Abstract
Cytokine release and macrophage activation contribute to immunopathology after SARS-CoV-2 infection. We discuss approaches to decrease the morbidity and mortality in patients with COVID-19 by repurposing existing drugs previously developed for cancer therapy.
©2020 American Association for Cancer Research.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Animals
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Betacoronavirus*
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COVID-19
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Calcineurin Inhibitors / therapeutic use
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Cell- and Tissue-Based Therapy
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Coronavirus Infections / complications*
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Coronavirus Infections / epidemiology
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Cytokines / metabolism
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Drug Repositioning
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Humans
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Immunotherapy / methods*
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Inflammation / epidemiology
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Inflammation / etiology
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Inflammation / therapy*
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Lymphohistiocytosis, Hemophagocytic / etiology
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Lymphohistiocytosis, Hemophagocytic / prevention & control
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Lymphohistiocytosis, Hemophagocytic / therapy
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Macrophage Activation
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Morbidity
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Neoplasms / therapy
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Neoplasms / virology
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Pandemics
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Pneumonia, Viral / complications*
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Pneumonia, Viral / epidemiology
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Receptors, Antigen, T-Cell / immunology
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SARS-CoV-2
Substances
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Calcineurin Inhibitors
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Cytokines
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Receptors, Antigen, T-Cell