TY - JOUR
T1 - Serum levels of interleukin-18-binding protein isoform a
T2 - Clinical association with inflammation and pulmonary hypertension in systemic sclerosis
AU - Nakamura, Kouki
AU - Asano, Yoshihide
AU - Taniguchi, Takashi
AU - Minatsuki, Shun
AU - Inaba, Toshiro
AU - Maki, Hisataka
AU - Hatano, Masaru
AU - Yamashita, Takashi
AU - Saigusa, Ryosuke
AU - Ichimura, Yohei
AU - Takahashi, Takehiro
AU - Toyama, Tetsuo
AU - Yoshizaki, Ayumi
AU - Miyagaki, Tomomitsu
AU - Sugaya, Makoto
AU - Sato, Shinichi
N1 - Funding Information:
This work was supported by a grant for Research on Intractable Diseases from the Ministry of Health, Labor, and Welfare of Japan.
Publisher Copyright:
© 2016 Japanese Dermatological Association
PY - 2016/8/1
Y1 - 2016/8/1
N2 - Systemic sclerosis (SSc) is a chronic autoimmune inflammatory disease characterized by extensive tissue fibrosis and various vascular complications. A wealth of evidence suggests the substantial contribution of pro-inflammatory cytokines to the development of SSc, but the role of interleukin (IL)-18 signaling in this disease still remains elusive. To address this issue, we herein determined serum levels of IL-18-binding protein isoform a (IL-18BPa), a soluble decoy receptor for IL-18, by enzyme-linked immunosorbent assay in 57 SSc patients and 20 healthy controls and evaluated their clinical correlation. Serum IL-18BPa levels were higher in SSc patients than in healthy controls, while comparable between diffuse cutaneous SSc and limited cutaneous SSc patients. Although serum IL-18BPa levels were not associated with dermal and pulmonary fibrotic parameters in SSc patients, there was a significant positive correlation between serum IL-18BPa levels and right ventricular systolic pressure estimated by echocardiography. Furthermore, in 24 SSc patients who underwent right heart catheterization, serum IL-18BPa levels positively correlated with mean pulmonary arterial pressure. As for systemic inflammatory markers, significant positive correlations of circulating IL-18BPa levels with erythrocyte sedimentation rate and C-reactive protein were noted. These results suggest that the inhibition of IL-18 signaling by IL-18BPa may be involved in the development of pulmonary vascular involvement leading to pulmonary hypertension and modulate the systemic inflammation in SSc.
AB - Systemic sclerosis (SSc) is a chronic autoimmune inflammatory disease characterized by extensive tissue fibrosis and various vascular complications. A wealth of evidence suggests the substantial contribution of pro-inflammatory cytokines to the development of SSc, but the role of interleukin (IL)-18 signaling in this disease still remains elusive. To address this issue, we herein determined serum levels of IL-18-binding protein isoform a (IL-18BPa), a soluble decoy receptor for IL-18, by enzyme-linked immunosorbent assay in 57 SSc patients and 20 healthy controls and evaluated their clinical correlation. Serum IL-18BPa levels were higher in SSc patients than in healthy controls, while comparable between diffuse cutaneous SSc and limited cutaneous SSc patients. Although serum IL-18BPa levels were not associated with dermal and pulmonary fibrotic parameters in SSc patients, there was a significant positive correlation between serum IL-18BPa levels and right ventricular systolic pressure estimated by echocardiography. Furthermore, in 24 SSc patients who underwent right heart catheterization, serum IL-18BPa levels positively correlated with mean pulmonary arterial pressure. As for systemic inflammatory markers, significant positive correlations of circulating IL-18BPa levels with erythrocyte sedimentation rate and C-reactive protein were noted. These results suggest that the inhibition of IL-18 signaling by IL-18BPa may be involved in the development of pulmonary vascular involvement leading to pulmonary hypertension and modulate the systemic inflammation in SSc.
KW - inflammation
KW - interleukin-18
KW - interleukin-18-binding protein
KW - pulmonary hypertension
KW - systemic sclerosis
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U2 - 10.1111/1346-8138.13252
DO - 10.1111/1346-8138.13252
M3 - Article
C2 - 26777734
AN - SCOPUS:84980368712
SN - 0385-2407
VL - 43
SP - 912
EP - 918
JO - Journal of Dermatology
JF - Journal of Dermatology
IS - 8
ER -