Innate Lymphoid Cells Play a Pathogenic Role in Pericarditis

Summary: We find that cardiac group 2 innate lymphoid cells (ILC2s) are essential for the development of IL-33-induced eosinophilic pericarditis. We show a pathogenic role for ILC2s in cardiac inflammation, in which ILC2s activated by IL-33 drive the development of eosinophilic pericarditis in colla...

Full description

Bibliographic Details
Main Authors: Hee Sun Choi, Taejoon Won, Xuezhou Hou, Guobao Chen, William Bracamonte-Baran, Monica V. Talor, Ivana Jurčová, Ondrej Szárszoi, Lenka Čurnova, Ilja Stříž, Jody E. Hooper, Vojtěch Melenovský, Daniela Čiháková
Format: Article
Language:English
Published: Elsevier 2020-03-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124720302011
id doaj-4d2bebf86a2c4552b5964ddd17e36bc0
record_format Article
spelling doaj-4d2bebf86a2c4552b5964ddd17e36bc02020-11-25T03:01:00ZengElsevierCell Reports2211-12472020-03-0130929893003.e6Innate Lymphoid Cells Play a Pathogenic Role in PericarditisHee Sun Choi0Taejoon Won1Xuezhou Hou2Guobao Chen3William Bracamonte-Baran4Monica V. Talor5Ivana Jurčová6Ondrej Szárszoi7Lenka Čurnova8Ilja Stříž9Jody E. Hooper10Vojtěch Melenovský11Daniela Čiháková12Department of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USADepartment of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USAW. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205, USADepartment of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USADepartment of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USADepartment of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USADepartment of Cardiology, Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech RepublicDepartment of Cardiovascular Surgery, Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech RepublicDepartment of Clinical and Transplant Immunology, Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech RepublicDepartment of Clinical and Transplant Immunology, Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech RepublicDepartment of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USADepartment of Cardiology, Institute for Clinical and Experimental Medicine (IKEM), Prague, Czech RepublicDepartment of Pathology, School of Medicine, Johns Hopkins University, Baltimore, MD 21205, USA; W. Harry Feinstone Department of Molecular Microbiology and Immunology, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205, USA; Corresponding authorSummary: We find that cardiac group 2 innate lymphoid cells (ILC2s) are essential for the development of IL-33-induced eosinophilic pericarditis. We show a pathogenic role for ILC2s in cardiac inflammation, in which ILC2s activated by IL-33 drive the development of eosinophilic pericarditis in collaboration with cardiac fibroblasts. ILCs, not T and B cells, are required for the development of pericarditis. ILC2s transferred to the heart of Rag2−/−Il2rg−/− mice restore their susceptibility to eosinophil infiltration. Moreover, ILC2s direct cardiac fibroblasts to produce eotaxin-1. We also find that eosinophils reside in the mediastinal cavity and that eosinophils transferred to the mediastinal cavity of eosinophil-deficient ΔdblGATA1 mice following IL-33 treatment migrate to the heart. Thus, the serous cavities may serve as a reservoir of cardiac-infiltrating eosinophils. In humans, patients with pericarditis show higher amounts of ILCs in pericardial fluid than do healthy controls and patients with other cardiac diseases. We demonstrate that ILCs play a critical role in pericarditis. : Choi et al. show a pathogenic role for innate lymphoid cells (ILCs) in IL-33-induced eosinophilic pericarditis. ILCs are required for the development of pericarditis, and group 2 ILCs (ILC2s) promote the expression of eotaxin by cardiac fibroblasts. In humans, ILCs are found higher in the pericardial fluid of patients with pericarditis compared to others. Keywords: Innate lymphoid cells, group 2 innate lymphoid cells, IL-33, pericarditis, cardiac inflammation, eosinophils, mediastinum, serosal cavityhttp://www.sciencedirect.com/science/article/pii/S2211124720302011
