged in 2019.

摘要

干扰素(IFNs)是由病毒诱导产生的,是宿主抗病毒反应的主要调节剂。它们平衡组织耐受和对病毒挑战的免疫抵抗。与人体所有细胞一样,中性粒细胞具有 IFN 受体,并有助于抗病毒宿主防御。为了对抗病毒,中性粒细胞利用多种机制,如病毒感应、中性粒细胞胞外陷阱形成和抗原呈递。这些机制也与病毒感染和炎症期间的组织损伤有关。在这篇综述中,我们提出了证据表明,IFNs 和中性粒细胞之间复杂的交叉调节对话启动了适当的抗病毒免疫反应,并对其进行调节以最大程度地减少组织损伤。我们还探讨了最近令人兴奋的研究,阐明了 IFN、中性粒细胞和严重急性呼吸系统综合征冠状病毒 2 之间的相互作用,这是中性粒细胞和 IFN 交叉调节对话的一个例子。为了平衡抗病毒治疗和开发针对许多主要传染病或大流行病毒感染的新疗法,包括 2019 年出现的持续大流行的冠状病毒病,需要剖析 IFN-中性粒细胞范式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2a4/8125486/359daf56735e/ijms-22-04726-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2a4/8125486/82588788a8ac/ijms-22-04726-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2a4/8125486/c8250976b561/ijms-22-04726-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2a4/8125486/359daf56735e/ijms-22-04726-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2a4/8125486/82588788a8ac/ijms-22-04726-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2a4/8125486/c8250976b561/ijms-22-04726-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2a4/8125486/359daf56735e/ijms-22-04726-g003.jpg

相似文献

1
Type I Interferon-Mediated Regulation of Antiviral Capabilities of Neutrophils.I 型干扰素介导的中性粒细胞抗病毒能力的调节。
Int J Mol Sci. 2021 Apr 29;22(9):4726. doi: 10.3390/ijms22094726.
2
Antiviral Activity of Type I, II, and III Interferons Counterbalances ACE2 Inducibility and Restricts SARS-CoV-2.I型、II型和III型干扰素的抗病毒活性可抵消ACE2的诱导性并限制新型冠状病毒。
mBio. 2020 Sep 10;11(5):e01928-20. doi: 10.1128/mBio.01928-20.
3
Type I and III interferon responses in SARS-CoV-2 infection.SARS-CoV-2 感染中的 I 型和 III 型干扰素反应。
Exp Mol Med. 2021 May;53(5):750-760. doi: 10.1038/s12276-021-00592-0. Epub 2021 May 6.
4
Virus Caused Imbalance of Type I IFN Responses and Inflammation in COVID-19.病毒导致 COVID-19 中 I 型干扰素反应和炎症失衡。
Front Immunol. 2021 Apr 12;12:633769. doi: 10.3389/fimmu.2021.633769. eCollection 2021.
5
Type I IFNs: A Blessing in Disguise or Partner in Crime in MERS-CoV-, SARS-CoV-, and SARS-CoV-2-Induced Pathology and Potential Use of Type I IFNs in Synergism with IFN- as a Novel Antiviral Approach Against COVID-19.I 型干扰素:在中东呼吸综合征冠状病毒、严重急性呼吸综合征冠状病毒和严重急性呼吸综合征冠状病毒 2 诱导的病理中的伪装祝福或共犯,以及 I 型干扰素与 IFN-协同作用作为针对 COVID-19 的新型抗病毒方法的潜在用途。
Viral Immunol. 2021 Jun;34(5):321-329. doi: 10.1089/vim.2020.0085. Epub 2020 Nov 11.
6
The unique regulation and functions of type III interferons in antiviral immunity.III型干扰素在抗病毒免疫中的独特调控与功能。
Curr Opin Virol. 2015 Jun;12:47-52. doi: 10.1016/j.coviro.2015.02.003. Epub 2015 Mar 12.
7
Detrimental Effect of Type I IFNs During Acute Lung Infection With Is Mediated Through the Stimulation of Neutrophil NETosis.Ⅰ型干扰素在急性肺感染中的有害作用是通过刺激中性粒细胞 NETosis 介导的。
Front Immunol. 2019 Sep 11;10:2190. doi: 10.3389/fimmu.2019.02190. eCollection 2019.
8
Untuned antiviral immunity in COVID-19 revealed by temporal type I/III interferon patterns and flu comparison.通过I/III型干扰素的时间模式及流感对比揭示的新冠病毒感染中失调的抗病毒免疫
Nat Immunol. 2021 Jan;22(1):32-40. doi: 10.1038/s41590-020-00840-x. Epub 2020 Dec 4.
9
An Update on Innate Immune Responses during SARS-CoV-2 Infection.关于 SARS-CoV-2 感染期间固有免疫反应的最新研究进展。
Viruses. 2021 Oct 14;13(10):2060. doi: 10.3390/v13102060.
10
Type I and Type III Interferons Restrict SARS-CoV-2 Infection of Human Airway Epithelial Cultures.Ⅰ型和Ⅲ型干扰素限制 SARS-CoV-2 感染人呼吸道上皮细胞。
J Virol. 2020 Sep 15;94(19). doi: 10.1128/JVI.00985-20.

