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Autoantibody against activating transcription factor-2 in patients with systemic sclerosis


Y. Akiyama, F. Ogawa, Y. Iwata, K. Komura, T. Hara, E. Muroi, S.-J. Bae, M. Takenaka, K. Shimizu, M. Hasegawa, M. Fujimoto, S. Sato

 

CER3667
2009 Vol.27, N°5
PI 0751, PF 0757
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PMID: 19917156 [PubMed]

Abstract

OBJECTIVES:
To determine the prevalence and clinical correlation of autoantibody to activating transcription factor (ATF)-2, a transcription factor of ATF/CREB family, in patients with systemic sclerosis (SSc).
METHODS:
Anti-ATF-2 Ab was examined by ELISA and immunoblotting using human recombinant ATF-2. ATF-2 activity to bind target DNA was evaluated by ELISA using a plate coated with oligonucleotide containing the consensus binding site for ATF-2.
RESULTS:
IgG anti-ATF-2 Ab levels in SSc patients (n=69) were significantly higher than those in normal controls (n=26). SSc patients positive for IgG anti-ATF-2 Ab had significantly longer disease duration, more frequent presence of decreased %VC and %DLco, and elevated levels of serum IgG, serum IgA, and erythrocyte sedimentation rates than those negative. More-over, IgG anti-ATF-2 Ab levels correlated inversely with %VC or %DLco. The presence of anti-ATF-2 Ab in SSc patients was confirmed by immunoblotting analysis. IgG isolated from serum samples of SSc patients positive for IgG anti-ATF-2 Ab by ELISA slightly but significantly inhibited ATF-2 activity compared with normal controls.
CONCLUSIONS:
These results suggest that anti-ATF-2 Ab is a new autoantibody in SSc and that it serves as a novel serological marker for inflammation and lung involvement in SSc.

Rheumatology Article