Impact of Immunotherapies on SARS-CoV-2-Infections and Other Respiratory Tract Infections during the COVID-19 Winter Season in IBD Patients
Background. COVID-19 represents one of the most significant medical problems of our time. Aims. This study is focused on the question whether patients with inflammatory bowel disease (IBD) who receive immunotherapies are more vulnerable to respiratory tract infections and SARS-CoV-2 infections in co...
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creator | Waggershauser, Constanze Heike Tillack-Schreiber, Cornelia Weyh, Paul Alt, Eckard Siegmund, Thorsten Berchthold-Benchieb, Christine Szokodi, Daniel Schnitzler, Fabian Ochsenkühn, Thomas |
description | Background. COVID-19 represents one of the most significant medical problems of our time. Aims. This study is focused on the question whether patients with inflammatory bowel disease (IBD) who receive immunotherapies are more vulnerable to respiratory tract infections and SARS-CoV-2 infections in comparison to medical staff, as a cohort with an increased infection risk, and to the general population in a COVID-19 hotspot. Methods. We analysed data regarding respiratory tract infections that were collected in our IBD registry and compared them with corresponding data from medical employees in our associated Isarklinikum hospital and from the healthy general population in Munich, Germany, over the same time frame in April and June 2020. Patients were tested for SARS-CoV-2 immunoglobulins (Ig). Results. Symptoms of respiratory tract infections occurred equally frequent in IBD patients with immunotherapies as compared to those without. Older age (>49 years), TNF-inhibitor, and ustekinumab treatment showed a significantly protective role in preventing respiratory tract symptomatic COVID-19 infections that occurred in 0.45% of all our 1.091 IBD patients. Of those, 1.8% were positive for SARS-CoV-2 Ig, identically to the general population of Munich with also 1.8% positivity. Whilst more than 3% of all COVID-19 subjects of the general population died during the first wave, none of our IBD patients died or needed referral to the ICU or oxygen treatment. Conclusions. In our study, IBD patients are as susceptible to respiratory tract infections or SARS-CoV-2 as the normal population. There is no evidence of an association between IBD therapies and increased risk of COVID-19. Interestingly, a reduced rate of COVID-19 deaths in IBD patients, the majority on immunomodulator therapy, was observed, compared to the general population. Therefore, no evidence was found to suggest that IBD medication should be withheld, and adherence should be encouraged to prevent flares. In addition to older age (>49 years), TNF inhibitors and ustekinumab show a protective role in preventing respiratory tract infections. In addition, these results add to the growing evidence that supports further investigation of TNF inhibitors as a possible treatment in the early course of severe COVID-19. |
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COVID-19 represents one of the most significant medical problems of our time. Aims. This study is focused on the question whether patients with inflammatory bowel disease (IBD) who receive immunotherapies are more vulnerable to respiratory tract infections and SARS-CoV-2 infections in comparison to medical staff, as a cohort with an increased infection risk, and to the general population in a COVID-19 hotspot. Methods. We analysed data regarding respiratory tract infections that were collected in our IBD registry and compared them with corresponding data from medical employees in our associated Isarklinikum hospital and from the healthy general population in Munich, Germany, over the same time frame in April and June 2020. Patients were tested for SARS-CoV-2 immunoglobulins (Ig). Results. Symptoms of respiratory tract infections occurred equally frequent in IBD patients with immunotherapies as compared to those without. Older age (>49 years), TNF-inhibitor, and ustekinumab treatment showed a significantly protective role in preventing respiratory tract symptomatic COVID-19 infections that occurred in 0.45% of all our 1.091 IBD patients. Of those, 1.8% were positive for SARS-CoV-2 Ig, identically to the general population of Munich with also 1.8% positivity. Whilst more than 3% of all COVID-19 subjects of the general population died during the first wave, none of our IBD patients died or needed referral to the ICU or oxygen treatment. Conclusions. In our study, IBD patients are as susceptible to respiratory tract infections or SARS-CoV-2 as the normal population. There is no evidence of an association between IBD therapies and increased risk of COVID-19. Interestingly, a reduced rate of COVID-19 deaths in IBD patients, the majority on immunomodulator therapy, was observed, compared to the general population. Therefore, no evidence was found to suggest that IBD medication should be withheld, and adherence should be encouraged to prevent flares. In addition to older age (>49 years), TNF inhibitors and ustekinumab show a protective role in preventing respiratory tract infections. In addition, these results add to the growing evidence that supports further investigation of TNF inhibitors as a possible treatment in the early course of severe COVID-19.