利妥昔单抗治疗自身免疫性疾病患者的低丙种球蛋白血症和感染事件:10年实际生活经验。

IF 7.2 2区 医学 Q1 IMMUNOLOGY
Yuxue Nie, Nianyi Zhang, Jingna Li, Di Wu, Yunjiao Yang, Li Zhang, Wei Bai, Nan Jiang, Lin Qiao, Can Huang, Shuang Zhou, Xinping Tian, Mengtao Li, Xiaofeng Zeng, Linyi Peng, Wen Zhang
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引用次数: 0

摘要

目的研究接受利妥昔单抗(RTX)治疗的自身免疫性疾病(AID)患者低丙种球蛋白血症(HGG)和严重感染事件(SIE)的预测因素:这是一项在中国一家三级医疗中心进行的回顾性研究。采用Cox分析评估了HGG或SIE的预测因素。采用限制性立方样条曲线(RCS)分析法研究糖皮质激素(GC)维持剂量与SIE之间的相关性:本研究共纳入 219 例患者,累计随访时间为 698.28 人年。在研究人群中,117 名患者被诊断患有结缔组织病,75 名患者出现 ANCA 相关性血管炎,27 名患者表现出 IgG4 相关性疾病。63.3%的患者出现 HGG,RTX 开始三个月后,IgG 和 IgM 明显下降。SIE发生率为每100人年7.2例。GC 维持剂量的增加是低 IgG(HR 1.07,95% CI 1.02-1.12,p = 0.003)和 SIE(HR 1.06,95% CI 1.02-1.1,p = 0.004)的独立风险因素。进一步的RCS分析发现,7.48 mg/d泼尼松是接受RTX治疗的患者避免SIE风险显著增加的安全阈值剂量:结论:HGG在接受RTX治疗的AID患者中较为常见。结论:HGG在RTX治疗的AID患者中较为常见,患有慢性肺部疾病或在RTX治疗期间服用≥7.5 mg/d泼尼松的患者发生SIE的风险增加,需要引起医生的注意。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hypogammaglobulinemia and Infection Events in Patients with Autoimmune Diseases Treated with Rituximab: 10 Years Real-Life Experience.

Hypogammaglobulinemia and Infection Events in Patients with Autoimmune Diseases Treated with Rituximab: 10 Years Real-Life Experience.

Objectives: To investigate predictors of hypogammaglobulinemia (HGG) and severe infection event (SIE) in patients with autoimmune disease (AID) receiving rituximab (RTX) therapy.

Methods: This was a retrospective study conducted in a tertiary medical center in China. Predictors of HGG or SIE were assessed using Cox analysis. Restricted cubic spline (RCS) analysis was applied to examine the correlation between glucocorticoid (GC) maintenance dose and SIE.

Results: A total of 219 patients were included in this study, with a cumulative follow-up time of 698.28 person-years. Within the study population, 117 patients were diagnosed with connective tissue disease, 75 patients presented with ANCA-associated vasculitis, and 27 patients exhibited IgG4-related disease. HGG was reported in 63.3% of the patients, where an obvious decline in IgG and IgM was shown three months after RTX initiation. The rate of SIE was 7.2 per 100 person-years. An increase in the GC maintenance dose was an independent risk factor for both hypo-IgG (HR 1.07, 95% CI 1.02-1.12, p = 0.003) and SIE (HR 1.06, 95% CI 1.02-1.1, p = 0.004). Further RCS analysis identified 7.48 mg/d prednisone as a safe threshold dose for patients who underwent RTX treatment to avoid a significantly increased risk for SIE.

Conclusion: HGG was relatively common in RTX-treated AID patients. Patients with chronic lung disease or who were taking ≥ 7.5 mg/d prednisone during RTX treatment were at increased risk for SIE and warrant attention from physicians.

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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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