collection DOAJ
language English
format Article
sources DOAJ
author Hee Sun Choi
Taejoon Won
Xuezhou Hou
Guobao Chen
William Bracamonte-Baran
Monica V. Talor
Ivana Jurčová
Ondrej Szárszoi
Lenka Čurnova
Ilja Stříž
Jody E. Hooper
Vojtěch Melenovský
Daniela Čiháková
spellingShingle Hee Sun Choi
Taejoon Won
Xuezhou Hou
Guobao Chen
William Bracamonte-Baran
Monica V. Talor
Ivana Jurčová
Ondrej Szárszoi
Lenka Čurnova
Ilja Stříž
Jody E. Hooper
Vojtěch Melenovský
Daniela Čiháková
Innate Lymphoid Cells Play a Pathogenic Role in Pericarditis
Cell Reports
author_facet Hee Sun Choi
Taejoon Won
Xuezhou Hou
Guobao Chen
William Bracamonte-Baran
Monica V. Talor
Ivana Jurčová
Ondrej Szárszoi
Lenka Čurnova
Ilja Stříž
Jody E. Hooper
Vojtěch Melenovský
Daniela Čiháková
author_sort Hee Sun Choi
title Innate Lymphoid Cells Play a Pathogenic Role in Pericarditis
title_short Innate Lymphoid Cells Play a Pathogenic Role in Pericarditis
title_full Innate Lymphoid Cells Play a Pathogenic Role in Pericarditis
title_fullStr Innate Lymphoid Cells Play a Pathogenic Role in Pericarditis
title_full_unstemmed Innate Lymphoid Cells Play a Pathogenic Role in Pericarditis
title_sort innate lymphoid cells play a pathogenic role in pericarditis
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2020-03-01
description Summary: We find that cardiac group 2 innate lymphoid cells (ILC2s) are essential for the development of IL-33-induced eosinophilic pericarditis. We show a pathogenic role for ILC2s in cardiac inflammation, in which ILC2s activated by IL-33 drive the development of eosinophilic pericarditis in collaboration with cardiac fibroblasts. ILCs, not T and B cells, are required for the development of pericarditis. ILC2s transferred to the heart of Rag2−/−Il2rg−/− mice restore their susceptibility to eosinophil infiltration. Moreover, ILC2s direct cardiac fibroblasts to produce eotaxin-1. We also find that eosinophils reside in the mediastinal cavity and that eosinophils transferred to the mediastinal cavity of eosinophil-deficient ΔdblGATA1 mice following IL-33 treatment migrate to the heart. Thus, the serous cavities may serve as a reservoir of cardiac-infiltrating eosinophils. In humans, patients with pericarditis show higher amounts of ILCs in pericardial fluid than do healthy controls and patients with other cardiac diseases. We demonstrate that ILCs play a critical role in pericarditis. : Choi et al. show a pathogenic role for innate lymphoid cells (ILCs) in IL-33-induced eosinophilic pericarditis. ILCs are required for the development of pericarditis, and group 2 ILCs (ILC2s) promote the expression of eotaxin by cardiac fibroblasts. In humans, ILCs are found higher in the pericardial fluid of patients with pericarditis compared to others. Keywords: Innate lymphoid cells, group 2 innate lymphoid cells, IL-33, pericarditis, cardiac inflammation, eosinophils, mediastinum, serosal cavity
url http://www.sciencedirect.com/science/article/pii/S2211124720302011
work_keys_str_mv AT heesunchoi innatelymphoidcellsplayapathogenicroleinpericarditis
AT taejoonwon innatelymphoidcellsplayapathogenicroleinpericarditis
AT xuezhouhou innatelymphoidcellsplayapathogenicroleinpericarditis
AT guobaochen innatelymphoidcellsplayapathogenicroleinpericarditis
AT williambracamontebaran innatelymphoidcellsplayapathogenicroleinpericarditis
AT monicavtalor innatelymphoidcellsplayapathogenicroleinpericarditis
AT ivanajurcova innatelymphoidcellsplayapathogenicroleinpericarditis
AT ondrejszarszoi innatelymphoidcellsplayapathogenicroleinpericarditis
AT lenkacurnova innatelymphoidcellsplayapathogenicroleinpericarditis
AT iljastriz innatelymphoidcellsplayapathogenicroleinpericarditis
AT jodyehooper innatelymphoidcellsplayapathogenicroleinpericarditis
AT vojtechmelenovsky innatelymphoidcellsplayapathogenicroleinpericarditis
AT danielacihakova innatelymphoidcellsplayapathogenicroleinpericarditis
_version_ 1724695507685605376