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分子标志物还是临床终点?在资源有限的环境中,膜性肾病患者使用低剂量利妥昔单抗时,最佳监测工具是什么?

Molecular markers or clinical end points? What is the optimal monitoring tool for low-dose rituximab in membranous nephropathy in resource-limited settings?

作者信息

Mathew Gerry George

机构信息

Department of Nephrology, SRM Medical College Hospital and Research Centre, SRM Institute of Science and Technology, Kattankulathur, Chengalpattu, Tamil Nadu, 603203, India.

出版信息

J Nephrol. 2025 Jul;38(6):1717-1719. doi: 10.1007/s40620-025-02273-x. Epub 2025 Apr 7.

Abstract

Rituximab has been advocated for as the first treatment choice for idiopathic membranous nephropathy. Currently, low-dose rituximab protocols are being implemented for the treatment of primary membranous nephropathy with CD19 B-cell monitoring in resource-limited settings. CD19 monitoring is a recently established monitoring tool for determining the optimal response to rituximab treatment, especially when using low-dose rituximab. This manuscript identifies the problems encountered with rituximab treatment, pitfalls in CD19 monitoring and its performance in relation to conventional monitoring tools like anti-PLA2R levels, level of proteinuria, and estimated glomerular filtration rate (eGFR). This article highlights the utility of low-dose, tailor-made regimens of rituximab in the Indian subcontinent with CD19 B cell monitoring to verify appropriate clinical response, along with the economic benefits of such modified regimens in resource-limited settings, based on current scientific evidence.

摘要

利妥昔单抗已被提倡作为特发性膜性肾病的首选治疗药物。目前,在资源有限的环境中,正在实施低剂量利妥昔单抗方案,并通过监测CD19 B细胞来治疗原发性膜性肾病。CD19监测是一种最近建立的监测工具,用于确定对利妥昔单抗治疗的最佳反应,特别是在使用低剂量利妥昔单抗时。本手稿确定了利妥昔单抗治疗中遇到的问题、CD19监测中的陷阱及其与传统监测工具(如抗PLA2R水平、蛋白尿水平和估计肾小球滤过率(eGFR))相关的表现。本文基于当前科学证据,强调了在印度次大陆采用低剂量、量身定制的利妥昔单抗方案并结合CD19 B细胞监测以验证适当临床反应的实用性,以及这种改良方案在资源有限环境中的经济效益。

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