G-protein coupled receptor auto-antibodies in thromboangiitis obliterans (Buergers disease) and their removal by immunoadsorption

免疫吸附 受体 自身抗体 内皮素受体 医学 G蛋白偶联受体 伯格氏病 抗体 免疫学 内科学 疾病
作者
Peter Klein‐Weigel,Marion Bimmler,Petra Hempel,Sebastian Schöpp,Siegrid Dreusicke,Jana Valerius,Anne Bohlen,Joana M. Boehnlein,Daniel Bestler,Stephanie Funk,Saban Elitok
出处
期刊:VASA [Hogrefe Publishing Group]
卷期号:43 (5): 347-352 被引量:31
标识
DOI:10.1024/0301-1526/a000372
摘要

Background: Immunhistopathological and serological data favors an immunopathogenesis of thromboangiitis onliterans(TAO, Buerger’s disease). Autoantbodies seem to play a major role. Immunoadsorption (IA) proved to be therapeutically effective. We focused on agonistic autoantibodies (agAAB) directed against G-protein coupled receptors (GPCR) and proved the hypothesis, that these agAAB might be present in TAO and that a five day course of IA might be able to eliminate these agAAB effectively. Patients and methods: Between December 2012 and May 2014 11 TAO-patients were treated by IA in a five day course. AgAAB-analysis was performed using specific ELISA techniques. Results: AgAAB were detected in 9 out of 11 patients (81.8 %).Multiple agAAB were present in 7 patients (63.6 %). A clustering of agAAB directed against loop1 of the adrenergic α1-receptor and the endothelin-A-(ETA)receptor was identified, representing 72.7 % resp. 54.5 % of the patients. AgAAB directed against the angiotensin-1 (AT-1) epitope 1 or 2 were detected in 3 patients and agAAB directed against protease-activated receptor (PAR) loop1/2 were seen in 2 patients. AgAAB directed against ETA-receptor loop1 never appeared without agAAB directed against α1-receptor loop1. Immediately after a five day-course of IA agAAB were absent in 81.8 % of the total study group and in 77.8 % of all cases tested positive for agAAB before IA. Conclusions: AgAAB directed against GPCR were identified in TAO patients with a clustering of agAAB directed against α-1-adrenergic receptor loop1 and ETA-receptor loop1. AgAA were eliminated by IA in the majority of cases. We suggest that these agAA play an important role in the pathogenesis of TAO and that their elimination might be responsible for the positive therapeutic effects reported in patients treated with IA.
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