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狼疮性肾炎的危险因素和生物标志物:研究进展。

Lupus Nephritis Risk Factors and Biomarkers: An Update.

机构信息

Department of Immunology, Referral Medical Biology Laboratory, University Hospital of Toulouse, Institut National de la Santé Et de la Recherche Médicale (INSERM) U1291, Centre National de la Recherche Scientifique (CNRS) U5051, 31400 Toulouse, France.

Department of Chemistry, University of South Florida, Tampa, FL 33620, USA.

出版信息

Int J Mol Sci. 2023 Sep 25;24(19):14526. doi: 10.3390/ijms241914526.

DOI:10.3390/ijms241914526
PMID:37833974
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10572905/
Abstract

Lupus nephritis (LN) represents the most severe organ manifestation of systemic lupus erythematosus (SLE) in terms of morbidity and mortality. To reduce these risks, tremendous efforts have been made in the last decade to characterize the different steps of the disease and to develop biomarkers in order to better (i) unravel the pre-SLE stage (e.g., anti-nuclear antibodies and interferon signature); (ii) more timely initiation of therapy by improving early and accurate LN diagnosis (e.g., pathologic classification was revised); (iii) monitor disease activity and therapeutic response (e.g., recommendation to re-biopsy, new urinary biomarkers); (iv) prevent disease flares (e.g., serologic and urinary biomarkers); (v) mitigate the deterioration in the renal function; and (vi) reduce side effects with new therapeutic guidelines and novel therapies. However, progress is poor in terms of improvement with early death attributed to active SLE or infections, while later deaths are related to the chronicity of the disease and the use of toxic therapies. Consequently, an individualized treat-to-target strategy is mandatory, and for that, there is an unmet need to develop a set of accurate biomarkers to be used as the standard of care and adapted to each stage of the disease.

摘要

狼疮肾炎 (LN) 是系统性红斑狼疮 (SLE) 最严重的器官表现,在发病率和死亡率方面都是如此。为了降低这些风险,在过去十年中,人们做出了巨大努力来描述疾病的不同阶段,并开发生物标志物,以便更好地:(i) 揭示狼疮前阶段(例如,抗核抗体和干扰素特征);(ii) 通过改善早期和准确的 LN 诊断来更及时地开始治疗(例如,病理分类进行了修订);(iii) 监测疾病活动和治疗反应(例如,建议重新进行活检,新的尿液生物标志物);(iv) 预防疾病发作(例如,血清学和尿液生物标志物);(v) 减轻肾功能恶化;以及 (vi) 用新的治疗指南和新的治疗方法减少副作用。然而,在改善方面进展甚微,早期死亡归因于活跃的 SLE 或感染,而晚期死亡与疾病的慢性化和有毒治疗有关。因此,必须采取个体化的治疗目标策略,为此,需要开发一组准确的生物标志物作为标准护理,并适应疾病的每个阶段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c92/10572905/de32616b2f33/ijms-24-14526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c92/10572905/72304570ce9c/ijms-24-14526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c92/10572905/de32616b2f33/ijms-24-14526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c92/10572905/72304570ce9c/ijms-24-14526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3c92/10572905/de32616b2f33/ijms-24-14526-g002.jpg

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