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Treatment with nintedanib is as effective and safe in patients with other connective tissue diseases (CTDs)-interstitial lung disease (ILD) as in patients with systemic sclerosis-ILD: A multicenter retrospective study.与系统性硬化症相关间质性肺病(ILD)患者相比,尼达尼布治疗其他结缔组织病(CTD)相关ILD患者同样有效且安全:一项多中心回顾性研究。
Clin Rheumatol. 2025 Mar;44(3):1187-1195. doi: 10.1007/s10067-025-07323-0. Epub 2025 Feb 7.
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EULAR recommendations for the treatment of systemic sclerosis: 2023 update.欧洲抗风湿病联盟系统性硬化症治疗推荐:2023年更新版
Ann Rheum Dis. 2025 Jan;84(1):29-40. doi: 10.1136/ard-2024-226430. Epub 2025 Jan 2.
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Rheumatoid Arthritis-Associated Interstitial Lung Disease (RA-ILD): Update on Prevalence, Risk Factors, Pathogenesis, and Therapy.类风湿关节炎相关间质性肺疾病(RA-ILD):患病率、危险因素、发病机制和治疗的最新进展。
Curr Rheumatol Rep. 2024 Dec;26(12):431-449. doi: 10.1007/s11926-024-01155-8. Epub 2024 Sep 25.
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The 2024 British Society for Rheumatology guideline for management of systemic sclerosis.2024 年英国风湿病学会系统性硬化症管理指南。
Rheumatology (Oxford). 2024 Nov 1;63(11):2956-2975. doi: 10.1093/rheumatology/keae394.
5
2023 American College of Rheumatology (ACR)/American College of Chest Physicians (CHEST) Guideline for the Treatment of Interstitial Lung Disease in People with Systemic Autoimmune Rheumatic Diseases.2023 年美国风湿病学会(ACR)/美国胸科学会(CHEST)系统性自身免疫性风湿病患者间质性肺病治疗指南。
Arthritis Rheumatol. 2024 Aug;76(8):1182-1200. doi: 10.1002/art.42861. Epub 2024 Jul 8.
6
2023 American College of Rheumatology (ACR)/American College of Chest Physicians (CHEST) Guideline for the Screening and Monitoring of Interstitial Lung Disease in People with Systemic Autoimmune Rheumatic Diseases.2023 年美国风湿病学会(ACR)/美国胸科学会(CHEST)系统性自身免疫性风湿病患者间质性肺病筛查和监测指南。
Arthritis Care Res (Hoboken). 2024 Aug;76(8):1070-1082. doi: 10.1002/acr.25347. Epub 2024 Jul 8.
7
Nintedanib combined with immunosuppressive agents improves forced vital capacity in connective tissue disease-associated PF-ILD: a single-center study.尼达尼布联合免疫抑制剂可改善结缔组织病相关PF-ILD患者的用力肺活量:一项单中心研究。
BMC Rheumatol. 2024 Jun 18;8(1):27. doi: 10.1186/s41927-024-00400-y.
8
Clinical Characteristics and Outcomes of Interstitial Lung Disease in Primary Sjögren's Syndrome: A Retrospective Cohort Study.原发性干燥综合征间质性肺疾病的临床特征与结局:一项回顾性队列研究
Mediterr J Rheumatol. 2024 Jan 16;35(1):108-114. doi: 10.31138/mjr.230323.cca. eCollection 2024 Mar.
9
Safety and efficacy of rituximab in systemic sclerosis (DESIRES): open-label extension of a double-blind, investigators-initiated, randomised, placebo-controlled trial.利妥昔单抗治疗系统性硬化症的安全性和有效性(DESIRES):一项双盲、研究者发起、随机、安慰剂对照试验的开放性扩展。
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Anti-Ro52 positivity is associated with progressive interstitial lung disease in systemic sclerosis-an exploratory study.抗 Ro52 阳性与系统性硬化症的进行性间质性肺病相关:一项探索性研究。
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利妥昔单抗在结缔组织病相关间质性肺疾病中的应用:一项叙述性综述。

Use of rituximab in connective tissue disease-associated interstitial lung disease: a narrative review.

作者信息

Xu Chenhao, Xu Zewei, Ren Jin

机构信息

Department of Respiratory and Critical Care Medicine, The Second Hospital of Jilin University, Changchun, China.

Department of Cardiology, The Second Hospital of Jilin University, Changchun, China.

出版信息

Front Med (Lausanne). 2025 May 14;12:1555442. doi: 10.3389/fmed.2025.1555442. eCollection 2025.

DOI:10.3389/fmed.2025.1555442
PMID:40438359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12116372/
Abstract

This narrative review examines the therapeutic potential of rituximab, a monoclonal antibody targeting CD20 antigens, for treating connective tissue disease-associated interstitial lung disease. It outlines how rituximab offers a promising therapeutic option, particularly for patients who exhibit limited responses to standard therapies like glucocorticoids and immunosuppressive agents. Rituximab's mechanism of action, involving B lymphocyte depletion, contributes to attenuated inflammation and may slow pulmonary fibrosis progression. The article synthesizes findings from studies assessing rituximab's effects on lung function, clinical outcomes, and safety across distinct subtypes of connective tissue disease. It also discusses differential treatment responses based on disease characteristics and pathological subtypes, noting evidence that rituximab may be more effective as an initial treatment in some cases, though further investigation into long-term efficacy remains essential. Despite some associated risks, particularly infections, rituximab generally presents a favorable safety profile compared with conventional immunosuppressive therapies. Future research directions include optimizing dosing protocols, treatment intervals, and patient selection criteria, with emphasis on conducting rigorous, long-term randomized controlled trials to more definitively establish rituximab's role in managing interstitial lung disease in the context of connective tissue diseases.

摘要

本叙述性综述探讨了利妥昔单抗(一种靶向CD20抗原的单克隆抗体)治疗结缔组织病相关间质性肺病的治疗潜力。它概述了利妥昔单抗如何提供一种有前景的治疗选择,特别是对于那些对糖皮质激素和免疫抑制剂等标准疗法反应有限的患者。利妥昔单抗的作用机制包括B淋巴细胞耗竭,有助于减轻炎症,并可能减缓肺纤维化进展。本文综合了评估利妥昔单抗对不同结缔组织病亚型的肺功能、临床结局和安全性影响的研究结果。它还讨论了基于疾病特征和病理亚型的不同治疗反应,指出有证据表明利妥昔单抗在某些情况下作为初始治疗可能更有效,不过对其长期疗效的进一步研究仍然至关重要。尽管存在一些相关风险,特别是感染,但与传统免疫抑制疗法相比,利妥昔单抗总体上具有良好的安全性。未来的研究方向包括优化给药方案、治疗间隔和患者选择标准,重点是开展严格的长期随机对照试验,以更明确地确定利妥昔单抗在结缔组织病背景下管理间质性肺病中的作用。