Transcript abundance patterns in Kawasaki disease patients with intravenous immunoglobulin resistance

Hum Immunol. 2010 Sep;71(9):865-73. doi: 10.1016/j.humimm.2010.06.008. Epub 2010 Jun 20.

Abstract

Intravenous immunoglobulin (IVIG)-resistant Kawasaki disease (KD) patients comprise at least 20% of treated patients and are at high risk for coronary artery abnormalities. If identified early in the course of the disease, such patients may benefit from additional anti-inflammatory therapy. The aim of this study was to compare the transcript abundance between IVIG resistant and -responsive KD patients, to identify biomarkers that might differentiate between these two groups and to generate new targets for therapies in IVIG resistant KD patients. We compared the transcript abundance profiles of whole-blood RNA on Agilent arrays from acute and convalescent KD subjects and age-similar, healthy controls. KD subjects were stratified as IVIG resistant or -responsive based on response to initial IVIG therapy. Transcript abundance was higher for IL-1 pathway genes (IL-1 receptor, interleukin receptor associated kinase, p38 mitogen-activated protein kinase), and MMP-8. These findings point to candidate biomarkers that may predict IVIG resistance in acute KD patients. The results also underscore the importance of the IL-1 pathway as a mediator of inflammation in KD and suggest that IL-1 or its receptor may be reasonable targets for therapy, particularly for IVIG resistant patients.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antigens, CD / genetics
  • Biomarkers / blood
  • Cell Adhesion Molecules / genetics
  • Child
  • Child, Preschool
  • Complement C1q / genetics
  • Drug Resistance / genetics*
  • Female
  • GPI-Linked Proteins / genetics
  • Gene Expression / genetics
  • Gene Expression Profiling*
  • Humans
  • Immunoglobulins, Intravenous / therapeutic use*
  • Infant
  • Interleukin-1 / metabolism
  • Interleukin-1 Receptor-Associated Kinases / genetics
  • Male
  • Matrix Metalloproteinase 8 / blood
  • Matrix Metalloproteinase 8 / genetics
  • Mucocutaneous Lymph Node Syndrome / blood
  • Mucocutaneous Lymph Node Syndrome / drug therapy*
  • Mucocutaneous Lymph Node Syndrome / genetics*
  • NF-kappa B / genetics
  • Oligonucleotide Array Sequence Analysis
  • RNA, Messenger / analysis*
  • RNA, Messenger / genetics
  • Receptors, Interleukin-1 Type II / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • S100 Proteins / genetics
  • Signal Transduction / genetics
  • Transcription, Genetic / genetics*
  • Up-Regulation / genetics

Substances

  • Antigens, CD
  • Biomarkers
  • CD66 antigens
  • CEACAM8 protein, human
  • Cell Adhesion Molecules
  • GPI-Linked Proteins
  • IL1R2 protein, human
  • Immunoglobulins, Intravenous
  • Interleukin-1
  • NF-kappa B
  • RNA, Messenger
  • Receptors, Interleukin-1 Type II
  • S100 Proteins
  • Complement C1q
  • Interleukin-1 Receptor-Associated Kinases
  • Matrix Metalloproteinase 8