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Antibody development and disease severity of COVID-19 in non-immunised patients with rheumatic immune-mediated inflammatory diseases: data from a prospective cohort study
BackgroundResearch on the disease severity of COVID-19 in patients with rheumatic immune-mediated inflammatory diseases (IMIDs) has been inconclusive, and long-term prospective data on the development of SARS-CoV-2 antibodies in these patients are lacking.MethodsAdult patients with rheumatic IMIDs f...
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Published in: | Rheumatic & musculoskeletal diseases open 2022-04, Vol.8 (1), p.e002035 |
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creator | Boekel, Laura Hooijberg, Femke Vogelzang, Erik H Besten, Yaëlle R Leeuw, Maureen Atiqi, Sadaf van Vollenhoven, Ronald F Wijbrandts, Carla A Gerritsen, Martijn Krieckaert, C Dijkshoorn, Bas Bakhlakh, Siham Crooijmans, Juliette J Voskuyl, Alexandre van der Horst-Bruinsma, Irene E Lems, Willem Kuijpers, Taco W van Ham, S Marieke Wieske, Luuk Eftimov, Filip Kummer, Laura Y van Dam, PJ Koos Stalman, Eileen W Steenhuis, Maurice Keijzer, Sofie Cristianawati, Olvi Keijser, Jim Loeff, Floris C Tas, Sander W Nurmohamed, Michael T Boers, Maarten Rispens, Theo Wolbink, Gertjan |
description | BackgroundResearch on the disease severity of COVID-19 in patients with rheumatic immune-mediated inflammatory diseases (IMIDs) has been inconclusive, and long-term prospective data on the development of SARS-CoV-2 antibodies in these patients are lacking.MethodsAdult patients with rheumatic IMIDs from the Amsterdam Rheumatology and Immunology Center, Amsterdam were invited to participate. All patients were asked to recruit their own sex-matched and age-matched control subject. Clinical data were collected via online questionnaires (at baseline, and after 1–4 and 5–9 months of follow-up). Serum samples were collected twice and analysed for the presence of SARS-CoV-2-specific antibodies. Subsequently, IgG titres were quantified in samples with a positive test result.FindingsIn total, 3080 consecutive patients and 1102 controls with comparable age and sex distribution were included for analyses. Patients were more frequently hospitalised compared with controls when infected with SARS-CoV-2; 7% vs 0.7% (adjusted OR: 7.33, 95% CI: 0.96 to 55.77). Only treatment with B-cell targeting therapy was independently associated with an increased risk of COVID-19-related hospitalisation (adjusted OR: 14.62, 95% CI: 2.31 to 92.39). IgG antibody titres were higher in hospitalised compared with non-hospitalised patients, and slowly declined with time in similar patterns for patients in all treatment subgroups and controls.InterpretationWe observed that patients with rheumatic IMIDs, especially those treated with B-cell targeting therapy, were more likely to be hospitalised when infected with SARS-CoV-2. Treatment with conventional synthetic disease-modifying antirheumatic drugs (DMARDs) and biological DMARDs other than B-cell targeting agents is unlikely to have negative effects on the development of long-lasting humoral immunity against SARS-CoV-2. |
doi_str_mv | 10.1136/rmdopen-2021-002035 |
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All patients were asked to recruit their own sex-matched and age-matched control subject. Clinical data were collected via online questionnaires (at baseline, and after 1–4 and 5–9 months of follow-up). Serum samples were collected twice and analysed for the presence of SARS-CoV-2-specific antibodies. Subsequently, IgG titres were quantified in samples with a positive test result.FindingsIn total, 3080 consecutive patients and 1102 controls with comparable age and sex distribution were included for analyses. Patients were more frequently hospitalised compared with controls when infected with SARS-CoV-2; 7% vs 0.7% (adjusted OR: 7.33, 95% CI: 0.96 to 55.77). Only treatment with B-cell targeting therapy was independently associated with an increased risk of COVID-19-related