TY - JOUR
T1 - Autoantibody against caspase-3, an executioner of apoptosis, in patients with systemic sclerosis
AU - Okazaki, Shihoko
AU - Ogawa, Fumihide
AU - Iwata, Yohei
AU - Hara, Toshihide
AU - Muroi, Eiji
AU - Komura, Kazuhiro
AU - Takenaka, Motoi
AU - Shimizu, Kazuhiro
AU - Hasegawa, Minoru
AU - Fujimoto, Manabu
AU - Sato, Shinichi
N1 - Funding Information:
Acknowledgments This work was supported by a grant of Research on Intractable Diseases from the Ministry of Health, Labour and Welfare of Japan.
PY - 2010/5
Y1 - 2010/5
N2 - The objective of the study was to determine the presence or levels of antibodies (Abs) against caspase-3 and their clinical relevance in systemic sclerosis (SSc). Anti-caspase-3 Ab was examined by enzyme-linked immunosorbent assay and immunoblotting. IgG anti-caspase-3 Ab levels in SSc patients were higher than in normal controls. SSc patients positive for IgG anti-caspase-3 Ab had significantly longer disease duration, more frequent presence of decreased %VC and %DLco, and elevated levels of serum immunoglobulin and erythrocyte sedimentation rates. IgG anti-caspase-3 Ab levels correlated positively with serum IgG levels, renal vascular resistance, and serum levels of 8-isoprostane. Immunoblotting analysis confirmed the presence of anti-caspase-3 Ab in sera from SSc patients. Caspase-3 enzymatic activity was inhibited by IgG isolated from SSc sera containing IgG anti-caspase-3 Ab. These results suggest that autoantibody against caspase-3 is generated in SSc and that this Ab is related to the severity of pulmonary fibrosis, vascular damage, and inflammation.
AB - The objective of the study was to determine the presence or levels of antibodies (Abs) against caspase-3 and their clinical relevance in systemic sclerosis (SSc). Anti-caspase-3 Ab was examined by enzyme-linked immunosorbent assay and immunoblotting. IgG anti-caspase-3 Ab levels in SSc patients were higher than in normal controls. SSc patients positive for IgG anti-caspase-3 Ab had significantly longer disease duration, more frequent presence of decreased %VC and %DLco, and elevated levels of serum immunoglobulin and erythrocyte sedimentation rates. IgG anti-caspase-3 Ab levels correlated positively with serum IgG levels, renal vascular resistance, and serum levels of 8-isoprostane. Immunoblotting analysis confirmed the presence of anti-caspase-3 Ab in sera from SSc patients. Caspase-3 enzymatic activity was inhibited by IgG isolated from SSc sera containing IgG anti-caspase-3 Ab. These results suggest that autoantibody against caspase-3 is generated in SSc and that this Ab is related to the severity of pulmonary fibrosis, vascular damage, and inflammation.
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U2 - 10.1007/s00296-009-1068-3
DO - 10.1007/s00296-009-1068-3
M3 - Article
C2 - 19639321
AN - SCOPUS:77955094748
SN - 0172-8172
VL - 30
SP - 871
EP - 878
JO - Rheumatology International
JF - Rheumatology International
IS - 7
ER -