</description><identifier>ISSN: 2291-2789</identifier><identifier>EISSN: 2291-2797</identifier><identifier>DOI: 10.1155/2022/3469789</identifier><identifier>PMID: 36060521</identifier><language>eng</language><publisher>Egypt: Hindawi</publisher><subject>Coronaviruses ; COVID-19 ; COVID-19 - epidemiology ; Humans ; Immunotherapy ; Inflammatory bowel disease ; Inflammatory Bowel Diseases - drug therapy ; Inflammatory Bowel Diseases - therapy ; SARS-CoV-2 ; Seasons ; Severe acute respiratory syndrome coronavirus 2 ; Tumor Necrosis Factor Inhibitors ; Ustekinumab - therapeutic use</subject><ispartof>Canadian Journal of Gastroenterology and Hepatology, 2022, Vol.2022, p.3469789-9</ispartof><rights>Copyright © 2022 Constanze Heike Waggershauser et al.</rights><rights>Copyright © 2022 Constanze Heike Waggershauser et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. https://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2022 Constanze Heike Waggershauser et al. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c471t-6e4e2030e393b4276c2b0c70933be080ecadfac7b222139f31dac9037dfa35103</cites><orcidid>0000-0002-2831-9270 ; 0000-0002-0451-7280 ; 0000-0002-6687-139X ; 0000-0002-3037-0921 ; 0000-0001-8260-8594 ; 0000-0002-9304-5325 ; 0000-0002-8425-1557 ; 0000-0001-6976-3653 ; 0000-0002-9442-3578</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433291/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9433291/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,315,728,781,785,865,878,886,4025,27927,27928,27929,53795,53797</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36060521$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Granito, Alessandro</contributor><contributor>Alessandro Granito</contributor><creatorcontrib>Waggershauser, Constanze Heike</creatorcontrib><creatorcontrib>Tillack-Schreiber, Cornelia</creatorcontrib><creatorcontrib>Weyh, Paul</creatorcontrib><creatorcontrib>Alt, Eckard</creatorcontrib><creatorcontrib>Siegmund, Thorsten</creatorcontrib><creatorcontrib>Berchthold-Benchieb, Christine</creatorcontrib><creatorcontrib>Szokodi, Daniel</creatorcontrib><creatorcontrib>Schnitzler, Fabian</creatorcontrib><creatorcontrib>Ochsenkühn, Thomas</creatorcontrib><title>Impact of Immunotherapies on SARS-CoV-2-Infections and Other Respiratory Tract Infections during the COVID-19 Winter Season in IBD Patients</title><title>Canadian Journal of Gastroenterology and Hepatology</title><addtitle>Can J Gastroenterol Hepatol</addtitle><description>Background. COVID-19 represents one of the most significant medical problems of our time. Aims. This study is focused on the question whether patients with inflammatory bowel disease (IBD) who receive immunotherapies are more vulnerable to respiratory tract infections and SARS-CoV-2 infections in comparison to medical staff, as a cohort with an increased infection risk, and to the general population in a COVID-19 hotspot. Methods. We analysed data regarding respiratory tract infections that were collected in our IBD registry and compared them with corresponding data from medical employees in our associated Isarklinikum hospital and from the healthy general population in Munich, Germany, over the same time frame in April and June 2020. Patients were tested for SARS-CoV-2 immunoglobulins (Ig). Results. Symptoms of respiratory tract infections occurred equally frequent in IBD patients with immunotherapies as compared to those without. Older age (>49 years), TNF-inhibitor, and ustekinumab treatment showed a significantly protective role in preventing respiratory tract symptomatic COVID-19 infections that occurred in 0.45% of all our 1.091 IBD patients. Of those, 1.8% were positive for SARS-CoV-2 Ig, identically to the general population of Munich with also 1.8% positivity. Whilst more than 3% of all COVID-19 subjects of the general population died during the first wave, none of our IBD patients died or needed referral to the ICU or oxygen treatment. Conclusions. In our study, IBD patients are as susceptible to respiratory