<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Torres M</submitter><funding>Instituto de Salud Carlos III</funding><funding>NIAID NIH HHS</funding><funding>España Ministerio de Ciencia e Innovación</funding><pagination>112965</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9008199</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>150</volume><pubmed_abstract>Main cause of severe illness and death in COVID-19 patients appears to be an excessive but ineffectual inflammatory immune response that may cause severe acute respiratory distress syndrome (ARDS). Vitamin D may favour an anti-inflammatory environment and improve cytotoxic response against some infectious diseases. A multicenter, single-blind, prospective, randomized clinical trial was approved in patients with COVID-19 pneumonia and levels of 25-hydroxyvitamin D (25(OH)D) of 14.8 ng/ml (SD: 6.18) to test antiviral efficacy, tolerance and safety of 10,000 IU/day of cholecalciferol (vitamin D&lt;sub>3&lt;/sub>) for 14 days, in comparison with 2000 IU/day. After supplementation, mean serum 25(OH)D levels increased to 19 ng/ml on average in 2000 IU/day versus 29 ng/ml in 10,000 IU/day group (p &lt; 0.</pubmed_abstract><journal>Biomedicine &amp; pharmacotherapy = Biomedecine &amp; pharmacotherapie</journal><pubmed_title>Changes in the immune response against SARS-CoV-2 in individuals with severe COVID-19 treated with high dose of vitamin D.</pubmed_title><pmcid>PMC9008199</pmcid><funding_grant_id>R01 AI143567</funding_grant_id><pubmed_authors>Mateos E</pubmed_authors><pubmed_authors>Taboada-Martinez ML</pubmed_authors><pubmed_authors>Patricia Fernandez Fernandez C</pubmed_authors><pubmed_authors>Pardo Guimera V</pubmed_authors><pubmed_authors>Jose Martinez Martin E</pubmed_authors><pubmed_authors>Contributing members of the Multidisciplinary Group of Study of COVID-19 (in alphabetical order)</pubmed_authors><pubmed_authors>Garcia Lacalle C</pubmed_authors><pubmed_authors>Multidisciplinary Group of Study of COVID-19 (MGS-COVID)</pubmed_authors><pubmed_authors>Cascajero Diaz A</pubmed_authors><pubmed_authors>Carrillo Blanco G</pubmed_authors><pubmed_authors>Martin Sagarra O</pubmed_authors><pubmed_authors>Renuncio Garcia D</pubmed_authors><pubmed_authors>Ramos-Martin F</pubmed_authors><pubmed_authors>Torres Perea R</pubmed_authors><pubmed_authors>Javier Martinez Simon J</pubmed_authors><pubmed_authors>Sanz-Moreno J</pubmed_authors><pubmed_authors>Teresa Chica Burguillo M</pubmed_authors><pubmed_authors>Diez Vinas V</pubmed_authors><pubmed_authors>Arevalo Camacho S</pubmed_authors><pubmed_authors>Sanz Moreno J</pubmed_authors><pubmed_authors>Lopez-Wolf D</pubmed_authors><pubmed_authors>Rodriguez-Mora S</pubmed_authors><pubmed_authors>Fernandez Mondelo Y</pubmed_authors><pubmed_authors>Lucena Campillo A</pubmed_authors><pubmed_authors>Luisa Pinillos Pardo M</pubmed_authors><pubmed_authors>Velasco Arribas M</pubmed_authors><pubmed_authors>Valencia La Rosa J</pubmed_authors><pubmed_authors>Corrochano Garcia A</pubmed_authors><pubmed_authors>Torres M</pubmed_authors><pubmed_authors>Alonso-Menchen D</pubmed_authors><pubmed_authors>Blanca Lopez N</pubmed_authors><pubmed_authors>Fonseca Aizpuri E</pubmed_authors><pubmed_authors>Garcia-Perez J</pubmed_authors><pubmed_authors>Roger Revilla A</pubmed_authors><pubmed_authors>Matarranz Del Amo M</pubmed_authors><pubmed_authors>Casado G</pubmed_authors><pubmed_authors>Lopez-Huertas MR</pubmed_authors><pubmed_authors>Helguera Amezua C</pubmed_authors><pubmed_authors>Gomez-Alvarez Dominguez M</pubmed_authors><pubmed_authors>Novella-Mena M</pubmed_authors><pubmed_authors>Vigon L</pubmed_authors><pubmed_authors>Ryan-Murua P</pubmed_authors><pubmed_authors>Angeles Rodriguez Davila M</pubmed_authors><pubmed_authors>Sampablo Valverde L</pubmed_authors><pubmed_authors>Canamares Orbis I</pubmed_authors><pubmed_authors>Ramirez Fuentes FA</pubmed_authors><pubmed_authors>Cervero M</pubmed_authors><pubmed_authors>Jose Hidalgo Correas F</pubmed_authors><pubmed_authors>Villanueva Fernandez-Ardavin A</pubmed_authors><pubmed_authors>Coiras M</pubmed_authors><pubmed_authors>Corredera Garcia S</pubmed_authors><pubmed_authors>Avila Calzada C</pubmed_authors><pubmed_authors>Antonio Barbado Albaladejo J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Changes in the immune response against SARS-CoV-2 in individuals with severe COVID-19 treated with high dose of vitamin D.</name><description>Main cause of severe illness and death in COVID-19 patients appears to be an excessive but ineffectual inflammatory immune response that may cause severe acute respiratory distress syndrome (ARDS). Vitamin D may favour an anti-inflammatory environment and improve cytotoxic response against some infectious diseases. A multicenter, single-blind, prospective, randomized clinical trial was approved in patients with COVID-19 pneumonia and levels of 25-hydroxyvitamin D (25(OH)D) of 14.8 ng/ml (SD: 6.18) to test antiviral efficacy, tolerance and safety of 10,000 IU/day of cholecalciferol (vitamin D&lt;sub>3&lt;/sub>) for 14 days, in comparison with 2000 IU/day. After supplementation, mean serum 25(OH)D levels increased to 19 ng/ml on average in 2000 IU/day versus 29 ng/ml in 10,000 IU/day group (p &lt; 0.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jun</publication><modification>2025-05-18T10:52:48.89Z</modification><creation>2024-10-17T18:32:02.461Z</creation></dates><accession>S-EPMC9008199</accession><cross_references><pubmed>35468580</pubmed><doi>10.1016/j.biopha.2022.112965</doi></cross_references></HashMap>