减少中性粒细胞可减轻小鼠肺炎球菌肺炎早期肺损伤的严重程度

IF 3.6 2区 医学 Q1 PHYSIOLOGY
Hiroki Taenaka, Xiaohui Fang, Mazharul Maishan, Alpa Trivedi, Katherine D Wick, Jeffrey E Gotts, Thomas R Martin, Carolyn S Calfee, Michael A Matthay
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引用次数: 0

摘要

细菌性肺炎是急性呼吸窘迫综合征(ARDS)的常见病因,在活化的巨噬细胞、肺上皮细胞和内皮细胞释放的趋化因子的作用下,中性粒细胞是最先被招募到炎症部位的白细胞。虽然中性粒细胞炎症有助于消灭病原体,但中性粒细胞也可能造成旁观者组织损伤。尽管肺泡间隙中的中性粒细胞是急性肺损伤和 ARDS(尤其是肺炎引起的 ARDS)的一个主要特征,但它们对肺损伤发病机制的贡献尚不确定。本研究旨在阐明中性粒细胞在与临床相关的细菌性肺炎模型中的作用。我们研究了在用抗生素治疗的肺炎球菌肺炎小鼠模型中减少中性粒细胞的效果。在感染前 24 小时和感染前 24 小时,用抗 Ly6G 单克隆抗体减少中性粒细胞。小鼠经鼻内接种肺炎链球菌,并在接种细菌 12 小时后服用头孢曲松。与单独使用抗生素治疗相比,尽管肺远端气隙中的细菌量略有增加,但使用头孢曲松治疗的小鼠体内中性粒细胞的减少减轻了细菌性肺炎引起的低氧血症、肺泡通透性、上皮损伤、肺水肿和炎症生物标志物的释放。因此,如果使用适当的抗生素,细菌性肺炎早期阶段的肺损伤部分是由中性粒细胞介导的。在细菌性肺炎的早期阶段,虽然中性粒细胞也参与宿主防御,但它们对肺损伤的严重程度起着决定性作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neutrophil reduction attenuates the severity of lung injury in the early phase of pneumococcal pneumonia in mice.

Neutrophils are the first leukocytes to be recruited to sites of inflammation in response to chemotactic factors released by activated macrophages and pulmonary epithelial and endothelial cells in bacterial pneumonia, a common cause of acute respiratory distress syndrome (ARDS). Although neutrophilic inflammation facilitates the elimination of pathogens, neutrophils also may cause bystander tissue injury. Even though the presence of neutrophils in alveolar spaces is a key feature of acute lung injury and ARDS especially from pneumonia, their contribution to the pathogenesis of lung injury is uncertain. The goal of this study was to elucidate the role of neutrophils in a clinically relevant model of bacterial pneumonia. We investigated the effect of reducing neutrophils in a mouse model of pneumococcal pneumonia treated with antibiotics. Neutrophils were reduced with anti-lymphocyte antigen 6 complex locus G6D (Ly6G) monoclonal antibody 24 h before and immediately preceding infection. Mice were inoculated intranasally with Streptococcus pneumoniae and received ceftriaxone 12 h after bacterial inoculation. Neutrophil reduction in mice treated with ceftriaxone attenuated hypoxemia, alveolar permeability, epithelial injury, pulmonary edema, and inflammatory biomarker release induced by bacterial pneumonia, even though bacterial loads in the distal air spaces of the lung were modestly increased as compared with antibiotic treatment alone. Thus, when appropriate antibiotics are administered, lung injury in the early phase of bacterial pneumonia is mediated in part by neutrophils. In the early phase of bacterial pneumonia, neutrophils contribute to the severity of lung injury, although they also participate in host defense.NEW & NOTEWORTHY Neutrophil accumulation is a key feature of ARDS, but their contribution to the pathogenesis is still uncertain. We investigated the effect of reducing neutrophils in a clinically relevant mouse model of pneumococcal pneumonia treated with antibiotics. When appropriate antibiotics were administered, neutrophil reduction with Ly6G antibody markedly attenuated lung injury and improved oxygenation. In the early phase of bacterial pneumonia, neutrophils contribute to the severity of lung injury, although they also participate in host defense.

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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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