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
Categorie Soggetti
Pediatrics
Journal title
PEDIATRICS INTERNATIONAL
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.