How Should We Classify Kawasaki Disease?

The exact classification of Kawasaki disease (KD) has been debated. Infectious disease specialists have claimed it as an infection with a classic immune responses to an as yet unidentified pathogen that localizes to the coronary arteries. Others have favored an autoreactive hypothesis that KD is tri...

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Main Authors: Edoardo Marrani, Jane C. Burns, Rolando Cimaz
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-12-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2018.02974/full
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author Edoardo Marrani
Jane C. Burns
Rolando Cimaz
author_facet Edoardo Marrani
Jane C. Burns
Rolando Cimaz
author_sort Edoardo Marrani
collection DOAJ
description The exact classification of Kawasaki disease (KD) has been debated. Infectious disease specialists have claimed it as an infection with a classic immune responses to an as yet unidentified pathogen that localizes to the coronary arteries. Others have favored an autoreactive hypothesis that KD is triggered by an antigen that shares homology with structures in the vascular wall, and molecular mimicry resulting in an immune response directed to that tissue. Rheumatologists have classified it as a systemic vasculitis, while some immunologists have stressed the robust nature of the innate immune response that causes both systemic inflammation as well as damage to the coronary arterial wall and questioned whether KD falls within the spectrum of autoinflammatory diseases. This review will describe the evidences available up to now regarding these hypotheses.
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spelling doaj.art-895f9cbfdfa04e5e90e6dc5f6973be1b2022-12-21T23:09:07ZengFrontiers Media S.A.Frontiers in Immunology1664-32242018-12-01910.3389/fimmu.2018.02974415759How Should We Classify Kawasaki Disease?Edoardo Marrani0Jane C. Burns1Rolando Cimaz2Rheumatology Unit, Department of Neurosciences, Psychology, Drug Research and Child Health, Meyer Children's Hospital, University of Florence, Florence, ItalyDepartment of Pediatrics, Kawasaki Disease Research Center, Rady Children's Hospital, University of California, San Diego, San Diego, CA, United StatesRheumatology Unit, Department of Neurosciences, Psychology, Drug Research and Child Health, Meyer Children's Hospital, University of Florence, Florence, ItalyThe exact classification of Kawasaki disease (KD) has been debated. Infectious disease specialists have claimed it as an infection with a classic immune responses to an as yet unidentified pathogen that localizes to the coronary arteries. Others have favored an autoreactive hypothesis that KD is triggered by an antigen that shares homology with structures in the vascular wall, and molecular mimicry resulting in an immune response directed to that tissue. Rheumatologists have classified it as a systemic vasculitis, while some immunologists have stressed the robust nature of the innate immune response that causes both systemic inflammation as well as damage to the coronary arterial wall and questioned whether KD falls within the spectrum of autoinflammatory diseases. This review will describe the evidences available up to now regarding these hypotheses.https://www.frontiersin.org/article/10.3389/fimmu.2018.02974/fullKawasaki diseaseetiopathogenesispediatric vasculitisintravenous immune globulin (IVIg)coronary aneurysm
spellingShingle Edoardo Marrani
Jane C. Burns
Rolando Cimaz
How Should We Classify Kawasaki Disease?
Frontiers in Immunology
Kawasaki disease
etiopathogenesis
pediatric vasculitis
intravenous immune globulin (IVIg)
coronary aneurysm
title How Should We Classify Kawasaki Disease?
title_full How Should We Classify Kawasaki Disease?
title_fullStr How Should We Classify Kawasaki Disease?
title_full_unstemmed How Should We Classify Kawasaki Disease?
title_short How Should We Classify Kawasaki Disease?
title_sort how should we classify kawasaki disease
topic Kawasaki disease
etiopathogenesis
pediatric vasculitis
intravenous immune globulin (IVIg)
coronary aneurysm
url https://www.frontiersin.org/article/10.3389/fimmu.2018.02974/full
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