tract infections or SARS-CoV-2 as the normal population. There is no evidence of an association between IBD therapies and increased risk of COVID-19. Interestingly, a reduced rate of COVID-19 deaths in IBD patients, the majority on immunomodulator therapy, was observed, compared to the general population. Therefore, no evidence was found to suggest that IBD medication should be withheld, and adherence should be encouraged to prevent flares. In addition to older age (>49 years), TNF inhibitors and ustekinumab show a protective role in preventing respiratory tract infections. In addition, these results add to the growing evidence that supports further investigation of TNF inhibitors as a possible treatment in the early course of severe COVID-19.</description><subject>Coronaviruses</subject><subject>COVID-19</subject><subject>COVID-19 - epidemiology</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory Bowel Diseases - drug therapy</subject><subject>Inflammatory Bowel Diseases - therapy</subject><subject>SARS-CoV-2</subject><subject>Seasons</subject><subject>Severe acute respiratory syndrome coronavirus 2</subject><subject>Tumor Necrosis Factor Inhibitors</subject><subject>Ustekinumab - therapeutic use</subject><issn>2291-2789</issn><issn>2291-2797</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>RHX</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>DOA</sourceid><recordid>eNp9kktv1DAQgC1ERavSG2dkiSOk9SOJ1xeksuURqdKibilHy7GdXa82drAdUH8Dfxqnu121F062xt98ntEMAG8wOse4qi4IIuSCljVnM_4CnBDCcUEYZy8P9xk_BmcxbhBCmFQVp-QVOKY1qlFF8An42_SDVAn6DjZ9Pzqf1ibIwZoIvYPLy5tlMfd3BSka1xmVrHcRSqfhYuLgjYmDDTL5cA9vw-R5gukxWLeCGYTzxV1zVWAOf1qXct7SyJj11sHm0xX8LpM1LsXX4KiT22jO9ucp-PHl8-38W3G9-NrML68LVTKcitqUhiCKDOW0LQmrFWmRYohT2ho0Q0ZJ3UnFWkIIpryjWEvFEWU5SiuM6Clodl7t5UYMwfYy3AsvrXgI-LASMiSrtkbI7Mr57eQpK4R5rRXBtUaMzepO6-z6uHMNY9sbrXIfQW6fSZ-_OLsWK_9b8JLSPKEseLcXBP9rNDGJjR-Dy_0LknuaBkankj_sKBV8jMF0hx8wEtMmiGkTxH4TMv72aVUH-HHuGXi_A9bWafnH_l_3D_Rwupg</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Waggershauser, Constanze Heike</creator><creator>Tillack-Schreiber, Cornelia</creator><creator>Weyh, Paul</creator><creator>Alt, Eckard</creator><creator>Siegmund, Thorsten</creator><creator>Berchthold-Benchieb, Christine</creator><creator>Szokodi, Daniel</creator><creator>Schnitzler, Fabian</creator><creator>Ochsenkühn, Thomas</creator><general>Hindawi</general><general>Hindawi Limited</general><scope>RHU</scope><scope>RHW</scope><scope>RHX</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>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8FQ</scope><scope>8FV</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>COVID</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-2831-9270</orcidid><orcidid>https://orcid.org/0000-0002-0451-7280</orcidid><orcidid>https://orcid.org/0000-0002-6687-139X</orcidid><orcidid>https://orcid.org/0000-0002-3037-0921</orcidid><orcidid>https://orcid.org/0000-0001-8260-8594</orcidid><orcidid>https://orcid.org/0000-0002-9304-5325</orcidid><orcidid>https://orcid.org/0000-0002-8425-1557</orcidid><orcidid>https://orcid.org/0000-0001-6976-3653</orcidid><orcidid>https://orcid.org/0000-0002-9442-3578</orcidid></search><sort><creationdate>2022</creationdate><title>Impact of Immunotherapies on SARS-CoV-2-Infections and Other Respiratory Tract Infections during the COVID-19 Winter Season in IBD Patients</title><author>Waggershauser, Constanze Heike ; Tillack-Schreiber, Cornelia ; Weyh, Paul ; Alt, Eckard ; Siegmund, Thorsten ; Berchthold-Benchieb, Christine ; Szokodi, Daniel ; Schnitzler, Fabian ; Ochsenkühn, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-6e4e2030e393b4276c2b0c70933be080ecadfac7b222139f31dac9037dfa35103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Coronaviruses</topic><topic>COVID-19</topic><topic>COVID-19 - epidemiology</topic><topic>Humans</topic><topic>Immunotherapy</topic><topic>Inflammatory bowel disease</topic><topic>Inflammatory Bowel Diseases - drug therapy</topic><topic>Inflammatory Bowel Diseases - therapy</topic><topic>SARS-CoV-2</topic><topic>Seasons</topic><topic>Severe acute respiratory syndrome coronavirus 2</topic><topic>Tumor Necrosis Factor Inhibitors</topic><topic>Ustekinumab - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Waggershauser, Constanze Heike</creatorcontrib><creatorcontrib>Tillack-Schreiber, Cornelia</creatorcontrib><creatorcontrib>Weyh, Paul</creatorcontrib><creatorcontrib>Alt, Eckard</creatorcontrib><creatorcontrib>Siegmund, Thorsten</creatorcontrib><creatorcontrib>Berchthold-Benchieb, Christine</creatorcontrib><creatorcontrib>Szokodi, Daniel</creatorcontrib><creatorcontrib>Schnitzler, Fabian</creatorcontrib><creatorcontrib>Ochsenkühn, Thomas</creatorcontrib><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Canadian