In 2015, new tools were developed to modulate fibroblast and macrophage activity to halt liver fibrogenesis and stimulate resolution. Essential factors for resolution were identified and clinical trials yielded potential new antifibrotic drugs. Although innovations were made this year, clinical trials are still hampered by the lack of methods to monitor disease progression.
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References
Palumbo-Zerr, K. et al. Orphan nuclear receptor NR4A1 regulates transforming growth factor-β signaling and fibrosis. Nat. Med. 21, 150–158 (2015).
Kantari-Mimoun, C. et al. Resolution of liver fibrosis requires myeloid cell-driven sinusoidal angiogenesis. Hepatology 61, 2042–2055 (2015).
Pellicoro, A. et al. Liver fibrosis and repair: immune regulation of wound healing in a solid organ. Nat. Rev. Immunol. 14, 181–194 (2014).
Su, S. et al. miR-142-5p and miR-130a-3p are regulated by IL-4 and IL-13 and control profibrogenic macrophage program. Nat. Commmun. 6, 8523 (2015).
Calvente, C. J. et al. Specific hepatic delivery of procollagen α1(I) small interfering RNA in lipid-like nanoparticles resolves liver fibrosis. Hepatology 62, 1285–1297 (2015).
Torok, N. J. et al. Strategies and endpoints of antifibrotic drug trials: summary and recommendations from the AASLD Emerging Trends Conference, Chicago, June 2014. Hepatology 62, 627–634 (2015).
Bajaj, J. S. et al. Salivary microbiota reflects changes in gut microbiota in cirrhosis with hepatic encephalopathy. Hepatology 62, 1260–1271 (2015).
Bajaj, J. S., Betrapally, N. S. & Gillevet, P. M. Decompensated cirrhosis and microbiome interpretation. Nature 525, E1–E3 (2015).
Szabo, G. Gut–liver axis in alcoholic liver disease. Gastroenterology 148, 30–36 (2015).
Karimi-Shah, B. A. & Chowdhury, B. A. Forced vital capacity in idiopathic pulmonary fibrosis — FDA review of pirfenidone and nintedanib. N. Engl. J. Med. 372, 1189–1191 (2015).
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K.P. is co-founder and minority shareholder in BiOrion Technologies. The antifibrotic compounds developed by BiOrion Technologies are not the subject of this Year-in-Review and are not mentioned in any other way in the article.
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Poelstra, K. Crucial steps towards an effective treatment. Nat Rev Gastroenterol Hepatol 13, 67–68 (2016). https://doi.org/10.1038/nrgastro.2015.224
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DOI: https://doi.org/10.1038/nrgastro.2015.224
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