Pathogenesis of the Novel Autoimmune-Associated Long-QT Syndrome | |
Article | |
关键词: CONGENITAL HEART-BLOCK; ANTI-RO/SSA; INTERVAL PROLONGATION; CELLULAR BASIS; CARDIAC-ARRHYTHMIAS; CALCIUM-CHANNELS; POSITIVE ADULTS; REPOLARIZATION; ANTIBODIES; CHILDREN; | |
DOI : 10.1161/CIRCULATIONAHA.115.009800 | |
来源: SCIE |
【 摘 要 】
Background-Emerging clinical evidence demonstrates high prevalence of QTc prolongation and complex ventricular arrhythmias in patients with anti-Ro antibody (anti-Ro Ab)-positive autoimmune diseases. We tested the hypothesis that anti-Ro Abs target the HERG (human ether-a-go-go-related gene) K+ channel, which conducts the rapidly activating delayed K+ current, I-Kr, thereby causing delayed repolarization seen as QT interval prolongation on the ECG. Methods and Results-Anti-Ro Ab-positive sera, purified IgG, and affinity-purified anti-52kDa Ro Abs from patients with autoimmune diseases and QTc prolongation were tested on I-Kr using HEK293 cells expressing HERG channel and native cardiac myocytes. Electrophysiological and biochemical data demonstrate that anti-Ro Abs inhibit I-Kr to prolong action potential duration by directly binding to the HERG channel protein. The 52-kDa Ro antigen-immunized guinea pigs showed QTc prolongation on ECG after developing high titers of anti-Ro Abs, which inhibited native I-Kr and cross-reacted with guinea pig ERG channel. Conclusions-The data establish that anti-Ro Abs from patients with autoimmune diseases inhibit I-Kr by cross-reacting with the HERG channel likely at the pore region where homology between anti-52-kDa Ro antigen and HERG channel is present. The animal model of autoimmune-associated QTc prolongation is the first to provide strong evidence for a pathogenic role of anti-Ro Abs in the development of QTc prolongation. It is proposed that adult patients with anti-Ro Abs may benefit from routine ECG screening and that those with QTc prolongation should receive counseling about drugs that may increase the risk for life-threatening arrhythmias.
【 授权许可】
Free