Business & Current Affairs Database</collection><collection>Canadian Business & Current Affairs Database (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Coronavirus Research Database</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Canadian Journal of Gastroenterology and Hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Waggershauser, Constanze Heike</au><au>Tillack-Schreiber, Cornelia</au><au>Weyh, Paul</au><au>Alt, Eckard</au><au>Siegmund, Thorsten</au><au>Berchthold-Benchieb, Christine</au><au>Szokodi, Daniel</au><au>Schnitzler, Fabian</au><au>Ochsenkühn, Thomas</au><au>Granito, Alessandro</au><au>Alessandro Granito</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of Immunotherapies on SARS-CoV-2-Infections and Other Respiratory Tract Infections during the COVID-19 Winter Season in IBD Patients</atitle><jtitle>Canadian Journal of Gastroenterology and Hepatology</jtitle><addtitle>Can J Gastroenterol Hepatol</addtitle><date>2022</date><risdate>2022</risdate><volume>2022</volume><spage>3469789</spage><epage>9</epage><pages>3469789-9</pages><issn>2291-2789</issn><eissn>2291-2797</eissn><abstract>Background. COVID-19 represents one of the most significant medical problems of our time. Aims. This study is focused on the question whether patients with inflammatory bowel disease (IBD) who receive immunotherapies are more vulnerable to respiratory tract infections and SARS-CoV-2 infections in comparison to medical staff, as a cohort with an increased infection risk, and to the general population in a COVID-19 hotspot. Methods. We analysed data regarding respiratory tract infections that were collected in our IBD registry and compared them with corresponding data from medical employees in our associated Isarklinikum hospital and from the healthy general population in Munich, Germany, over the same time frame in April and June 2020. Patients were tested for SARS-CoV-2 immunoglobulins (Ig). Results. Symptoms of respiratory tract infections occurred equally frequent in IBD patients with immunotherapies as compared to those without. Older age (>49 years), TNF-inhibitor, and ustekinumab treatment showed a significantly protective role in preventing respiratory tract symptomatic COVID-19 infections that occurred in 0.45% of all our 1.091 IBD patients. Of those, 1.8% were positive for SARS-CoV-2 Ig, identically to the general population of Munich with also 1.8% positivity. Whilst more than 3% of all COVID-19 subjects of the general population died during the first wave, none of our IBD patients died or needed referral to the ICU or oxygen treatment. Conclusions. In our study, IBD patients are as susceptible to respiratory tract infections or SARS-CoV-2 as the normal population. There is no evidence of an association between IBD therapies and increased risk of COVID-19. Interestingly, a reduced rate of COVID-19 deaths in IBD patients, the majority on immunomodulator therapy, was observed, compared to the general population. Therefore, no evidence was found to suggest that IBD medication should be withheld, and adherence should be encouraged to prevent flares. In addition to older age (>49 years), TNF inhibitors and ustekinumab show a protective role in preventing respiratory tract infections. In addition, these results add to the growing evidence that supports further investigation of TNF inhibitors as a possible treatment in the early course of severe COVID-19.</abstract><cop>Egypt</cop><pub>Hindawi</pub><pmid>36060521</pmid><doi>10.1155/2022/3469789</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-2831-9270</orcidid><orcidid>https://orcid.org/0000-0002-0451-7280</orcidid><orcidid>https://orcid.org/0000-0002-6687-139X</orcidid><orcidid>https://orcid.org/0000-0002-3037-0921</orcidid><orcidid>https://orcid.org/0000-0001-8260-8594</orcidid><orcidid>https://orcid.org/0000-0002-9304-5325</orcidid><orcidid>https://orcid.org/0000-0002-8425-1557</orcidid><orcidid>https://orcid.org/0000-0001-6976-3653</orcidid><orcidid>https://orcid.org/0000-0002-9442-3578</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Coronaviruses COVID-19 COVID-19 - epidemiology Humans Immunotherapy Inflammatory bowel disease Inflammatory Bowel Diseases - drug therapy Inflammatory Bowel Diseases - therapy SARS-CoV-2 Seasons Severe acute respiratory syndrome coronavirus 2 Tumor Necrosis Factor Inhibitors Ustekinumab - therapeutic use |
title | Impact of Immunotherapies on SARS-CoV-2-Infections and Other Respiratory Tract Infections during the COVID-19 Winter Season in IBD Patients |
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