Immunomodulation as Treatment for Severe Coronavirus Disease 2019: A Systematic Review of Current Modalities and Future Directions.
Eric A MeyerowitzPritha SenSara R SchoenfeldTomas G NeilanMatthew J FrigaultJohn H StoneArthur Y KimMichael K MansourPublished in: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America (2021)
In severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, viral load peaks early and declines quickly after symptom onset. Severe coronavirus disease 2019 (COVID-19) is marked by aberrant innate and adaptive immune responses with an abnormal cytokine profile and multiorgan system dysfunction that persists well after viral clearance. A purely antiviral treatment strategy may therefore be insufficient, and antiviral agents have not shown a benefit later in the illness course. A number of immunomodulatory strategies are being tested, including corticosteroids, cytokine and anticytokine therapies, small molecule inhibitors, and cellular therapeutics. To date, the only drug to show a mortality benefit for COVID-19 in a randomized, controlled trial is dexamethasone. However, there remains uncertainty about which patients may benefit most and about longer-term complications, including secondary infections. Here, we review the immune dysregulation of severe COVID-19 and the existing data behind various immunomodulatory strategies, and we consider future directions of study.
Keyphrases
- coronavirus disease
- respiratory syndrome coronavirus
- sars cov
- small molecule
- immune response
- early onset
- ejection fraction
- current status
- electronic health record
- newly diagnosed
- preterm infants
- risk factors
- low dose
- cardiovascular events
- dendritic cells
- high dose
- inflammatory response
- protein protein
- adverse drug
- gestational age
- preterm birth
- machine learning
- deep learning