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COVID-19 in Autoinflammatory Diseases with Immunosuppressive Treatment

COVID-19 disease increases interleukin (IL)-1β release. Anti-IL-1-treatment is effective in IL-1-mediated autoinflammatory diseases (AID). This case series presents COVID-19 in patients with IL-1-mediated and unclassified AID with immunosuppressive therapy (IT). Patient 1 is a 34-year-old woman with...

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Autores principales: Welzel, Tatjana, Samba, Samuel Dembi, Klein, Reinhild, van den Anker, Johannes N., Kuemmerle-Deschner, Jasmin B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915607/
https://www.ncbi.nlm.nih.gov/pubmed/33562758
http://dx.doi.org/10.3390/jcm10040605
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author Welzel, Tatjana
Samba, Samuel Dembi
Klein, Reinhild
van den Anker, Johannes N.
Kuemmerle-Deschner, Jasmin B.
author_facet Welzel, Tatjana
Samba, Samuel Dembi
Klein, Reinhild
van den Anker, Johannes N.
Kuemmerle-Deschner, Jasmin B.
author_sort Welzel, Tatjana
collection PubMed
description COVID-19 disease increases interleukin (IL)-1β release. Anti-IL-1-treatment is effective in IL-1-mediated autoinflammatory diseases (AID). This case series presents COVID-19 in patients with IL-1-mediated and unclassified AID with immunosuppressive therapy (IT). Patient 1 is a 34-year-old woman with an unclassified AID and methotrexate. Patients 2 and 3 (14-year-old girl and 12-year-old boy, respectively) have a Cryopyrin-Associated Periodic Syndrome (NLRP3 p.Q703K heterozygous, CAPS) treated with canakinumab 150 mg/month since three and five years, respectively. Patient 4 is a 15-year-old girl who has had familial Mediterranean fever (MEFV p.M694V homozygous) for 3 years treated with canakinumab 150 mg/month and colchicine. All patients had a mild acute COVID-19 course, particularly the adolescent patients. A few weeks after COVID-19 recovery, both CAPS patients developed increased AID activity, necessitating anti-IL-1-treatment intensification in one patient. At day 100, one out of four patients (25%) showed positive antibody response to SARS-CoV-2. This is one of the first reports providing follow-up data about COVID-19 in AID. The risk for severe acute COVID-19 disease was mild/moderate, but increased AID activity post-COVID-19 was detected. Follow-up data and data combination are needed to expand understanding of COVID-19 and SARS-CoV-2 immunity in AID and the role of IT.
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spelling pubmed-79156072021-03-01 COVID-19 in Autoinflammatory Diseases with Immunosuppressive Treatment Welzel, Tatjana Samba, Samuel Dembi Klein, Reinhild van den Anker, Johannes N. Kuemmerle-Deschner, Jasmin B. J Clin Med Article COVID-19 disease increases interleukin (IL)-1β release. Anti-IL-1-treatment is effective in IL-1-mediated autoinflammatory diseases (AID). This case series presents COVID-19 in patients with IL-1-mediated and unclassified AID with immunosuppressive therapy (IT). Patient 1 is a 34-year-old woman with an unclassified AID and methotrexate. Patients 2 and 3 (14-year-old girl and 12-year-old boy, respectively) have a Cryopyrin-Associated Periodic Syndrome (NLRP3 p.Q703K heterozygous, CAPS) treated with canakinumab 150 mg/month since three and five years, respectively. Patient 4 is a 15-year-old girl who has had familial Mediterranean fever (MEFV p.M694V homozygous) for 3 years treated with canakinumab 150 mg/month and colchicine. All patients had a mild acute COVID-19 course, particularly the adolescent patients. A few weeks after COVID-19 recovery, both CAPS patients developed increased AID activity, necessitating anti-IL-1-treatment intensification in one patient. At day 100, one out of four patients (25%) showed positive antibody response to SARS-CoV-2. This is one of the first reports providing follow-up data about COVID-19 in AID. The risk for severe acute COVID-19 disease was mild/moderate, but increased AID activity post-COVID-19 was detected. Follow-up data and data combination are needed to expand understanding of COVID-19 and SARS-CoV-2 immunity in AID and the role of IT. MDPI 2021-02-05 /pmc/articles/PMC7915607/ /pubmed/33562758 http://dx.doi.org/10.3390/jcm10040605 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Welzel, Tatjana
Samba, Samuel Dembi
Klein, Reinhild
van den Anker, Johannes N.
Kuemmerle-Deschner, Jasmin B.
COVID-19 in Autoinflammatory Diseases with Immunosuppressive Treatment
title COVID-19 in Autoinflammatory Diseases with Immunosuppressive Treatment
title_full COVID-19 in Autoinflammatory Diseases with Immunosuppressive Treatment
title_fullStr COVID-19 in Autoinflammatory Diseases with Immunosuppressive Treatment
title_full_unstemmed COVID-19 in Autoinflammatory Diseases with Immunosuppressive Treatment
title_short COVID-19 in Autoinflammatory Diseases with Immunosuppressive Treatment
title_sort covid-19 in autoinflammatory diseases with immunosuppressive treatment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7915607/
https://www.ncbi.nlm.nih.gov/pubmed/33562758
http://dx.doi.org/10.3390/jcm10040605
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