A framework for understanding Kawasaki disease pathogenesis

Clin Immunol. 2020 May:214:108385. doi: 10.1016/j.clim.2020.108385. Epub 2020 Mar 12.

Abstract

Kawasaki disease (KD) is a common vasculitis of childhood, typically affecting children under the age of five. Despite many aspects of its presentation that bear resemblence to acute infection, no causative infectious agent has been identified despite years of intense scrutiny. Unlike most infections, however, there are significant differences in racial predilection that suggest a strong genetic influence. The inflammatory response in KD specifically targets the coronary arteries, also unusual for an infectious condition. In this review, we discuss recent hypotheses on KD pathogenesis as well as new insights into the innate immune response and mechanisms behind vascular damage. The pathogenesis is complex, however, and remains inadequately understood.

Keywords: IL-1; IgA; Inflammasome; Kawasaki disease; Vasculitis.

Publication types

  • Review

MeSH terms

  • Adaptive Immunity
  • Animals
  • Child, Preschool
  • Cluster Analysis
  • Coronary Vessels / immunology
  • Coronary Vessels / pathology
  • Disease Models, Animal
  • Environmental Exposure
  • Ethnicity / genetics
  • Genetic Predisposition to Disease
  • Genome-Wide Association Study
  • Humans
  • Immunity, Innate
  • Immunoglobulin A / immunology
  • Incidence
  • Infant
  • Infections / complications
  • Inflammation
  • Matrix Metalloproteinases / physiology
  • Mice
  • Mucocutaneous Lymph Node Syndrome / epidemiology
  • Mucocutaneous Lymph Node Syndrome / etiology*
  • Mucocutaneous Lymph Node Syndrome / genetics
  • Mucocutaneous Lymph Node Syndrome / immunology
  • Myocardium / immunology
  • Myocardium / pathology
  • Protease Inhibitors / therapeutic use
  • Racial Groups / genetics

Substances

  • Immunoglobulin A
  • Protease Inhibitors
  • Matrix Metalloproteinases