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Induction of autoimmune response to the extracellular loop of the HERG channel pore induces QTc prolongation in guinea‐pigs

机译:对HERG通道孔的细胞外环的自身免疫反应的诱导导致豚鼠QTc延长

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摘要

Key points class="unordered" style="list-style-type:disc" id="tjp7380-list-0001">Channelopathies of autoimmune origin are novel and are associated with corrected QT (QTc) prolongation and complex ventricular arrhythmias.We have recently demonstrated that anti‐SSA/Ro antibodies from patients with autoimmune diseases and with QTc prolongation on the ECG target the human ether‐à‐go‐go‐related gene (HERG) K+ channel by inhibiting the corresponding current, I Kr, at the pore region.Immunization of guinea‐pigs with a peptide (E‐pore peptide) corresponding to the extracellular loop region connecting the S5 and S6 segments of the HERG channel induces high titres of antibodies that inhibit I Kr, lengthen the action potential and cause QTc prolongation on the surface ECG. In addition, anti‐SSA/Ro‐positive sera from patients with connective tissue diseases showed high reactivity to the E‐pore peptide.The translational impact is the development of a peptide‐based approach for the diagnosis and treatment of autoimmune‐associated long QT syndrome.
机译:关键点 class =“ unordered” style =“ list-style-type:disc” id =“ tjp7380-list-0001”> <!-list-behavior = unordered prefix-word = mark-type = disc max- label-size = 0-> 自身免疫性起源的通道病是新颖的,与纠正的QT(QTc)延长和复杂的室性心律失常有关。 我们最近证明了抗SSA / Ro抗体来自自身免疫性疾病且QTc在ECG上延长的患者通过抑制毛孔中相应的电流I Kr靶向人类以太相关基因(HERG)K + 通道 用对应于连接HERG通道S5和S6区段的细胞外环区的肽(E孔肽)免疫豚鼠,会诱导高滴度的抗体抑制I Kr,延长动作电位并导致表面ECG的QTc延长。此外,结缔组织病患者的抗SSA / Ro阳性血清对E-pore肽显示出高反应性。 翻译的影响是基于肽的诊断和诊断方法的发展。自身免疫相关的长QT综合征的治疗。

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