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1型血小板反應蛋白7A域在膜性腎病中的研究進展

發(fā)布時間:2018-05-27 00:11

  本文選題:膜性腎病 + 特發(fā)性膜性腎病 ; 參考:《醫(yī)學研究生學報》2017年07期


【摘要】:在PLA2R1及其抗體研究的基礎上,1型血小板7A域及其抗體的發(fā)現(xiàn)使人們對膜性腎病又有了新的認識。THSD7A是在PLA2R1陰性的膜性腎病患者中發(fā)現(xiàn)的,故有部分研究報道提出PLA2R1與THSD7A的自身抗體在膜性腎病中相互排斥,但最新研究表明,THSD7A可與PLA2R1在膜性腎病患者中共存,呈現(xiàn)雙陽性。與PLA2R1類似,THSD7A對膜性腎病具有指導診斷、治療、監(jiān)測等意義。與PLA2R1不同的是,THSD7A在人類和嚙齒類動物的腎小球中均高度表達,故未來可利用小鼠模型研究THSD7A相關性膜性腎病的發(fā)病機制。文章就THSD7A及其抗體的結構、作用、與膜性腎病之間的關系及應用前景的研究進展進行綜述。
[Abstract]:Based on the study of PLA2R1 and its antibody, the discovery of type 1 platelet 7A domain and its antibody makes people have a new understanding of membranous nephropathy. THSD7A is found in patients with PLA2R1 negative membranous nephropathy. Therefore, some studies have reported that autoantibodies of PLA2R1 and THSD7A repel each other in membranous nephropathy, but the latest studies show that THSD7A and PLA2R1 co-exist in patients with membranous nephropathy and present double positive. Similar to PLA2R1, THSD 7 A has guiding significance in the diagnosis, treatment and monitoring of membranous nephropathy. Different from PLA2R1, THSD7A is highly expressed in human and rodent glomeruli, so we can use mouse model to study the pathogenesis of THSD7A associated membranous nephropathy in the future. In this paper, the structure, function, relationship between THSD7A and its antibodies to membranous nephropathy and their application prospect are reviewed.
【作者單位】: 南京醫(yī)科大學附屬無錫人民醫(yī)院檢驗科;江蘇省原子醫(yī)學研究所;
【基金】:江蘇省科技廳項目(BL2014022)
【分類號】:R692

【參考文獻】

相關期刊論文 前3條

1 錢玉s,

本文編號:1939539


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