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Recurrent Pericarditis: a Stubborn Opponent Meets New Treatments in 2022

PURPOSE OF REVIEW: Our goal in writing this review was to provide a comprehensive appraisal of current therapies for idiopathic recurrent pericarditis with a particular focus on the newest therapeutic agents. We sought to understand the role of the inflammasome in the pathophysiology of pericarditis...

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Autores principales: Hagerty, Tracy, Kluge, Matthew A., LeWinter, Martin M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130990/
https://www.ncbi.nlm.nih.gov/pubmed/35612721
http://dx.doi.org/10.1007/s11886-022-01719-z
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author Hagerty, Tracy
Kluge, Matthew A.
LeWinter, Martin M.
author_facet Hagerty, Tracy
Kluge, Matthew A.
LeWinter, Martin M.
author_sort Hagerty, Tracy
collection PubMed
description PURPOSE OF REVIEW: Our goal in writing this review was to provide a comprehensive appraisal of current therapies for idiopathic recurrent pericarditis with a particular focus on the newest therapeutic agents. We sought to understand the role of the inflammasome in the pathophysiology of pericarditis and how it informs the use of interleukin-1 (IL-1)-directed therapies. RECENT FINDINGS: The latest research on this topic has focused on the critical role of the NLRP3 (NACHT, leucine-rich repeat, and pyrin domain-containing protein) inflammasome. Very recently, components of the NLRP3 inflammasome were detected by immune staining in pericardial tissue from patients with recurrent idiopathic pericarditis. In a mouse model of pericarditis, anti-IL-1 agents anakinra and rilonacept reduced NLRP3 immunostaining. Subsequent study of these drugs in human subjects with idiopathic recurrent pericarditis demonstrated their efficacy. SUMMARY: Recurrent idiopathic pericarditis, while relatively rare, poses a continued treatment challenge and contributes to a diminished quality of life for those patients who are afflicted. Recent developments, including an animal model of the disease and the use of IL-1-directed therapies, represent an exciting leap forward in our understanding of treatment targets. These advances offer not only new tools in our fight against this disease, but also the promise of earlier intervention and attenuation of disease morbidity. As our experience with these new agents expands, we can address questions about the ideal timing of introduction of anti-IL-1 therapy and duration of therapy and better understand the potential side effect profile. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11886-022-01719-z.
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spelling pubmed-91309902022-05-25 Recurrent Pericarditis: a Stubborn Opponent Meets New Treatments in 2022 Hagerty, Tracy Kluge, Matthew A. LeWinter, Martin M. Curr Cardiol Rep Pericardial Disease (AL Klein and CL Jellis, Section Editors) PURPOSE OF REVIEW: Our goal in writing this review was to provide a comprehensive appraisal of current therapies for idiopathic recurrent pericarditis with a particular focus on the newest therapeutic agents. We sought to understand the role of the inflammasome in the pathophysiology of pericarditis and how it informs the use of interleukin-1 (IL-1)-directed therapies. RECENT FINDINGS: The latest research on this topic has focused on the critical role of the NLRP3 (NACHT, leucine-rich repeat, and pyrin domain-containing protein) inflammasome. Very recently, components of the NLRP3 inflammasome were detected by immune staining in pericardial tissue from patients with recurrent idiopathic pericarditis. In a mouse model of pericarditis, anti-IL-1 agents anakinra and rilonacept reduced NLRP3 immunostaining. Subsequent study of these drugs in human subjects with idiopathic recurrent pericarditis demonstrated their efficacy. SUMMARY: Recurrent idiopathic pericarditis, while relatively rare, poses a continued treatment challenge and contributes to a diminished quality of life for those patients who are afflicted. Recent developments, including an animal model of the disease and the use of IL-1-directed therapies, represent an exciting leap forward in our understanding of treatment targets. These advances offer not only new tools in our fight against this disease, but also the promise of earlier intervention and attenuation of disease morbidity. As our experience with these new agents expands, we can address questions about the ideal timing of introduction of anti-IL-1 therapy and duration of therapy and better understand the potential side effect profile. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11886-022-01719-z. Springer US 2022-05-25 2022 /pmc/articles/PMC9130990/ /pubmed/35612721 http://dx.doi.org/10.1007/s11886-022-01719-z Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Pericardial Disease (AL Klein and CL Jellis, Section Editors)
Hagerty, Tracy
Kluge, Matthew A.
LeWinter, Martin M.
Recurrent Pericarditis: a Stubborn Opponent Meets New Treatments in 2022
title Recurrent Pericarditis: a Stubborn Opponent Meets New Treatments in 2022
title_full Recurrent Pericarditis: a Stubborn Opponent Meets New Treatments in 2022
title_fullStr Recurrent Pericarditis: a Stubborn Opponent Meets New Treatments in 2022
title_full_unstemmed Recurrent Pericarditis: a Stubborn Opponent Meets New Treatments in 2022
title_short Recurrent Pericarditis: a Stubborn Opponent Meets New Treatments in 2022
title_sort recurrent pericarditis: a stubborn opponent meets new treatments in 2022
topic Pericardial Disease (AL Klein and CL Jellis, Section Editors)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130990/
https://www.ncbi.nlm.nih.gov/pubmed/35612721
http://dx.doi.org/10.1007/s11886-022-01719-z
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