Interstitial lung disease in connective tissue diseases: evolving concepts of pathogenesis and management

被引:170
作者
Castelino, Flavia V. [1 ]
Varga, John [2 ]
机构
[1] Harvard Univ, Sch Med, Div Rheumatol, Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Northwestern Univ, Feinberg Sch Med, Div Rheumatol, Chicago, IL 60611 USA
关键词
GROWTH-FACTOR-BETA; PLACEBO-CONTROLLED TRIAL; CLINICALLY AMYOPATHIC DERMATOMYOSITIS; RESOLUTION COMPUTED-TOMOGRAPHY; INDUCED PULMONARY-FIBROSIS; SYSTEMIC-SCLEROSIS; RHEUMATOID-ARTHRITIS; MYCOPHENOLATE-MOFETIL; IMATINIB MESYLATE; FIBROBLAST ACTIVATION;
D O I
10.1186/ar3097
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Interstitial lung disease (ILD) is a challenging clinical entity associated with multiple connective tissue diseases, and is a significant cause of morbidity and mortality. Effective therapies for connective tissue disease-associated interstitial lung disease (CTD-ILD) are still lacking. Multidisciplinary clinics dedicated to the early diagnosis and improved management of patients with CTD-ILD are now being established. There is rapid progress in understanding and identifying the effector cells, the proinflammatory and profibrotic mediators, and the pathways involved in the pathogenesis of CTD-ILD. Serum biomarkers may provide new insights as risk factors for pulmonary fibrosis and as measures of disease progression. Despite these recent advances, the management of patients with CTD-ILD remains suboptimal. Further studies are therefore urgently needed to better understand these conditions, and to develop effective therapeutic interventions.
引用
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页数:11
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