Immunoglobulin allotypic markers in Kawasaki disease

Stanford T. Shulman*, Marian Melish, Osmu Inoue, Hirohisa Kato, Shobun Tomita

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

23 Scopus citations


We investigated the possible relationship of the distribution of immunoglobulin allotypic markers for susceptibility to Kawasaki disease in Japanese, Japanese-American, and white American populations. The kappa-chain allotype Km1 was present in 25.6% of sera from white patients with Kawasaki disease and in 14.4% of control sera (p<0.01), and the combination of Km1 with Gm heterozygosity was present in 17.9% of white patients with Kawasaki disease and in 6.4% of control sera (p<0.0001). In all populations studied, differences were observed between the patients with Kawasaki disease and the race-matched control subjects. The findings support the hypothesis that one or more unknown infectious agents may trigger genetically influenced immune responses that result in clinically recognizable Kawasaki disease.

Original languageEnglish (US)
Pages (from-to)84-86
Number of pages3
JournalThe Journal of pediatrics
Issue number1
StatePublished - Jan 1993

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health


Dive into the research topics of 'Immunoglobulin allotypic markers in Kawasaki disease'. Together they form a unique fingerprint.

Cite this