hospitalisation (adjusted OR: 14.62, 95% CI: 2.31 to 92.39). IgG antibody titres were higher in hospitalised compared with non-hospitalised patients, and slowly declined with time in similar patterns for patients in all treatment subgroups and controls.InterpretationWe observed that patients with rheumatic IMIDs, especially those treated with B-cell targeting therapy, were more likely to be hospitalised when infected with SARS-CoV-2. Treatment with conventional synthetic disease-modifying antirheumatic drugs (DMARDs) and biological DMARDs other than B-cell targeting agents is unlikely to have negative effects on the development of long-lasting humoral immunity against SARS-CoV-2.</description><identifier>ISSN: 2056-5933</identifier><identifier>EISSN: 2056-5933</identifier><identifier>DOI: 10.1136/rmdopen-2021-002035</identifier><identifier>PMID: 35383121</identifier><language>eng</language><publisher>England: EULAR</publisher><subject>Adult ; Antibodies ; antirheumatic agents ; autoimmune diseases ; biological therapy ; Cohort analysis ; Coronaviruses ; COVID-19 ; COVID-19 - epidemiology ; COVID-19 vaccines ; Disease prevention ; Drugs ; Dyspnea ; epidemiology ; Hospitalization ; Humans ; Immunosuppressive agents ; Infections ; Inflammatory diseases ; Medical research ; Pandemics ; Patients ; Prospective Studies ; Questionnaires ; Research centers ; Rheumatic diseases ; Rheumatic Diseases - complications ; Rheumatoid arthritis ; SARS-CoV-2 ; Severe acute respiratory syndrome coronavirus 2 ; Severity of Illness Index ; Tumor necrosis factor-TNF</subject><ispartof>Rheumatic & musculoskeletal diseases open, 2022-04, Vol.8 (1), p.e002035</ispartof><rights>Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2022 Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ . Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. 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Published by BMJ. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b539t-d5f14566c039d4ea35f93be4defac73cefe7625a8bdbeec6866ea2915d126bd63</citedby><cites>FETCH-LOGICAL-b539t-d5f14566c039d4ea35f93be4defac73cefe7625a8bdbeec6866ea2915d126bd63</cites><orcidid>0000-0002-6274-1934 ; 0000-0001-6591-7838 ; 0000-0001-5473-7786 ; 0000-0002-6885-3953 ; 0000-0001-6438-8663 ; 0000-0002-6969-283X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2647394774/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2647394774?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,38516,43895,44590,53791,53793,55350,74412,75126,77660,77686</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35383121$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boekel, Laura</creatorcontrib><creatorcontrib>Hooijberg, Femke</creatorcontrib><creatorcontrib>Vogelzang, Erik H</creatorcontrib><creatorcontrib>Besten, Yaëlle R</creatorcontrib><creatorcontrib>Leeuw, Maureen</creatorcontrib><creatorcontrib>Atiqi, Sadaf</creatorcontrib><creatorcontrib>van Vollenhoven, Ronald F</creatorcontrib><creatorcontrib>Wijbrandts, Carla A</creatorcontrib><creatorcontrib>Gerritsen, Martijn</creatorcontrib><creatorcontrib>Krieckaert, C</creatorcontrib><creatorcontrib>Dijkshoorn, Bas</creatorcontrib><creatorcontrib>Bakhlakh, Siham</creatorcontrib><creatorcontrib>Crooijmans, Juliette J</creatorcontrib><creatorcontrib>Voskuyl, Alexandre</creatorcontrib><creatorcontrib>van der Horst-Bruinsma, Irene E</creatorcontrib><creatorcontrib>Lems, Willem</creatorcontrib><creatorcontrib>Kuijpers, Taco W</creatorcontrib><creatorcontrib>van Ham, S Marieke</creatorcontrib><creatorcontrib>Wieske, Luuk</creatorcontrib><creatorcontrib>Eftimov, Filip</creatorcontrib><creatorcontrib>Kummer, Laura Y</creatorcontrib><creatorcontrib>van Dam, PJ Koos</creatorcontrib><creatorcontrib>Stalman, Eileen W</creatorcontrib><creatorcontrib>Steenhuis, Maurice</creatorcontrib><creatorcontrib>Keijzer, Sofie</creatorcontrib><creatorcontrib>Cristianawati, Olvi</creatorcontrib><creatorcontrib>Keijser, Jim</creatorcontrib><creatorcontrib>Loeff, Floris C</creatorcontrib><creatorcontrib>Tas, Sander W</creatorcontrib><creatorcontrib>Nurmohamed, Michael