<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Favalli A</submitter><funding>Regione Lombardia</funding><funding>Ministero della Salute</funding><funding>Fondazione Romeo ed Enrica Invernizzi</funding><pubmed_abstract>COVID-19 has proven to be particularly serious and life-threatening for patients presenting with pre-existing pathologies. Patients affected by rheumatic musculoskeletal disease (RMD) are likely to have impaired immune responses against SARS-CoV-2 infection due to their compromised immune system and the prolonged use of disease-modifying anti-rheumatic drugs (DMARDs), which include conventional synthetic (cs) DMARDs or biologic and targeted synthetic (b/ts) DMARDs. To provide an integrated analysis of the immune response following SARS-CoV-2 infection in RMD patients treated with different classes of DMARDs we carried out an immunological analysis of the antibody responses toward SARS-CoV-2 nucleocapsid and RBD proteins and an extensive immunophenotypic analysis of the major immune cell po</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>873195</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9226581</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Immunosuppressant Treatment in Rheumatic Musculoskeletal Diseases Does Not Inhibit Elicitation of Humoral Response to SARS-CoV-2 Infection and Preserves Effector Immune Cell Populations.</pubmed_title><pmcid>PMC9226581</pmcid><pubmed_authors>Favalli EG</pubmed_authors><pubmed_authors>Fabbris T</pubmed_authors><pubmed_authors>Pesce E</pubmed_authors><pubmed_authors>Gobbini A</pubmed_authors><pubmed_authors>Caporali R</pubmed_authors><pubmed_authors>Maioli G</pubmed_authors><pubmed_authors>Granucci F</pubmed_authors><pubmed_authors>Bandera A</pubmed_authors><pubmed_authors>Favalli A</pubmed_authors><pubmed_authors>Sarnicola ML</pubmed_authors><pubmed_authors>De Francesco R</pubmed_authors><pubmed_authors>Donnici L</pubmed_authors><pubmed_authors>Gori A</pubmed_authors><pubmed_authors>Grifantini R</pubmed_authors><pubmed_authors>Martinovic M</pubmed_authors><pubmed_authors>Gruarin P</pubmed_authors><pubmed_authors>Notarbartolo S</pubmed_authors><pubmed_authors>Manganaro L</pubmed_authors><pubmed_authors>Curti S</pubmed_authors><pubmed_authors>Biggioggero M</pubmed_authors><pubmed_authors>Marongiu L</pubmed_authors><pubmed_authors>Abrignani S</pubmed_authors><pubmed_authors>Zagato E</pubmed_authors><pubmed_authors>Bevilacqua V</pubmed_authors><pubmed_authors>Bombaci M</pubmed_authors><pubmed_authors>Crosti M</pubmed_authors><pubmed_authors>Marchisio E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunosuppressant Treatment in Rheumatic Musculoskeletal Diseases Does Not Inhibit Elicitation of Humoral Response to SARS-CoV-2 Infection and Preserves Effector Immune Cell Populations.</name><description>COVID-19 has proven to be particularly serious and life-threatening for patients presenting with pre-existing pathologies. Patients affected by rheumatic musculoskeletal disease (RMD) are likely to have impaired immune responses against SARS-CoV-2 infection due to their compromised immune system and the prolonged use of disease-modifying anti-rheumatic drugs (DMARDs), which include conventional synthetic (cs) DMARDs or biologic and targeted synthetic (b/ts) DMARDs. To provide an integrated analysis of the immune response following SARS-CoV-2 infection in RMD patients treated with different classes of DMARDs we carried out an immunological analysis of the antibody responses toward SARS-CoV-2 nucleocapsid and RBD proteins and an extensive immunophenotypic analysis of the major immune cell po</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-27T20:19:28.973Z</modification><creation>2024-11-15T12:44:29.064Z</creation></dates><accession>S-EPMC9226581</accession><cross_references><pubmed>35757699</pubmed><doi>10.3389/fimmu.2022.873195</doi></cross_references></HashMap>