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Targeted therapies in interstitial lung disease secondary to systemic autoimmune rheumatic disease. Current status and future development

期刊

AUTOIMMUNITY REVIEWS
卷 20, 期 2, 页码 -

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ELSEVIER
DOI: 10.1016/j.autrev.2020.102742

关键词

Autoimmune rheumatic diseases; Interstitial lung disease; Rheumatoid arthritis; Sjogren's syndrome; Vasculitis; Myositis; Scleroderma immunosuppressive drugs; Targeted treatment; Anti-fibrotic treatment

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Autoimmune rheumatic diseases (ARD) involve multiple organ systems, including the lungs, where Interstitial Lung Disease (ILD) is a common manifestation. Current first-line treatments include corticosteroids and immunosuppressive drugs, while targeted therapies like biological DMARDS and anti-fibrotic agents are emerging as new options for treatment.
Autoimmune rheumatic diseases (ARD) are characterized by systemic manifestations and multiple organ involvement, including the lung. Interstitial Lung Disease (ILD) is a cardinal manifestation of lung involvement in patients with ARD and is associated with significant morbidity and mortality. Corticosteroids and immunosuppressive drugs are used as first -line treatment. Targeted therapies, such as biological disease modifying anti-rheumatic drugs (DMARDS) and anti- fibrotic agents are new treatment options. In this review we discuss the role of targeted therapies in patients with ILD secondary to ARD.

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