Taenaka Hiroki, Wick Katherine D, Sarma Aartik, Matsumoto Shotaro, Ghale Rajani, Fang Xiaohui, Maishan Mazharul, Gotts Jeffrey E, Langelier Charles R, Calfee Carolyn S, Matthay Michael A
University of California, San Francisco.
Mayo Clinic.
Res Sq. 2024 Feb 21:rs.3.rs-3962861. doi: 10.21203/rs.3.rs-3962861/v1.
is the most common bacterial cause of community acquired pneumonia and the acute respiratory distress syndrome (ARDS). Some clinical trials have demonstrated a beneficial effect of corticosteroid therapy in community acquired pneumonia, COVID-19, and ARDS, but the mechanisms of this benefit remain unclear. The objective of this study was to investigate the effects of corticosteroids on the pulmonary biology of pneumococcal pneumonia in an observational cohort of mechanically ventilated patients and in a mouse model of bacterial pneumonia with .
We studied gene expression with lower respiratory tract transcriptomes from a cohort of mechanically ventilated patients and in mice. We also carried out comprehensive physiologic, biochemical, and histological analyses in mice to identify the mechanisms of lung injury in with and without adjunctive steroid therapy.
Transcriptomic analysis identified pleiotropic effects of steroid therapy on the lower respiratory tract in critically ill patients with pneumococcal pneumonia, findings that were reproducible in mice. In mice with pneumonia, dexamethasone in combination with ceftriaxone reduced (1) pulmonary edema formation, (2) alveolar protein permeability, (3) proinflammatory cytokine release, (4) histopathologic lung injury score, and (5) hypoxemia but did not increase bacterial burden.
The gene expression studies in patients and in the mice support the clinical relevance of the mouse studies, which replicate several features of pneumococcal pneumonia and steroid therapy in humans. In combination with appropriate antibiotic therapy in mice, treatment of pneumococcal pneumonia with steroid therapy reduced hypoxemia, pulmonary edema, lung permeability, and histologic criteria of lung injury, and also altered inflammatory responses at the protein and gene expression level. The results from these studies provide evidence for the mechanisms that may explain the beneficial effects of glucocorticoid therapy in patients with community acquired pneumonia from .
是社区获得性肺炎和急性呼吸窘迫综合征(ARDS)最常见的细菌病因。一些临床试验已证明皮质类固醇疗法对社区获得性肺炎、COVID-19和ARDS有有益作用,但其益处的机制仍不清楚。本研究的目的是在机械通气患者的观察队列和伴有……的细菌性肺炎小鼠模型中研究皮质类固醇对肺炎球菌肺炎肺部生物学的影响。
我们研究了机械通气患者队列和小鼠下呼吸道转录组的基因表达。我们还对小鼠进行了全面的生理、生化和组织学分析,以确定在有和没有辅助类固醇治疗的情况下……肺损伤的机制。
转录组分析确定了类固醇疗法对重症肺炎球菌肺炎患者下呼吸道的多效性作用,这些发现在小鼠中可重复。在患有肺炎的小鼠中,地塞米松与头孢曲松联合使用可降低:(1)肺水肿形成;(2)肺泡蛋白通透性;(3)促炎细胞因子释放;(4)组织病理学肺损伤评分;(5)低氧血症,但不增加细菌负荷。
患者和小鼠的基因表达研究支持了小鼠研究的临床相关性,该研究复制了人类肺炎球菌肺炎和类固醇疗法的几个特征。在小鼠中,类固醇疗法与适当的抗生素治疗相结合,可降低低氧血症、肺水肿、肺通透性和肺损伤的组织学标准,并在蛋白质和基因表达水平上改变炎症反应。这些研究结果为可能解释糖皮质激素疗法对……社区获得性肺炎患者有益作用的机制提供了证据。