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本文引用的文献

1
Neutrophils as Suppressors of T Cell Proliferation: Does Age Matter?中性粒细胞对 T 细胞增殖的抑制作用:年龄是否重要?
Front Immunol. 2019 Sep 11;10:2144. doi: 10.3389/fimmu.2019.02144. eCollection 2019.
2
Tumour-associated neutrophils in patients with cancer.癌症患者肿瘤相关中性粒细胞。
Nat Rev Clin Oncol. 2019 Oct;16(10):601-620. doi: 10.1038/s41571-019-0222-4.
3
Fatty acid transport protein 2 reprograms neutrophils in cancer.脂肪酸转运蛋白 2 重编程癌症中的中性粒细胞。
Nature. 2019 May;569(7754):73-78. doi: 10.1038/s41586-019-1118-2. Epub 2019 Apr 17.
4
CARD9 microglia promote antifungal immunity via IL-1β- and CXCL1-mediated neutrophil recruitment.CARD9 小胶质细胞通过 IL-1β 和 CXCL1 介导的中性粒细胞募集来促进抗真菌免疫。
Nat Immunol. 2019 May;20(5):559-570. doi: 10.1038/s41590-019-0377-2. Epub 2019 Apr 17.
5
Mature neutrophils suppress T cell immunity in ovarian cancer microenvironment.成熟中性粒细胞在卵巢癌微环境中抑制 T 细胞免疫。
JCI Insight. 2019 Mar 7;4(5). doi: 10.1172/jci.insight.122311.
6
Neutrophils escort circulating tumour cells to enable cell cycle progression.中性粒细胞护送循环肿瘤细胞以促进细胞周期进程。
Nature. 2019 Feb;566(7745):553-557. doi: 10.1038/s41586-019-0915-y. Epub 2019 Feb 6.
7
Plerixafor for the Treatment of WHIM Syndrome.普乐沙福治疗 WHIM 综合征。
N Engl J Med. 2019 Jan 10;380(2):163-170. doi: 10.1056/NEJMoa1808575.
8
Neutrophils facilitate ovarian cancer premetastatic niche formation in the omentum.中性粒细胞促进卵巢癌细胞在大网膜中形成转移前生态位。
J Exp Med. 2019 Jan 7;216(1):176-194. doi: 10.1084/jem.20181170. Epub 2018 Dec 19.
9
Neutrophil extracellular traps produced during inflammation awaken dormant cancer cells in mice.中性粒细胞胞外诱捕网在炎症期间产生,可唤醒小鼠体内休眠的癌细胞。
Science. 2018 Sep 28;361(6409). doi: 10.1126/science.aao4227.
10
Human CARD9: A Critical Molecule of Fungal Immune Surveillance.人类 CARD9:真菌免疫监视的关键分子。
Front Immunol. 2018 Aug 6;9:1836. doi: 10.3389/fimmu.2018.01836. eCollection 2018.

中性粒细胞在宿主防御和疾病中的作用。

The role of neutrophils in host defense and disease.

机构信息

Division of Allergy/Immunology & Rheumatology, Department of Pediatrics, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY.

Roswell Park Comprehensive Cancer Center, University at Buffalo, Buffalo, NY.

出版信息

J Allergy Clin Immunol. 2020 Jun;145(6):1535-1544. doi: 10.1016/j.jaci.2020.02.038. Epub 2020 Apr 10.

DOI:10.1016/j.jaci.2020.02.038
PMID:32283205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8912989/
Abstract

Neutrophils, the most abundant circulating leukocyte, are critical for host defense. Granulopoiesis is under the control of transcriptional factors and culminates in mature neutrophils with a broad armamentarium of antimicrobial pathways. These pathways include nicotinamide adenine dinucleotide phosphate oxidase, which generates microbicidal reactive oxidants, and nonoxidant pathways that target microbes through several mechanisms. Activated neutrophils can cause or worsen tissue injury, underscoring the need for calibration of activation and resolution of inflammation when infection has been cleared. Acquired neutrophil disorders are typically caused by cytotoxic chemotherapy or immunosuppressive agents. Primary neutrophil disorders typically result from disabling mutations of individual genes that result in impaired neutrophil number or function, and provide insight into basic mechanisms of neutrophil biology. Neutrophils can also be activated by noninfectious causes, including trauma and cellular injury, and can have off-target effects in which pathways that typically defend against infection exacerbate injury and disease. These off-target effects include acute organ injury, autoimmunity, and variable effects on the tumor microenvironment that can limit or worsen tumor progression. A greater understanding of neutrophil plasticity in these conditions is likely to pave the way to new therapeutic approaches.

摘要

中性粒细胞是循环白细胞中最丰富的一种,对宿主防御至关重要。粒细胞生成受转录因子的控制,最终产生具有广泛抗菌途径的成熟中性粒细胞。这些途径包括烟酰胺腺嘌呤二核苷酸磷酸氧化酶,它产生杀菌活性氧,以及通过几种机制靶向微生物的非氧化途径。激活的中性粒细胞可导致或加重组织损伤,这突显了在感染清除后,需要对激活进行校准并解决炎症。获得性中性粒细胞疾病通常由细胞毒性化疗或免疫抑制药物引起。原发性中性粒细胞疾病通常是由于单个基因的失能突变导致中性粒细胞数量或功能受损引起的,这为中性粒细胞生物学的基本机制提供了深入了解。中性粒细胞也可以被非感染性原因激活,包括创伤和细胞损伤,并且在通常针对感染的防御途径加剧损伤和疾病的情况下会产生脱靶效应。这些脱靶效应包括急性器官损伤、自身免疫和对肿瘤微环境的可变影响,这些影响可能会限制或加重肿瘤进展。对这些情况下中性粒细胞可塑性的更多了解可能会为新的治疗方法铺平道路。

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