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利妥昔单抗治疗抗中性粒细胞胞浆抗体相关性血管炎二十年

Two Decades Rituximab Therapy in Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis.

作者信息

Habibi Mohammad Amin, Ahmadpour Sajjad, Tafaroji Javad, Eazi Seyed Mohammad, Minaee Poriya, Mohammadpour Yousef, Tavakolpour Soheil

机构信息

Department of Neurosurgery, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.

Patient Safety Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran.

出版信息

Curr Drug Targets. 2025;26(2):73-87. doi: 10.2174/0113894501323529240910015912.

Abstract

Remission failure and relapse numerate as one of the main problems in patients with antineutrophil cytoplasmic antibody-associated vasculitis (AAVs). The need for new agents that provide effective and safe induction accompanied by sustained remission seems to be urgent in clinical care. The efficacy and safety of rituximab (RTX) for AAVs therapy has been reported in various studies. RTX therapy offers several advantages to treating AAVs patients compared to other therapeutic approaches including reduction of Glucocorticoids (GCs) and conventional Immunosuppressive therapy (IST) usage during both the induction of remission and maintenance phases. This reduction can lead to a lower rate of serious complications making RTX therapy a safer option. It seems that RTX may provide improved clinical outcomes in these patients mediated via B-lymphocyte depletion, Proteinase 3-antineutrophilic cytoplasmic antibody (PR3-ANCA), and myeloperoxidase-antineutrophilic cytoplasmic antibody (MPO-ANCA) titers reduction. In this regard, some uncertainties have been reported to validate the association between such depletion and clinical improvement, as suggested by other sources of autoreactive B cells that did not target with RTX. Due to the prolonged B cell depletion, fixed intervals and adjusted dosage of RTX may be required in patients with AAVs. In this narrative review, we aimed to insight better understand regarding the efficacy of RTX for effective induction and sustained remission in patients with AAVs. It seems that discovering new biomarkers predicting relapse in AAVs patients can lead to future targeted therapy.

摘要

缓解失败和复发是抗中性粒细胞胞浆抗体相关性血管炎(AAV)患者的主要问题之一。在临床治疗中,迫切需要能提供有效且安全的诱导治疗并实现持续缓解的新型药物。多项研究报道了利妥昔单抗(RTX)治疗AAV的疗效和安全性。与其他治疗方法相比,RTX治疗为AAV患者带来了诸多优势,包括在诱导缓解期和维持期减少糖皮质激素(GCs)和传统免疫抑制治疗(IST)的使用。这种减少可降低严重并发症的发生率,使RTX治疗成为更安全的选择。RTX似乎可通过B淋巴细胞耗竭、蛋白酶3-抗中性粒细胞胞浆抗体(PR3-ANCA)和髓过氧化物酶-抗中性粒细胞胞浆抗体(MPO-ANCA)滴度降低,改善这些患者的临床结局。在这方面,正如其他未被RTX靶向的自身反应性B细胞来源所表明的,已报道了一些不确定性来验证这种耗竭与临床改善之间的关联。由于B细胞耗竭时间延长,AAV患者可能需要固定的时间间隔和调整后的RTX剂量。在这篇叙述性综述中,我们旨在更深入地了解RTX在AAV患者中有效诱导和持续缓解的疗效。似乎发现预测AAV患者复发的新生物标志物可引领未来的靶向治疗。

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