增殖性狼疮肾炎的免疫介导和免疫抑制药物疗法。

IF 2.5 3区 医学 Q3 PHARMACOLOGY & PHARMACY
Expert Opinion on Pharmacotherapy Pub Date : 2024-10-01 Epub Date: 2024-10-14 DOI:10.1080/14656566.2024.2416038
Gabriella Moroni, Francesco Reggiani, Claudio Ponticelli
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引用次数: 0

摘要

导言增生性狼疮肾炎是系统性红斑狼疮常见的严重并发症。患者罹患慢性肾病、终末期肾病和肾外合并症的风险增加。近年来,由于治疗方案的进步,增殖性狼疮肾炎患者的预后有所改善。尽管取得了这些进展,狼疮性肾炎的治疗仍然十分复杂,而且仍有许多需求尚未得到满足:我们在主要数据库中进行了研究,以确定与狼疮性肾炎的免疫介导和免疫抑制疗法有关的最相关文章:专家观点:增殖性狼疮肾炎患者的预后仍然很严重。专家观点:增殖性狼疮肾炎患者的预后仍然十分严峻。用于该病的一些药物可能无法控制病情活动,而且大多数药物的治疗指数较低,可能会产生严重的副作用,危及生命。尽管如此,对传统药物更好的管理和新型疗法的引入改善了增殖性狼疮肾炎患者的肾脏预后,并减少了局部和全身不良反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immune-mediating and immunosuppressive pharmacotherapies for proliferative lupus nephritis.

Introduction: Proliferative lupus nephritis is a common and severe complication of systemic lupus erythematosus. Affected patients are at an increased risk of developing chronic kidney disease, end-stage kidney disease, and extra-renal comorbidities. In recent years, the prognosis for patients with proliferative lupus nephritis has improved thanks to advancements in management regimens. Despite these advances, lupus nephritis continues to present therapeutic complexities and unmet needs.

Areas covered: Research was conducted across major databases to identify the most relevant articles pertaining to immune-mediating and immunosuppressive therapies in lupus nephritis.

Expert opinion: The prognosis for patients with proliferative lupus nephritis remains severe. Some drugs used in this disease may be unable to control activity, and most of them have a low therapeutic index and may cause severe and life-threatening side effects. Nonetheless, better management of traditional drugs and the introduction of novel therapies have improved renal prognosis and reduced local and systemic adverse events in patients with proliferative lupus nephritis.

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来源期刊
CiteScore
5.60
自引率
3.10%
发文量
163
审稿时长
4-8 weeks
期刊介绍: Expert Opinion on Pharmacotherapy is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on newly approved/near to launch compounds mainly of chemical/synthetic origin, providing expert opinion on the likely impact of these new agents on existing pharmacotherapy of specific diseases.
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