引用本文的文献

1
The immune response against cancer is modulated by stromal cell fibronectin.针对癌症的免疫反应受基质细胞纤连蛋白的调节。
Neoplasia. 2025 Jun 30;67:101196. doi: 10.1016/j.neo.2025.101196.
2
Juruaça virus taxonomy, tolerance and resistance to infection, and inflammatory response modulation in murine model.茹鲁阿察病毒分类学、对感染的耐受性和抗性以及小鼠模型中的炎症反应调节
Npj Viruses. 2024 Oct 3;2(1):46. doi: 10.1038/s44298-024-00056-y.
3
Role of Neutrophils in Anti-Tumor Activity: Characteristics and Mechanisms of Action.中性粒细胞在抗肿瘤活性中的作用:特征与作用机制

本文引用的文献

1
IFN signaling and neutrophil degranulation transcriptional signatures are induced during SARS-CoV-2 infection.IFN 信号和嗜中性粒细胞脱粒的转录特征在 SARS-CoV-2 感染过程中被诱导。
Commun Biol. 2021 Mar 5;4(1):290. doi: 10.1038/s42003-021-01829-4.
2
Cutting Edge: NOX2 NADPH Oxidase Controls Infection by an Intracellular Bacterial Pathogen through Limiting the Type 1 IFN Response.前沿:NOX2 NADPH 氧化酶通过限制 I 型 IFN 反应来控制胞内细菌病原体的感染。
J Immunol. 2021 Jan 15;206(2):323-328. doi: 10.4049/jimmunol.2000694. Epub 2020 Dec 7.
3
Transcriptome of airway neutrophils reveals an interferon response in life-threatening respiratory syncytial virus infection.
Cancers (Basel). 2025 Apr 11;17(8):1298. doi: 10.3390/cancers17081298.
4
NLRC3 Attenuates Antiviral Innate Immune Response by Targeting IRF7 in Grass Carp ().NLRC3通过靶向草鱼中的IRF7减弱抗病毒天然免疫反应()。
Int J Mol Sci. 2025 Jan 20;26(2):840. doi: 10.3390/ijms26020840.
5
Neutrophil diversity and function in health and disease.中性粒细胞在健康与疾病中的多样性及功能。
Signal Transduct Target Ther. 2024 Dec 6;9(1):343. doi: 10.1038/s41392-024-02049-y.
6
Influence of Donor-Specific Characteristics on Cytokine Responses in H3N2 Influenza A Virus Infection: New Insights from an Ex Vivo Model.供体特异性特征对 H3N2 流感病毒感染中细胞因子反应的影响:来自体外模型的新见解。
Int J Mol Sci. 2024 Oct 11;25(20):10941. doi: 10.3390/ijms252010941.
7
MAP2K1 dampens cigarette smoke-induced inflammation via suppression of type I interferon pathway activation.MAP2K1 通过抑制 I 型干扰素通路的激活来抑制香烟烟雾诱导的炎症。
Am J Physiol Lung Cell Mol Physiol. 2024 Nov 1;327(5):L740-L748. doi: 10.1152/ajplung.00080.2024. Epub 2024 Sep 24.
8
Role of interferons in the antiviral battle: from virus-host crosstalk to prophylactic and therapeutic potential in SARS-CoV-2 infection.干扰素在抗病毒斗争中的作用:从病毒-宿主相互作用到 SARS-CoV-2 感染的预防和治疗潜力。
