<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Slominski RM</submitter><funding>BLRD VA</funding><funding>NIAID NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>VA</funding><funding>NIAMS NIH HHS</funding><funding>NIH HHS</funding><pagination>885-890</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7436895</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>29(9)</volume><pubmed_abstract>The negative outcomes of COVID-19 diseases respiratory distress (ARDS) and the damage to other organs are secondary to a "cytokine storm" and to the attendant oxidative stress. Active hydroxyl forms of vitamin D are anti-inflammatory, induce antioxidative responses, and stimulate innate immunity against infectious agents. These properties are shared by calcitriol and the CYP11A1-generated non-calcemic hydroxyderivatives. They inhibit the production of pro-inflammatory cytokines, downregulate NF-κΒ, show inverse agonism on RORγ and counteract oxidative stress through the activation of NRF-2. Therefore, a direct delivery of hydroxyderivatives of vitamin D deserves consideration in the treatment of COVID-19 or ARDS of different aetiology. We also recommend treatment of COVID-19 patients with </pubmed_abstract><journal>Experimental dermatology</journal><pubmed_title>COVID-19 and Vitamin D: A lesson from the skin.</pubmed_title><pmcid>PMC7436895</pmcid><funding_grant_id>R01 AR073004</funding_grant_id><funding_grant_id>R01 AR071189</funding_grant_id><funding_grant_id>R21 AI149267</funding_grant_id><funding_grant_id>1R21AI149267-01A1</funding_grant_id><funding_grant_id>1R01AR073004</funding_grant_id><funding_grant_id>R21 MD015319</funding_grant_id><funding_grant_id>1I01BX004293-01A1</funding_grant_id><funding_grant_id>I01 BX004293</funding_grant_id><funding_grant_id>R01AR071189</funding_grant_id><pubmed_authors>Stefan J</pubmed_authors><pubmed_authors>Slominski AT</pubmed_authors><pubmed_authors>Raman C</pubmed_authors><pubmed_authors>Athar M</pubmed_authors><pubmed_authors>Jetten AM</pubmed_authors><pubmed_authors>Holick MF</pubmed_authors><pubmed_authors>Slominski RM</pubmed_authors></additional><is_claimable>false</is_claimable><name>COVID-19 and Vitamin D: A lesson from the skin.</name><description>The negative outcomes of COVID-19 diseases respiratory distress (ARDS) and the damage to other organs are secondary to a "cytokine storm" and to the attendant oxidative stress. Active hydroxyl forms of vitamin D are anti-inflammatory, induce antioxidative responses, and stimulate innate immunity against infectious agents. These properties are shared by calcitriol and the CYP11A1-generated non-calcemic hydroxyderivatives. They inhibit the production of pro-inflammatory cytokines, downregulate NF-κΒ, show inverse agonism on RORγ and counteract oxidative stress through the activation of NRF-2. Therefore, a direct delivery of hydroxyderivatives of vitamin D deserves consideration in the treatment of COVID-19 or ARDS of different aetiology. We also recommend treatment of COVID-19 patients with </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2026-05-02T22:18:18.034Z</modification><creation>2022-07-19T07:47:22.391Z</creation></dates><accession>S-EPMC7436895</accession><cross_references><pubmed>32779213</pubmed><doi>10.1111/exd.14170</doi></cross_references></HashMap>