<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>111</volume><submitter>Perricone C</submitter><pubmed_abstract>The outbreak of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has posed the world at a pandemic risk. Coronavirus-19 disease (COVID-19) is an infectious disease caused by SARS-CoV-2, which causes pneumonia, requires intensive care unit hospitalization in about 10% of cases and can lead to a fatal outcome. Several efforts are currently made to find a treatment for COVID-19 patients. So far, several anti-viral and immunosuppressive or immunomodulating drugs have demonstrated some efficacy on COVID-19 both in vitro and in animal models as well as in cases series. In COVID-19 patients a pro-inflammatory status with high levels of interleukin (IL)-1B, IL-1 receptor (R)A and tumor necrosis factor (TNF)-? has been demonstrated. Moreover, high levels of IL-6 and TNF-? have been observed in patients requiring intensive-care-unit hospitalization. This provided rationale for the use of anti-rheumatic drugs as potential treatments for this severe viral infection. Other agents, such as hydroxychloroquine and chloroquine might have a direct anti-viral effect. The anti-viral aspect of immunosuppressants towards a variety of viruses has been known since long time and it is herein discussed in the view of searching for a potential treatment for SARS-CoV-2 infection.</pubmed_abstract><journal>Journal of autoimmunity</journal><pagination>102468</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7164894</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The anti-viral facet of anti-rheumatic drugs: Lessons from COVID-19.</pubmed_title><pmcid>PMC7164894</pmcid><pubmed_authors>Triggianese P</pubmed_authors><pubmed_authors>Perricone C</pubmed_authors><pubmed_authors>Perricone R</pubmed_authors><pubmed_authors>Cafaro G</pubmed_authors><pubmed_authors>Bursi R</pubmed_authors><pubmed_authors>Bartoloni E</pubmed_authors><pubmed_authors>Bonifacio AF</pubmed_authors><pubmed_authors>Gerli R</pubmed_authors></additional><is_claimable>false</is_claimable><name>The anti-viral facet of anti-rheumatic drugs: Lessons from COVID-19.</name><description>The outbreak of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has posed the world at a pandemic risk. Coronavirus-19 disease (COVID-19) is an infectious disease caused by SARS-CoV-2, which causes pneumonia, requires intensive care unit hospitalization in about 10% of cases and can lead to a fatal outcome. Several efforts are currently made to find a treatment for COVID-19 patients. So far, several anti-viral and immunosuppressive or immunomodulating drugs have demonstrated some efficacy on COVID-19 both in vitro and in animal models as well as in cases series. In COVID-19 patients a pro-inflammatory status with high levels of interleukin (IL)-1B, IL-1 receptor (R)A and tumor necrosis factor (TNF)-? has been demonstrated. Moreover, high levels of IL-6 and TNF-? have been observed in patients requiring intensive-care-unit hospitalization. This provided rationale for the use of anti-rheumatic drugs as potential treatments for this severe viral infection. Other agents, such as hydroxychloroquine and chloroquine might have a direct anti-viral effect. The anti-viral aspect of immunosuppressants towards a variety of viruses has been known since long time and it is herein discussed in the view of searching for a potential treatment for SARS-CoV-2 infection.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2021-02-20T04:11:46Z</modification><creation>2020-05-22T18:08:40Z</creation></dates><accession>S-EPMC7164894</accession><cross_references><pubmed>32317220</pubmed><doi>10.1016/j.jaut.2020.102468</doi></cross_references></HashMap>