Front Immunol. 2024 Jan 15;14:1273604. doi: 10.3389/fimmu.2023.1273604. eCollection 2023.
9
Neutrophils in COVID-19: recent insights and advances.新型冠状病毒肺炎中的中性粒细胞:最新的认识和进展。
Virol J. 2023 Aug 2;20(1):169. doi: 10.1186/s12985-023-02116-w.
10
Baicalin promotes antiviral IFNs production and alleviates type I IFN-induced neutrophil inflammation.黄芩苷促进抗病毒 IFN 的产生并减轻 I 型 IFN 诱导的中性粒细胞炎症。
J Nat Med. 2023 Sep;77(4):677-687. doi: 10.1007/s11418-023-01702-0. Epub 2023 Jul 25.
气道中性粒细胞转录组揭示了危及生命的呼吸道合胞病毒感染中的干扰素反应。
Clin Immunol. 2020 Nov;220:108593. doi: 10.1016/j.clim.2020.108593. Epub 2020 Sep 11.
4
Characterization of the Impact of Oncolytic Vesicular Stomatitis Virus on the Trafficking, Phenotype, and Antigen Presentation Potential of Neutrophils and Their Ability to Acquire a Non-Structural Viral Protein.溶瘤性单纯疱疹病毒对中性粒细胞的迁移、表型和抗原呈递能力及其获取非结构病毒蛋白能力的影响特征。
Int J Mol Sci. 2020 Sep 1;21(17):6347. doi: 10.3390/ijms21176347.
5
Neutrophil Extracellular Traps (NETs) and Damage-Associated Molecular Patterns (DAMPs): Two Potential Targets for COVID-19 Treatment.中性粒细胞胞外诱捕网(NETs)和损伤相关分子模式(DAMPs):COVID-19 治疗的两个潜在靶点。
Mediators Inflamm. 2020 Jul 16;2020:7527953. doi: 10.1155/2020/7527953. eCollection 2020.
6
COVID-19 Hyperinflammation: What about Neutrophils?COVID-19 超高炎症反应:中性粒细胞怎么了?
mSphere. 2020 Jun 24;5(3):e00367-20. doi: 10.1128/mSphere.00367-20.
7
Pathological inflammation in patients with COVID-19: a key role for monocytes and macrophages.COVID-19 患者的病理性炎症:单核细胞和巨噬细胞的关键作用。
Nat Rev Immunol. 2020 Jun;20(6):355-362. doi: 10.1038/s41577-020-0331-4. Epub 2020 May 6.
8
Differential expression of interferon-lambda receptor 1 splice variants determines the magnitude of the antiviral response induced by interferon-lambda 3 in human immune cells.干扰素-λ受体 1 剪接变异体的差异表达决定了干扰素-λ 3 在人免疫细胞中诱导的抗病毒反应的幅度。
PLoS Pathog. 2020 Apr 30;16(4):e1008515. doi: 10.1371/journal.ppat.1008515. eCollection 2020 Apr.
9
Targeting potential drivers of COVID-19: Neutrophil extracellular traps.靶向 COVID-19 的潜在驱动因素:中性粒细胞胞外陷阱。
J Exp Med. 2020 Jun 1;217(6). doi: 10.1084/jem.20200652.
10
COVID-19, SARS and MERS: are they closely related?新型冠状病毒肺炎、严重急性呼吸综合征和中东呼吸综合征:它们有何关联?
Clin Microbiol Infect. 2020 Jun;26(6):729-734. doi: 10.1016/j.cmi.2020.03.026. Epub 2020 Mar 28.