Vatsalya Vatsalya, Li Fengyuan, Frimodig Jane, Gala Khushboo S, Srivastava Shweta, Kong Maiying, Ramchandani Vijay A, Feng Wenke, Zhang Xiang, McClain Craig J
Department of Medicine, University of Louisville, Louisville, KY, United States.
Robley Rex VA Medical Center, Louisville, KY, United States.
Front Pharmacol. 2021 Mar 2;11:598128. doi: 10.3389/fphar.2020.598128. eCollection 2020.
Coronavirus disease identified in 2019 (COVID-19) can be complicated by the Th17 cell-mediated IL-17 proinflammatory response. We tested if thiamine can effectively lower the Th17 response in a clinical study [Proinflammatory state in alcohol use disorder patients termed as disease controls (DC)] and corroborated the results using an study. We developed an effective dose range and model for key pharmacokinetic measures with the potential of targeting the cytokine storm and neurological symptoms of COVID-19. Three-week 200 mg dose of thiamine was administered to sixteen DC patients. Eight healthy volunteers (HV) were also included in this investigation. A subsequent study was performed to validate the effectiveness of thiamine [100 mg/day equivalent (0.01 μg/ml)] treatment in lowering the Th17 proinflammatory response in a mouse macrophage cell line (RAW264.7) treated with ethanol. Based on recent publications, we compared the results of the IL-17 response from our clinical and study to those found in other proinflammatory disease conditions (metabolic conditions, septic shock, viral infections and COVID-19) and effective and safe dose ranges of thiamine. We developed a pharmacokinetic profile for thiamine dose range as a novel intervention strategy in COVID-19. DC group showed significantly elevated proinflammatory cytokines compared to HV. Thiamine-treated DC patients showed significant lowering in IL-17 and increase in the IL-22 levels. In humans, a range of 79-474 mg daily of thiamine was estimated to be effective and safe as an intervention for the COVID-19 cytokine storm. A literature review showed that several neurological symptoms of COVID-19 (∼45.5% of the severe cases) occur in other viral infections and neuroinflammatory states that may also respond to thiamine treatment. Thiamine, a very safe drug even at very high doses, could be repurposed for treating the Th17 mediated IL-17 immune storm, and the subsequent neurological symptoms observed in COVID-19. Further studies using thiamine as an intervention/prevention strategy in COVID-19 patients could identify its precise anti-inflammatory role.
2019年发现的冠状病毒病(COVID-19)可能会因Th17细胞介导的IL-17促炎反应而复杂化。我们在一项临床研究[将酒精使用障碍患者的促炎状态称为疾病对照(DC)]中测试了硫胺素是否能有效降低Th17反应,并使用一项研究证实了结果。我们开发了一个有效的剂量范围和关键药代动力学指标模型,其有可能针对COVID-19的细胞因子风暴和神经症状。对16名DC患者给予为期三周的200毫克硫胺素剂量。本研究还纳入了8名健康志愿者(HV)。随后进行了一项研究,以验证硫胺素[100毫克/天当量(0.01微克/毫升)]治疗在降低用乙醇处理的小鼠巨噬细胞系(RAW264.7)中Th17促炎反应方面的有效性。基于最近的出版物,我们将我们的临床研究和研究中IL-17反应的结果与其他促炎疾病状况(代谢状况、脓毒症休克、病毒感染和COVID-19)以及硫胺素有效和安全剂量范围的结果进行了比较。我们开发了硫胺素剂量范围的药代动力学概况,作为COVID-19中的一种新型干预策略。与HV相比,DC组的促炎细胞因子显著升高。硫胺素治疗的DC患者IL-17显著降低,IL-22水平升高。在人类中,估计每天79-474毫克的硫胺素作为COVID-19细胞因子风暴的干预措施是有效和安全的。文献综述表明,COVID-19的几种神经症状(约45.5%的重症病例)发生在其他病毒感染和神经炎症状态中,这些状态也可能对硫胺素治疗有反应。硫胺素是一种即使在非常高的剂量下也非常安全的药物,可以重新用于治疗Th17介导的IL-17免疫风暴以及在COVID-19中观察到的随后的神经症状。在COVID-19患者中使用硫胺素作为干预/预防策略的进一步研究可以确定其确切的抗炎作用。