Reply to: Is classifying SSc-ILD drugs as either immunosuppressive or anti-fibrotic misleading?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Rheumatology
Link
https://www.nature.com/articles/s41584-023-01014-3.pdf
Reference9 articles.
1. Pope, J. E. et al. State-of-the-art evidence in the treatment of systemic sclerosis. Nat. Rev. Rheumatol. 19, 212–226 (2023).
2. Andréasson, K. et al. Is classifying SSc-ILD drugs as either immunosuppressive or anti-fibrotic misleading? Nat. Rev. Rheumatol. https://doi.org/10.1038/s41584-023-01013-4 (2023).
3. Nambiar, A. M., Anzueto, A. R. & Peters, J. I. Effectiveness and safety of mycophenolate mofetil in idiopathic pulmonary fibrosis. PLoS ONE 12, e0176312 (2017).
4. Wigén, J., Elowsson-Rendin, L., Karlsson, L., Tykesson, E. & Westergren-Thorsson, G. Glycosaminoglycans: a link between development and regeneration in the lung. Stem Cells Dev. 28, 823–832 (2019).
5. Lescoat, A. et al. Combined anti-fibrotic and anti-inflammatory properties of JAK-inhibitors on macrophages in vitro and in vivo: perspectives for scleroderma-associated interstitial lung disease. Biochem. Pharmacol. 178, 114103 (2020).
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