Analysis of tumor necrosis factor-alpha production and polymorphisms of the tumor necrosis factor-alpha gene in individuals with a history of Kawasaki disease

Citation
S. Kamizono et al., Analysis of tumor necrosis factor-alpha production and polymorphisms of the tumor necrosis factor-alpha gene in individuals with a history of Kawasaki disease, PEDIATR INT, 41(4), 1999, pp. 341-345
Citations number
30
Categorie Soggetti
Pediatrics
Journal title
PEDIATRICS INTERNATIONAL
ISSN journal
13288067 → ACNP
Volume
41
Issue
4
Year of publication
1999
Pages
341 - 345
Database
ISI
SICI code
1328-8067(199908)41:4<341:AOTNFP>2.0.ZU;2-X
Abstract
Background: Tumor necrosis factor (TNF)-alpha plays a central role in the p athogenesis of vasculitis in Kawasaki disease (KD). To address the genetic background of KD, we investigated the level of TNF-alpha production and gen etic polymorphisms in the 5' flanking region of the TNF-alpha gene in healt hy children with a history of KD. Methods: For TNF-alpha production, peripheral blood mononuclear cells (PBMC ) of children with a history of ICD (n = 61) and of non-KD children (n = 35 ) were stimulated with phorbol 12-myristate 13-acetate, toxic shock syndrom e toxin-1 (TSST-1) and the culture supernatant of Staphylococcus aureus der ived from a KD patient (S-6), which had several superantigenic activities. The genetic background of KD was addressed by studying polymorphisms in the 5' flanking region of the TNF-alpha gene at positions - 1031 (thymine (T) to cytosine (C) change, termed - 1031C), - 863 (C to adenine (A), - 863A). - 857 (C to T, - 857T), - 308 (guanine (G) to A, - 308A) and - 238 (G to A, - 238A) in KD, using dot-blot hybridization with sequence-specific oligonu cleotide probes. Results: The PBMC of KD patients with coronary artery lesions produced slig htly higher levels of TNF-alpha in response to the bacterial products (such as TSST-1 and S-6). None of the polymorphisms in the 5' flanking region of the TNF-alpha gene were related to KD. Conclusions: These results suggest that a genetic disposition towards overp roduction of TNF-alpha in response to bacterial products may be involved in the pathogenesis of KD.