N. Urushihara et al., Elevation of serum interleukin-18 levels and activation of Kupffer cells in biliary atresia, J PED SURG, 35(3), 2000, pp. 446-449
Background/Purpose: Interleukin-18 (IL-18)/interferon-gamma-inducing factor
(IGIF) is a novel proinflammatory cytokine that can induce interferon gamm
a (IFN-gamma). In addition, IL-18 enhances intracellular adhesion molecule-
1 (ICAM-1) expression as well as Fas ligand (FasL) expression, and induces
apoptosis in hepatic injury. The aim of this study was to clarify the poten
tial role of IL-18 in the pathogenesis of the progressive inflammation and
fibrosis in biliary atresia (BA).
Methods: Six children with BA before hepatic portoenterostomy (HPE), 13 wit
h BA including 7 without jaundice and 6 with persistent jaundice after HPE,
and 16 healthy controls were examined. Blood samples were obtained preoper
atively from 6 patients, after HPE from 13, and after liver transplantation
from 4. The IL-18 level was determined by an enzyme-linked immunosorbent a
ssay (ELISA). Immunohistochemically, liver specimens from BA patients were
studied using a monoclonal antibody to macrophage-associated antigen (CD68)
.
Results: IL-18 levels were elevated in the patients before HPE compared wit
h those of the controls (349 +/- 54 pg/mL v 138 +/- 13 pg/mL, P < .0001). A
fter HPE, extremely high concentrations of IL-18 were observed in patients
with persistent jaundice (532 +/- 95 pg/mL, P < .0001), and the IL-18 level
s were significantly high even in the patients without jaundice (249 +/- 29
pg/mL, P < 0.005). The high IL-18 level lasted for a long time even in the
patients without jaundice after HPE. In contrast, the IL-18 levels immedia
tely decreased after liver transplantation. Immunohistochemically, the numb
er of CD68-positive Kupffer cells was significantly higher, and the size wa
s larger in the livers of the patients than in the controls. The proliferat
ion of CD68-positive cells was much more conspicuous in the liver specimens
obtained during liver transplantation than in those at the time of HPE.
Conclusions: Our findings showed elevation of serum IL-18 levels and activa
tion of Kupffer cells in BA. IL-18 released from activated Kupffer cells mi
ght play an important role in the pathophysiology of the progressive inflam
mation and fibrosis in BA. Furthermore, IL-18 level may be related to the p
rognosis in patients with BA. Copyright (C) 2000 by W.B. Saunders Company.