Flipped Inflammatory Time and the Role of Antibodies Against Severe Acute Respiratory Syndrome Coronavirus 2: Optimizing Tocilizumab Against Coronavirus Disease 2019.
Pablo Guisado VascoJosé Aguarles GorinesMaría M Carralón GonzálezGabriel Sotres FernándezDaniel Carnevali RuizPublished in: The Journal of infectious diseases (2022)
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.
Keyphrases
- respiratory syndrome coronavirus
- coronavirus disease
- sars cov
- open label
- immune response
- phase iii
- risk factors
- clinical trial
- rheumatoid arthritis
- type diabetes
- oxidative stress
- coronary artery disease
- high throughput
- case report
- cardiovascular disease
- rectal cancer
- small molecule
- phase ii study
- protein protein
- drug induced