T</creatorcontrib><creatorcontrib>Boers, Maarten</creatorcontrib><creatorcontrib>Rispens, Theo</creatorcontrib><creatorcontrib>Wolbink, Gertjan</creatorcontrib><title>Antibody development and disease severity of COVID-19 in non-immunised patients with rheumatic immune-mediated inflammatory diseases: data from a prospective cohort study</title><title>Rheumatic & musculoskeletal diseases open</title><addtitle>RMD Open</addtitle><addtitle>RMD Open</addtitle><description>BackgroundResearch on the disease severity of COVID-19 in patients with rheumatic immune-mediated inflammatory diseases (IMIDs) has been inconclusive, and long-term prospective data on the development of SARS-CoV-2 antibodies in these patients are lacking.MethodsAdult patients with rheumatic IMIDs from the Amsterdam Rheumatology and Immunology Center, Amsterdam were invited to participate. All patients were asked to recruit their own sex-matched and age-matched control subject. Clinical data were collected via online questionnaires (at baseline, and after 1–4 and 5–9 months of follow-up). Serum samples were collected twice and analysed for the presence of SARS-CoV-2-specific antibodies. Subsequently, IgG titres were quantified in samples with a positive test result.FindingsIn total, 3080 consecutive patients and 1102 controls with comparable age and sex distribution were included for analyses. Patients were more frequently hospitalised compared with controls when infected with SARS-CoV-2; 7% vs 0.7% (adjusted OR: 7.33, 95% CI: 0.96 to 55.77). Only treatment with B-cell targeting therapy was independently associated with an increased risk of COVID-19-related hospitalisation (adjusted OR: 14.62, 95% CI: 2.31 to 92.39). IgG antibody titres were higher in hospitalised compared with non-hospitalised patients, and slowly declined with time in similar patterns for patients in all treatment subgroups and controls.InterpretationWe observed that patients with rheumatic IMIDs, especially those treated with B-cell targeting therapy, were more likely to be hospitalised when infected with SARS-CoV-2. Treatment with conventional synthetic disease-modifying antirheumatic drugs (DMARDs) and biological DMARDs other than B-cell targeting agents is unlikely to have negative effects on the development of long-lasting humoral immunity against SARS-CoV-2.</description><subject>Adult</subject><subject>Antibodies</subject><subject>antirheumatic agents</subject><subject>autoimmune diseases</subject><subject>biological therapy</subject><subject>Cohort analysis</subject><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - epidemiology</subject><subject>COVID-19 vaccines</subject><subject>Disease prevention</subject><subject>Drugs</subject><subject>Dyspnea</subject><subject>epidemiology</subject><subject>Hospitalization</subject><subject>Humans</subject><subject>Immunosuppressive agents</subject><subject>Infections</subject><subject>Inflammatory diseases</subject><subject>Medical research</subject><subject>Pandemics</subject><subject>Patients</subject><subject>Prospective Studies</subject><subject>Questionnaires</subject><subject>Research centers</subject><subject>Rheumatic diseases</subject><subject>Rheumatic Diseases - complications</subject><subject>Rheumatoid arthritis</subject><subject>SARS-CoV-2</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Severity of Illness Index</subject><subject>Tumor necrosis factor-TNF</subject><issn>2056-5933</issn><issn>2056-5933</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>9YT</sourceid><sourceid>COVID</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9ks1u1DAUhSMEolXpEyAhS2zYpPVP7CQskKqBwkiVugG2lmPfdDxK7GA7U80r8ZR4flpaFqxs3fvdc-yrUxRvCb4ghInLMBo_gSsppqTEmGLGXxSnFHNR8paxl0_uJ8V5jGuMMakYqwl7XZwwzhpGKDktfl-5ZDtvtsjABgY_jeASUs4gYyOoCCjmerBpi3yPFrc_l59L0iLrkPOutOM4u8wZNKlk82RE9zatUFjBPOaKRnsCyhGMVSlz1vWDGnPPh-2DRfyIjEoK9cGPSKEp-DiBTnYDSPuVDwnFNJvtm-JVr4YI58fzrPhx_eX74lt5c_t1ubi6KTvO2lQa3pOKC6Exa00FivG-ZR1UBnqla6ahh1pQrprOdABaNEKAoi3hhlDRGcHOiuVB13i1llOwowpb6ZWV-4IPd1KF_LcBpGYki9C2ZYpmT9VV1GiWjWusGmLarPXpoDXNXd6BzisKangm-rzj7Ere-Y1s2oZVhGaBD0eB4H_NEJMcbdQwDMqBn6OkoqoFF7zZeb3_B137Obi8qj3F2qquq0yxA6XzmmOA_vExBMtdtOQxWnIXLXmIVp569_QfjzMPQcrA5QHoxvVf3_9J_gFO9N-X</recordid><startdate>20220401</startdate><enddate>20220401</enddate><creator>Boekel, Laura</creator><creator>Hooijberg, Femke</creator><creator>Vogelzang, Erik