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自身免疫性肾小球肾炎及抗体介导的移植排斥反应中针对抗氧化酶的抗体

Antibodies Against Anti-Oxidant Enzymes in Autoimmune Glomerulonephritis and in Antibody-Mediated Graft Rejection.

作者信息

Bruschi Maurizio, Candiano Giovanni, Petretto Andrea, Angeletti Andrea, Meroni Pier Luigi, Prunotto Marco, Ghiggeri Gian Marco

机构信息

Unit of Nephrology, Dialysis and Transplantation and Laboratory of Molecular Nephrology, Core Facilities-Proteomics Laboratory, 16147 Genoa, Italy.

Department of Experimental Medicine (DIMES), University of Genoa, 16132 Genoa, Italy.

出版信息

Antioxidants (Basel). 2024 Dec 12;13(12):1519. doi: 10.3390/antiox13121519.

Abstract

Historically, oxidants have been considered mechanisms of glomerulonephritis, but a direct cause-effect correlation has never been demonstrated. Several findings in the experimental model of autoimmune conditions with renal manifestations point to the up-regulation of an oxidant/anti-oxidant system after the initial deposition of autoantibodies in glomeruli. Traces of oxidants in glomeruli cannot be directly measured for their rapid metabolism, while indirect proof of their implications is derived from the observation that Superoxide Oxidase 2 (SOD2) is generated by podocytes after autoimmune stress. The up-regulation of other anti-oxidant systems takes place as well. Here, we discuss the concept that a second wave of antibodies targeting SOD2 is generated in autoimmune glomerulonephritis and may negatively influence the clinical outcome. Circulating and renal deposits of anti-SOD2 antibodies have been detected in patients with membranous nephropathy and lupus nephritis, two main examples of autoimmune disease of the kidney, which correlate with the clinical outcome. The presence of anti-SOD2 antibodies in circulation and in the kidney has been interpreted as a mechanism which modifies the normal tissue response to oxidative stress. Overall, these findings repropose the role of the oxidant/anti-oxidant balance in autoimmune glomerulonephritis. The same conclusion on the oxidant/anti-oxidant balance may be proposed in renal transplant. Patients receiving a renal graft may develop antibodies specific for Glutathione Synthetase (GST), which modulates the amount of GST disposable for rapid scavenging of reactive oxygen species (ROS). The presence of anti-GST antibodies in serum is a major cause of rejection. The perspective is to utilize molecules with known anti-oxidant effects to modulate the anti-oxidative response in autoimmune pathology of the kidney. A lot of molecules with known anti-oxidant effects can be utilized, many of which have already been proven effective in animal models of autoimmune glomerulonephritis. Many molecules with anti-oxidant activity are natural products; in some cases, they are constituents of diets. Owing to the simplicity of these drugs and the absence of important adverse effects, many anti-oxidants could be directly utilized in human beings.

摘要

从历史上看,氧化剂一直被认为是肾小球肾炎的发病机制,但从未证实过直接的因果关系。在具有肾脏表现的自身免疫性疾病实验模型中的一些发现表明,自身抗体最初在肾小球中沉积后,氧化/抗氧化系统会上调。由于氧化剂代谢迅速,无法直接测量肾小球中的氧化剂痕迹,而其作用的间接证据来自于观察到足细胞在自身免疫应激后会产生超氧化物歧化酶2(SOD2)。其他抗氧化系统也会上调。在此,我们讨论了自身免疫性肾小球肾炎中会产生靶向SOD2的第二波抗体这一概念,且这可能会对临床结果产生负面影响。在膜性肾病和狼疮性肾炎患者中检测到了抗SOD2抗体的循环和肾脏沉积,这两种疾病是肾脏自身免疫性疾病的主要例子,且与临床结果相关。循环中和肾脏中抗SOD2抗体的存在被解释为一种改变正常组织对氧化应激反应的机制。总体而言,这些发现再次提出了氧化/抗氧化平衡在自身免疫性肾小球肾炎中的作用。在肾移植中也可能得出关于氧化/抗氧化平衡的相同结论。接受肾移植的患者可能会产生针对谷胱甘肽合成酶(GST)的特异性抗体,该酶可调节用于快速清除活性氧(ROS)的GST量。血清中抗GST抗体的存在是排斥反应的主要原因。前景是利用具有已知抗氧化作用的分子来调节肾脏自身免疫性病理中的抗氧化反应。可以利用许多具有已知抗氧化作用的分子,其中许多已在自身免疫性肾小球肾炎动物模型中被证明有效。许多具有抗氧化活性的分子是天然产物;在某些情况下,它们是饮食的组成成分。由于这些药物简单且无重要不良反应,许多抗氧化剂可直接用于人类。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/166d/11726969/4dca4894a3ae/antioxidants-13-01519-g001.jpg

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