Abstract

The aetiology of Kawasaki disease (KD), an acute inflammatory disorder of childhood, remains unknown despite various triggers of KD having been proposed. Host ‘omic profiles offer insights into the host response to infection and inflammation, with the interrogation of multiple ‘omic levels in parallel providing a more comprehensive picture. We used differential abundance analysis, pathway analysis, clustering, and classification techniques to explore whether the host response in KD is more similar to the response to bacterial or viral infections at the transcriptomic and proteomic levels through comparison of ‘omic profiles from children with KD to those with bacterial and viral infections. Pathways activated in patients with KD included those involved in anti-viral and anti-bacterial responses. Unsupervised clustering showed that the majority of KD patients clustered with bacterial patients on both ‘omic levels, whilst application of diagnostic signatures specific for bacterial and viral infections revealed that many transcriptomic KD samples had low probabilities of having bacterial or viral infections, suggesting that KD may be triggered by a different process not typical of either common bacterial or viral infections. Clustering based on the transcriptomic and proteomic responses during KD revealed three clusters of KD patients on both ‘omic levels, suggesting heterogeneity within the inflammatory response during KD. The observed heterogeneity may reflect differences in the host response to a common trigger, or variation dependent on different triggers of the condition.

Highlights

  • Kawasaki disease (KD) is an acute inflammatory disorder first described in Japan over 50 years ago [1]

  • Whole-blood transcriptomic profiles generated from 414 children were included in the analysis, obtained from children with Kawasaki disease (KD; n = 178), confirmed bacterial infection (DB; n = 54), confirmed viral infection (DV; n = 120), and healthy controls (HC; n = 62)

  • We explored whether the host response during KD is more similar to the host response during bacterial or viral infections using transcriptomic and proteomic data

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Summary

Introduction

Kawasaki disease (KD) is an acute inflammatory disorder first described in Japan over 50 years ago [1]. The seasonality and epidemicity seen in areas of high incidence, including Japan, suggest that it is caused by an infectious trigger [7]. The current consensus is that, in some genetically predisposed children, an infectious trigger initiates an abnormal immune response [8,9]. Multiple viral and bacterial pathogens have been suggested as candidates for the trigger, in addition to airborne environmental and fungal triggers [8,10]. Despite the many theories postulated, none have been independently confirmed, and some studies have concluded that KD is likely to be caused by multiple environmental triggers [11]

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