Azabou Eric, Bao Guillaume, Bounab Rania, Heming Nicholas, Annane Djillali
Clinical Neurophysiology and Neuromodulation Unit, Departments of Physiology and Critical Care Medicine, Raymond Poincaré Hospital, Assistance Publique- Hôpitaux de Paris, Inserm UMR 1173, Infection and Inflammation (2I), University of Versailles Saint-Quentin en Yvelines (UVSQ), Paris-Saclay University, Paris, France.
General Intensive Care Unit - Assistance Publique Hôpitaux de Paris, Raymond Poincaré Hospital, Assistance Publique- Hôpitaux de Paris, Inserm UMR 1173, Infection and Inflammation (2I), University of Versailles Saint-Quentin en Yvelines (UVSQ), Paris-Saclay University, Paris, France.
Front Med (Lausanne). 2021 May 7;8:625836. doi: 10.3389/fmed.2021.625836. eCollection 2021.
The novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) causes coronavirus disease 2019 (COVID-19) through excessive end organ inflammation. Despite improved understanding of the pathophysiology, management, and the great efforts worldwide to produce effective drugs, death rates of COVID-19 patients remain unacceptably high, and effective treatment is unfortunately lacking. Pharmacological strategies aimed at modulating inflammation in COVID-19 are being evaluated worldwide. Several drug therapies targeting this excessive inflammation, such as tocilizumab, an interleukin (IL)-6 inhibitor, corticosteroids, programmed cell death protein (PD)-1/PD-L1 checkpoint inhibition, cytokine-adsorption devices, and intravenous immunoglobulin have been identified as potentially useful and reliable approaches to counteract the cytokine storm. However, little attention is currently paid for non-drug therapeutic strategies targeting inflammatory and immunological processes that may be useful for reducing COVID-19-induced complications and improving patient outcome. Vagus nerve stimulation attenuates inflammation both in experimental models and preliminary data in human. Modulating the activity of cholinergic anti-inflammatory pathways (CAPs) described by the group of KJ Tracey has indeed become an important target of therapeutic research strategies for inflammatory diseases and sepsis. Non-invasive transcutaneous vagal nerve stimulation (t-VNS), as a non-pharmacological adjuvant, may help reduce the burden of COVID-19 and deserve to be investigated. VNS as an adjunct therapy in COVID-19 patients should be investigated in clinical trials. Two clinical trials on this topic are currently underway (NCT04382391 and NCT04368156). The results of these trials will be informative, but additional larger studies are needed.
新型严重急性呼吸综合征冠状病毒2(SARS-CoV-2)通过终末器官的过度炎症反应引发2019冠状病毒病(COVID-19)。尽管对其病理生理学和治疗方法的认识有所提高,并且全球都在努力研发有效药物,但COVID-19患者的死亡率仍然高得令人无法接受,而且遗憾的是缺乏有效的治疗方法。全球正在评估旨在调节COVID-19炎症反应的药理学策略。几种针对这种过度炎症反应的药物疗法,如白细胞介素(IL)-6抑制剂托珠单抗、皮质类固醇、程序性细胞死亡蛋白(PD)-1/PD-L1检查点抑制剂、细胞因子吸附装置和静脉注射免疫球蛋白,已被确定为对抗细胞因子风暴的潜在有用且可靠的方法。然而,目前针对可能有助于减少COVID-19引起的并发症并改善患者预后的炎症和免疫过程的非药物治疗策略关注较少。迷走神经刺激在实验模型和人体初步数据中均可减轻炎症。调节KJ Tracey团队描述的胆碱能抗炎通路(CAPs)的活性确实已成为炎症性疾病和脓毒症治疗研究策略的重要靶点。非侵入性经皮迷走神经刺激(t-VNS)作为一种非药物辅助手段,可能有助于减轻COVID-19的负担,值得研究。迷走神经刺激作为COVID-19患者的辅助治疗应在临床试验中进行研究。目前有两项关于该主题的临床试验正在进行中(NCT04382391和NCT04368156)。这些试验的结果将提供信息,但还需要更多更大规模的研究。