2024年肾脏病学的亮点

Camille Cohen
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摘要

2024年标志着肾脏病学的重大进展,特别是在免疫球蛋白A (IgA)肾病和肾保护方面。在IgA肾病中,针对BAFF和APRIL通路的sibeprelimab和atacicept等新分子显示出蛋白尿的减少和肾小球滤过率(GFR)的稳定,证实了这些通路在该疾病中的重要性。此外,微生物群在病理中的参与开辟了有希望的治疗前景。在肾保护方面,SGLT2抑制剂、内皮素受体和GLP1激动剂联合使用可增强慢性肾脏疾病(包括糖尿病肾病)的管理,对蛋白尿和肾脏生存有积极影响。在特发性肾病综合征(INS)中发现抗nephrin抗体标志着向前迈出了重要的一步,可以更好地预测对免疫抑制剂的反应,更精确地诊断自身免疫和遗传病理,并为该病理的更个性化管理开辟了未来的前景。来自血液学的抗cd38疗法在肾小球疾病中也显示出有希望的结果,而CAR-T细胞正在为难治性自身免疫性疾病(如狼疮)开辟新的治疗选择。这些进步证明了肾病学向精准医学的迈进,其中个性化治疗可以及时显著改善肾脏病变患者的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The highlights of nephrology in 2024

The year 2024 marks significant progress in nephrology, particularly in immunoglobulin A (IgA) nephropathy and nephroprotection. In IgA nephropathy, new molecules such as sibeprenlimab and atacicept, targeting the BAFF and APRIL pathways, have shown a reduction in proteinuria and stabilization of glomerular filtration rate (GFR), confirming the importance of these pathways in the disease. Furthermore, the involvement of the microbiota in the pathology opens up promising therapeutic prospects. In nephroprotection, the combination of SGLT2 inhibitors, endothelin receptors and GLP1 agonists enhances the management of chronic kidney disease, including diabetic nephropathy, with positive effects on proteinuria and renal survival. The discovery of anti-nephrin antibodies in idiopathic nephrotic syndrome (INS) marks a major step forward, enabling better prediction of the response to immunosuppressants and a more refined diagnosis between autoimmune and genetic pathologies, and opening up the future prospect of more personalized management of this pathology. Derived from hematology, anti-CD38 therapies are also showing promising results in glomerulopathies, while CAR-T cells are opening the way to new therapeutic options for refractory autoimmune diseases such as lupus. These advances testify to a move towards precision medicine in nephrology, where the personalization of treatments could, in time, significantly improve the management of patients with kidney pathologies.

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