H</creator><creator>Besten, Yaëlle R</creator><creator>Leeuw, Maureen</creator><creator>Atiqi, Sadaf</creator><creator>van Vollenhoven, Ronald F</creator><creator>Wijbrandts, Carla A</creator><creator>Gerritsen, Martijn</creator><creator>Krieckaert, C</creator><creator>Dijkshoorn, Bas</creator><creator>Bakhlakh, Siham</creator><creator>Crooijmans, Juliette J</creator><creator>Voskuyl, Alexandre</creator><creator>van der Horst-Bruinsma, Irene E</creator><creator>Lems, Willem</creator><creator>Kuijpers, Taco W</creator><creator>van Ham, S Marieke</creator><creator>Wieske, Luuk</creator><creator>Eftimov, Filip</creator><creator>Kummer, Laura Y</creator><creator>van Dam, PJ Koos</creator><creator>Stalman, Eileen W</creator><creator>Steenhuis, Maurice</creator><creator>Keijzer, Sofie</creator><creator>Cristianawati, Olvi</creator><creator>Keijser, Jim</creator><creator>Loeff, Floris C</creator><creator>Tas, Sander W</creator><creator>Nurmohamed, Michael T</creator><creator>Boers, Maarten</creator><creator>Rispens, Theo</creator><creator>Wolbink, Gertjan</creator><general>EULAR</general><general>BMJ Publishing Group LTD</general><general>BMJ Publishing Group</general><scope>9YT</scope><scope>ACMMV</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-6274-1934</orcidid><orcidid>https://orcid.org/0000-0001-6591-7838</orcidid><orcidid>https://orcid.org/0000-0001-5473-7786</orcidid><orcidid>https://orcid.org/0000-0002-6885-3953</orcidid><orcidid>https://orcid.org/0000-0001-6438-8663</orcidid><orcidid>https://orcid.org/0000-0002-6969-283X</orcidid></search><sort><creationdate>20220401</creationdate><title>Antibody development and disease severity of COVID-19 in non-immunised patients with rheumatic immune-mediated inflammatory diseases: data from a prospective cohort study</title><author>Boekel, Laura ; Hooijberg, Femke ; Vogelzang, Erik H ; Besten, Yaëlle R ; Leeuw, Maureen ; Atiqi, Sadaf ; van Vollenhoven, Ronald F ; Wijbrandts, Carla A ; Gerritsen, Martijn ; Krieckaert, C ; Dijkshoorn, Bas ; Bakhlakh, Siham ; Crooijmans, Juliette J ; Voskuyl, Alexandre ; van der Horst-Bruinsma, Irene E ; Lems, Willem ; Kuijpers, Taco W ; van Ham, S Marieke ; Wieske, Luuk ; Eftimov, Filip ; Kummer, Laura Y ; van Dam, PJ Koos ; Stalman, Eileen W ; Steenhuis, Maurice ; Keijzer, Sofie ; Cristianawati, Olvi ; Keijser, Jim ; Loeff, Floris C ; Tas, Sander W ; Nurmohamed, Michael T ; Boers, Maarten ; Rispens, Theo ; Wolbink, Gertjan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b539t-d5f14566c039d4ea35f93be4defac73cefe7625a8bdbeec6866ea2915d126bd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>Antibodies</topic><topic>antirheumatic agents</topic><topic>autoimmune diseases</topic><topic>biological therapy</topic><topic>Cohort analysis</topic><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>COVID-19 - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Rheumatic & musculoskeletal diseases open</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boekel, Laura</au><au>Hooijberg, Femke</au><au>Vogelzang, Erik H</au><au>Besten, Yaëlle R</au><au>Leeuw, Maureen</au><au>Atiqi, Sadaf</au><au>van Vollenhoven, Ronald F</au><au>Wijbrandts, Carla A</au><au>Gerritsen, Martijn</au><au>Krieckaert, C</au><au>Dijkshoorn, Bas</au><au>Bakhlakh, Siham</au><au>Crooijmans, Juliette J</au><au>Voskuyl, Alexandre</au><au>van der Horst-Bruinsma, Irene E</au><au>Lems, Willem</au><au>Kuijpers, Taco W</au><au>van Ham, S Marieke</au><au>Wieske, Luuk</au><au>Eftimov, Filip</au><au>Kummer, Laura Y</au><au>van Dam, PJ Koos</au><au>Stalman, Eileen W</au><au>Steenhuis, Maurice</au><au>Keijzer, Sofie</au><au>Cristianawati, Olvi</au><au>Keijser, Jim</au><au>Loeff, Floris C</au><au>Tas, Sander W</au><au>Nurmohamed, Michael