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超声脾脏神经调节在肺炎模型中具有时间依赖性抗炎作用。

Ultrasound Neuromodulation of the Spleen Has Time-Dependent Anti-Inflammatory Effect in a Pneumonia Model.

机构信息

Institute of Bioelectronic Medicine, Feinstein Institutes for Medical Research, Manhasset, NY, United States.

General Electric Research, Niskayuna, NY, United States.

出版信息

Front Immunol. 2022 Jun 16;13:892086. doi: 10.3389/fimmu.2022.892086. eCollection 2022.

DOI:10.3389/fimmu.2022.892086
PMID:35784337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9244783/
Abstract

Interfaces between the nervous and immune systems have been shown essential for the coordination and regulation of immune responses. Non-invasive ultrasound stimulation targeted to the spleen has recently been shown capable of activating one such interface, the splenic cholinergic anti-inflammatory pathway (CAP). Over the past decade, CAP and other neuroimmune pathways have been activated using implanted nerve stimulators and tested to prevent cytokine release and inflammation. However, CAP studies have typically been performed in models of severe, systemic (e.g., endotoxemia) or chronic inflammation (e.g., collagen-induced arthritis or DSS-induced colitis). Herein, we examined the effects of activation of the splenic CAP with ultrasound in a model of local bacterial infection by lung instillation of 10 CFU of Streptococcus pneumoniae. We demonstrate a time-dependent effect of CAP activation on the cytokine response assay during infection progression. CAP activation-induced cytokine suppression is absent at intermediate times post-infection (16 hours following inoculation), but present during the early (4 hours) and later phases (48 hours). These results indicate that cytokine inhibition associated with splenic CAP activation is not observed at all timepoints following bacterial infection and highlights the importance of further studying neuroimmune interfaces within the context of different immune system and inflammatory states.

摘要

神经系统和免疫系统之间的相互作用对于协调和调节免疫反应至关重要。最近的研究表明,针对脾脏的非侵入性超声刺激能够激活一种这样的界面,即脾脏胆碱能抗炎途径 (CAP)。在过去的十年中,已经使用植入式神经刺激器激活了 CAP 和其他神经免疫途径,并对其进行了测试,以防止细胞因子释放和炎症。然而,CAP 研究通常在严重的全身性炎症(例如内毒素血症)或慢性炎症(例如胶原诱导性关节炎或 DSS 诱导的结肠炎)模型中进行。在此,我们通过肺部滴注 10 CFU 肺炎链球菌研究了用超声激活脾脏 CAP 在局部细菌感染模型中的作用。我们在感染进展过程中观察到 CAP 激活对细胞因子反应测定的时间依赖性影响。CAP 激活诱导的细胞因子抑制在感染后中间时间点(接种后 16 小时)不存在,但在早期(4 小时)和晚期(48 小时)存在。这些结果表明,在细菌感染后并非所有时间点都观察到与脾脏 CAP 激活相关的细胞因子抑制,这突出了在不同的免疫系统和炎症状态下进一步研究神经免疫界面的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/6cf68c8778c1/fimmu-13-892086-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/61b3a6c1bd24/fimmu-13-892086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/c0da079b413d/fimmu-13-892086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/7ed9c66d7d46/fimmu-13-892086-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/6cf68c8778c1/fimmu-13-892086-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/61b3a6c1bd24/fimmu-13-892086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/c0da079b413d/fimmu-13-892086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/7ed9c66d7d46/fimmu-13-892086-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d06b/9244783/6cf68c8778c1/fimmu-13-892086-g004.jpg

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