Flipped Inflammatory Time and the Role of Antibodies Against Severe Acute Respiratory Syndrome Coronavirus 2: Optimizing Tocilizumab Against Coronavirus Disease 2019

P. Guisado-Vasco, José Aguarles Gorines, M. M. Carralón González, G. Sotres Fernández, D. Carnevali Ruiz
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Abstract

Abstract Use of interleukin (IL-6) inhibitors has become one of the most complicated clinical issues in treating coronavirus disease 2019 (COVID-19). Recently, randomized open-label platform trials have found that IL-6 inhibitors have a beneficial effect on mortality in severe COVID-19. However, several questions arise around their mechanism of action in this disease, as well as how, when, and at which dose they should be used. IL-6 has both proinflammatory and anti-inflammatory effects, which may modulate the course of COVID-19, whose immunopathogenesis is driven by the innate immune system, autoantibodies, and interferon. Given that patients with delayed seroconversion against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein would be at the highest risk of complications beyond the second week of disease, we propose that considering patient serostatus at admission could optimize the use of IL-6 inhibitors in COVID-19. We predict that the net treatment benefits could be higher in the subgroup of patients with delayed seroconversion as compared to those who seroconvert more rapidly after SARS-CoV-2 infection.
翻转炎症时间和抗严重急性呼吸综合征冠状病毒抗体2的作用:优化托珠单抗抗冠状病毒病2019
白细胞介素(IL-6)抑制剂的使用已成为治疗冠状病毒病(COVID-19)最复杂的临床问题之一。最近,随机开放标签平台试验发现,IL-6抑制剂对重症COVID-19患者的死亡率有有益影响。然而,围绕它们在这种疾病中的作用机制,以及如何、何时和以何种剂量使用,出现了一些问题。IL-6具有促炎和抗炎双重作用,可能调节COVID-19的病程,其免疫发病机制由先天免疫系统、自身抗体和干扰素驱动。鉴于严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)刺突蛋白血清转化延迟的患者在发病第二周后出现并发症的风险最高,我们建议考虑患者入院时的血清状态,可以优化COVID-19中IL-6抑制剂的使用。我们预测,与SARS-CoV-2感染后血清转化更快的患者相比,血清转化延迟的患者亚组的净治疗效益可能更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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