Coronavirus Disease 2019: Investigational Therapies in the Prevention and Treatment of Hyperinflammation
Overview
Authors
Affiliations
: The mortality of coronavirus disease 2019 (COVID-19) is frequently driven by an injurious immune response characterized by the development of acute respiratory distress syndrome (ARDS), endotheliitis, coagulopathy, and multi-organ failure. This spectrum of hyperinflammation in COVID-19 is commonly referred to as cytokine storm syndrome (CSS). : Medline and Google Scholar were searched up until 15th of August 2020 for relevant literature. Evidence supports a role of dysregulated immune responses in the immunopathogenesis of severe COVID-19. CSS associated with SARS-CoV-2 shows similarities to the exuberant cytokine production in some patients with viral infection (e.g.SARS-CoV-1) and may be confused with other syndromes of hyperinflammation like the cytokine release syndrome (CRS) in CAR-T cell therapy. Interleukin (IL)-6, IL-8, and tumor necrosis factor-alpha have emerged as predictors of COVID-19 severity and in-hospital mortality. : Despite similarities, COVID-19-CSS appears to be distinct from HLH, MAS, and CRS, and the application of HLH diagnostic scores and criteria to COVID-19 is not supported by emerging data. While immunosuppressive therapy with glucocorticoids has shown a mortality benefit, cytokine inhibitors may hold promise as 'rescue therapies' in severe COVID-19. Given the arguably limited benefit in advanced disease, strategies to prevent the development of COVID-19-CSS are needed.
Rutskaya-Moroshan K, Abisheva S, Abisheva A, Amangeldiyeva Z, Vinnik T, Batyrkhan T Medicina (Kaunas). 2024; 60(9).
PMID: 39336418 PMC: 11433992. DOI: 10.3390/medicina60091377.
Xu Y, Huang Z, Wu G, Jin F, Lin S, Zhang C Comput Methods Programs Biomed. 2023; 238:107584.
PMID: 37207464 PMC: 10156651. DOI: 10.1016/j.cmpb.2023.107584.
Immune responses in mildly versus critically ill COVID-19 patients.
Nasrollahi H, Talepoor A, Saleh Z, Vakili M, Heydarinezhad P, Karami N Front Immunol. 2023; 14:1077236.
PMID: 36793739 PMC: 9923185. DOI: 10.3389/fimmu.2023.1077236.
Venegas-Rodriguez R, Serrano-Diaz A, Pena-Ruiz R, Santana-Sanchez R, Hernandez-Cedeno M, Rittoles Navarro A PLoS One. 2023; 18(2):e0281111.
PMID: 36730325 PMC: 9894446. DOI: 10.1371/journal.pone.0281111.
Diabetes-Modifying Antirheumatic Drugs: The Roles of DMARDs as Glucose-Lowering Agents.
Infante M, Padilla N, Alejandro R, Caprio M, Della-Morte D, Fabbri A Medicina (Kaunas). 2022; 58(5).
PMID: 35629988 PMC: 9143119. DOI: 10.3390/medicina58050571.