T</au><au>Boers, Maarten</au><au>Rispens, Theo</au><au>Wolbink, Gertjan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibody development and disease severity of COVID-19 in non-immunised patients with rheumatic immune-mediated inflammatory diseases: data from a prospective cohort study</atitle><jtitle>Rheumatic & musculoskeletal diseases open</jtitle><stitle>RMD Open</stitle><addtitle>RMD Open</addtitle><date>2022-04-01</date><risdate>2022</risdate><volume>8</volume><issue>1</issue><spage>e002035</spage><pages>e002035-</pages><issn>2056-5933</issn><eissn>2056-5933</eissn><abstract>BackgroundResearch on the disease severity of COVID-19 in patients with rheumatic immune-mediated inflammatory diseases (IMIDs) has been inconclusive, and long-term prospective data on the development of SARS-CoV-2 antibodies in these patients are lacking.MethodsAdult patients with rheumatic IMIDs from the Amsterdam Rheumatology and Immunology Center, Amsterdam were invited to participate. All patients were asked to recruit their own sex-matched and age-matched control subject. Clinical data were collected via online questionnaires (at baseline, and after 1–4 and 5–9 months of follow-up). Serum samples were collected twice and analysed for the presence of SARS-CoV-2-specific antibodies. Subsequently, IgG titres were quantified in samples with a positive test result.FindingsIn total, 3080 consecutive patients and 1102 controls with comparable age and sex distribution were included for analyses. Patients were more frequently hospitalised compared with controls when infected with SARS-CoV-2; 7% vs 0.7% (adjusted OR: 7.33, 95% CI: 0.96 to 55.77). Only treatment with B-cell targeting therapy was independently associated with an increased risk of COVID-19-related hospitalisation (adjusted OR: 14.62, 95% CI: 2.31 to 92.39). IgG antibody titres were higher in hospitalised compared with non-hospitalised patients, and slowly declined with time in similar patterns for patients in all treatment subgroups and controls.InterpretationWe observed that patients with rheumatic IMIDs, especially those treated with B-cell targeting therapy, were more likely to be hospitalised when infected with SARS-CoV-2. Treatment with conventional synthetic disease-modifying antirheumatic drugs (DMARDs) and biological DMARDs other than B-cell targeting agents is unlikely to have negative effects on the development of long-lasting humoral immunity against SARS-CoV-2.</abstract><cop>England</cop><pub>EULAR</pub><pmid>35383121</pmid><doi>10.1136/rmdopen-2021-002035</doi><orcidid>https://orcid.org/0000-0002-6274-1934</orcidid><orcidid>https://orcid.org/0000-0001-6591-7838</orcidid><orcidid>https://orcid.org/0000-0001-5473-7786</orcidid><orcidid>https://orcid.org/0000-0002-6885-3953</orcidid><orcidid>https://orcid.org/0000-0001-6438-8663</orcidid><orcidid>https://orcid.org/0000-0002-6969-283X</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2056-5933 |
ispartof | Rheumatic & musculoskeletal diseases open, 2022-04, Vol.8 (1), p.e002035 |
issn | 2056-5933 2056-5933 |
language | eng |
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source | BMJ Open Access Journals; Publicly Available Content Database; PubMed Central; Coronavirus Research Database |
subjects | Adult Antibodies antirheumatic agents autoimmune diseases biological therapy Cohort analysis Coronaviruses COVID-19 COVID-19 - epidemiology COVID-19 vaccines Disease prevention Drugs Dyspnea epidemiology Hospitalization Humans Immunosuppressive agents Infections Inflammatory diseases Medical research Pandemics Patients Prospective Studies Questionnaires Research centers Rheumatic diseases Rheumatic Diseases - complications Rheumatoid arthritis SARS-CoV-2 Severe acute respiratory syndrome coronavirus 2 Severity of Illness Index Tumor necrosis factor-TNF |
title | Antibody development and disease severity of COVID-19 in non-immunised patients with rheumatic immune-mediated inflammatory diseases: data from a prospective cohort study |
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