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本文引用的文献

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Organizing pneumonia and lymphoplasmacytic inflammation predict treatment response in idiopathic pulmonary fibrosis.机化性肺炎和淋巴细胞浆细胞性炎症可预测特发性肺纤维化的治疗反应。
Histopathology. 2007 Jan;50(2):258-65. doi: 10.1111/j.1365-2559.2006.02554.x.
2
Prognosis of fibrotic interstitial pneumonia: idiopathic versus collagen vascular disease-related subtypes.纤维化间质性肺炎的预后:特发性与胶原血管病相关亚型
Am J Respir Crit Care Med. 2007 Apr 1;175(7):705-11. doi: 10.1164/rccm.200607-912OC. Epub 2007 Jan 11.
3
Serious infections with antirheumatic therapy: are biologicals worse?抗风湿治疗引发的严重感染:生物制剂的情况更糟吗?
Ann Rheum Dis. 2006 Nov;65 Suppl 3(Suppl 3):iii54-7. doi: 10.1136/ard.2006.058503.
4
Fibroblast foci are not discrete sites of lung injury or repair: the fibroblast reticulum.成纤维细胞灶并非肺损伤或修复的离散部位:成纤维细胞网状结构。
Am J Respir Crit Care Med. 2006 Sep 15;174(6):654-8. doi: 10.1164/rccm.200602-205OC. Epub 2006 Jun 23.
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Circulating levels of B lymphocyte stimulator in patients with rheumatoid arthritis following rituximab treatment: relationships with B cell depletion, circulating antibodies, and clinical relapse.类风湿关节炎患者接受利妥昔单抗治疗后循环中B淋巴细胞刺激因子水平:与B细胞耗竭、循环抗体及临床复发的关系
Arthritis Rheum. 2006 Mar;54(3):723-32. doi: 10.1002/art.21650.
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Treatment for rheumatoid arthritis and the risk of hospitalization for pneumonia: associations with prednisone, disease-modifying antirheumatic drugs, and anti-tumor necrosis factor therapy.类风湿关节炎的治疗与肺炎住院风险:与泼尼松、改善病情抗风湿药及抗肿瘤坏死因子治疗的关联
Arthritis Rheum. 2006 Feb;54(2):628-34. doi: 10.1002/art.21568.
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The effects of tobacco smoking and rheumatoid factor seropositivity on disease activity and joint damage in early rheumatoid arthritis.吸烟和类风湿因子血清阳性对早期类风湿关节炎疾病活动度和关节损伤的影响。
Rheumatology (Oxford). 2006 Jun;45(6):734-40. doi: 10.1093/rheumatology/kei240. Epub 2006 Jan 10.
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A new model for an etiology of rheumatoid arthritis: smoking may trigger HLA-DR (shared epitope)-restricted immune reactions to autoantigens modified by citrullination.类风湿性关节炎病因的一种新模型:吸烟可能引发对经瓜氨酸化修饰的自身抗原的HLA - DR(共享表位)限制的免疫反应。
Arthritis Rheum. 2006 Jan;54(1):38-46. doi: 10.1002/art.21575.
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Safety and efficacy of rituximab in patients with rheumatoid arthritis refractory to disease modifying antirheumatic drugs and anti-tumor necrosis factor-alpha treatment.利妥昔单抗在对改善病情抗风湿药和抗肿瘤坏死因子-α治疗无效的类风湿关节炎患者中的安全性和有效性。
J Rheumatol. 2005 Nov;32(11):2109-15.
10
Gene expression profiles distinguish idiopathic pulmonary fibrosis from hypersensitivity pneumonitis.基因表达谱可区分特发性肺纤维化与过敏性肺炎。
Am J Respir Crit Care Med. 2006 Jan 15;173(2):188-98. doi: 10.1164/rccm.200504-644OC. Epub 2005 Sep 15.

类风湿性肺病

Rheumatoid lung disease.

作者信息

Brown Kevin K

机构信息

Department of Medicine, National Jewish Medical and Research Center, University of Colorado Health Sciences Center, Denver, Colorado, USA.

出版信息

Proc Am Thorac Soc. 2007 Aug 15;4(5):443-8. doi: 10.1513/pats.200703-045MS.

DOI:10.1513/pats.200703-045MS
PMID:17684286
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2647595/
Abstract

Rheumatoid arthritis (RA) is a common, functionally disabling disease with genetic and environmental contributors. It occurs in approximately 1% of the population and adversely affects quality of life, functional status, and survival. Beyond its impact on the joints, pulmonary involvement occurs regularly and is responsible for a significant portion of the morbidity and mortality. Although pulmonary infection and/or drug toxicity are frequent complications, lung disease directly associated with the underlying RA is more common. The airways, vasculature, parenchyma, and pleura can all be involved, with variable amounts of pathologic inflammation and fibrosis. The true adverse clinical impact of the most important of these directly associated disorders, RA-associated interstitial lung disease (RA-ILD), has only recently begun to reveal itself. Our knowledge of the underlying pathobiology and the impact of our current immunomodulatory and biologic therapies on the lung disease are less than incomplete. However, what is clear is the importance of progressive lung fibrosis in shortening survival and impairing quality of life in RA as well as in other connective tissue diseases. The impact of historically available and newer biologic therapies in altering the outcome of RA-ILD is unknown; translational studies focused on the pathobiology and clinical studies focused on the treatment of RA-ILD are needed.

摘要

类风湿关节炎(RA)是一种常见的、导致功能障碍的疾病,受遗传和环境因素影响。其发病率约为1%,对生活质量、功能状态和生存率产生不利影响。除了对关节的影响外,肺部受累也很常见,并且是发病和死亡的重要原因。虽然肺部感染和/或药物毒性是常见并发症,但与潜在RA直接相关的肺部疾病更为常见。气道、血管、实质和胸膜均可受累,病理炎症和纤维化程度各不相同。这些直接相关疾病中最重要的类风湿关节炎相关间质性肺病(RA-ILD)的真正不良临床影响直到最近才开始显现。我们对其潜在病理生物学以及当前免疫调节和生物疗法对肺部疾病影响的了解尚不完善。然而,清楚的是,进行性肺纤维化在缩短RA以及其他结缔组织疾病的生存期和损害生活质量方面的重要性。历史上可用的和更新的生物疗法对改变RA-ILD结局的影响尚不清楚;需要开展针对病理生物学的转化研究和针对RA-ILD治疗的临床研究。