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Cell Metab ; 32(5): 704-709, 2020 11 03.
Article in English | MEDLINE | ID: covidwho-753751

ABSTRACT

SARS-CoV-2 pneumonitis can quickly strike to incapacitate the lung, leading to severe disease and sometimes death. In this perspective, we suggest that vitamin D deficiency and the failure to activate the vitamin D receptor (VDR) can aggravate this respiratory syndrome by igniting a wounding response in stellate cells of the lung. The FDA-approved injectable vitamin D analog, paricalcitol, suppresses stellate cell-derived murine hepatic and pancreatic pro-inflammatory and pro-fibrotic changes. Therefore, we suggest a possible parallel program in the pulmonary stellate cells of COVID-19 patients and propose repurposing paricalcitol infusion therapy to restrain the COVID-19 cytokine storm. This proposed therapy could prove important to people of color who have higher COVID-19 mortality rates and lower vitamin D levels.


Subject(s)
Betacoronavirus , Coronavirus Infections/drug therapy , Drug Repositioning/methods , Ergocalciferols/pharmacology , Ergocalciferols/therapeutic use , Pneumonia, Viral/drug therapy , Receptors, Calcitriol/agonists , Wound Healing/drug effects , Animals , COVID-19 , Coronavirus Infections/immunology , Coronavirus Infections/virology , Cytokines/metabolism , Humans , Mice , Pandemics , Pneumonia, Viral/immunology , Pneumonia, Viral/virology , Receptors, Calcitriol/metabolism , SARS-CoV-2 , Vitamin D Deficiency/drug therapy , Vitamin D Deficiency/epidemiology
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