Aureli, M., Schiumarini, D., Loberto, N., Bassi, R., Tamanini, A., Mancini, G., ... & Sonnino, S. (2016). Unravelling the role of sphingolipids in cystic fibrosis lung disease. Chemistry and Physics of Lipids, 200, 94-103. https://doi.org/10.1016/j.chemphyslip.2016.08.002
Bahri, S., Refini, R. M., d'Alessandro, M., Bergantini, L., Cameli, P., Vantaggiato, L., Bini, L., & Landi, C. (2017). The efficacy of plant extract and bioactive compounds in the treatment of pulmonary fibrosis. Biomedicine & Pharmacotherapy, 93, 666-673. https://doi.org/10.1016/j.biopha.2017.06.052
Bardin, P., Marchal-Duval, E., Sonneville, F., Blouquit-Laye, S., Rousselet, N., Le Rouzic, P., ... & Tabary, O. (2018). Small RNA and transcriptome sequencing reveal the role of miR-199a-3p in inflammatory processes in cystic fibrosis airways. Journal of Pathology, 245(4), 410-420.
https://doi.org/10.1002/path.5095
Bargagli, E., Refini, R. M., d'Alessandro, M., Bergantini, L., Cameli, P., Vantaggiato, L., Bini, L., & Landi, C. (2020). Metabolic dysregulation in idiopathic pulmonary fibrosis. International Journal of Molecular Sciences, 21(16), 5663. https://doi.org/10.3390/ijms21165663
Becker, K. A., Riethmüller, J., Zhang, Y., & Gulbins, E. (2010). The role of sphingolipids and ceramide in pulmonary inflammation in cystic fibrosis. Open Respiratory Medicine Journal, 4, 39-47.
https://doi.org/10.2174/1874306401004010039
Bonfield, T. L., Panuska, J. R., Konstan, M. W., Hilliard, K. A., Hilliard, J. B., Ghnaim, H., et al. (1995). Inflammatory cytokines in cystic fibrosis lungs. American Journal of Respiratory and Critical Care Medicine, 152, 2111-2118. https://doi.org/10.1164/ajrccm.152.6.8520783
Bruscia, E. M., Zhang, P.-X., Ferreira, E., Caputo, C., Emerson, J. W., Tuck, D., et al. (2009). Macrophages directly contribute to the exaggerated inflammatory response in cystic fibrosis transmembrane conductance regulator−/− mice. American Journal of Respiratory Cell and Molecular Biology, 40, 295-304.
https://doi.org/10.1165/rcmb.2008-0170OC
Chang, H., Meng, H. Y., Bai, W. F., & Meng, Q. G. (2021). A metabolomic approach to elucidate the inhibitory effects of baicalin in pulmonary fibrosis. Pharmaceutical Biology, 59(1), 1014-1023.
https://doi.org/10.1080/13880209.2021.1950192
Dechecchi, M. C., Nicolis, E., Norez, C., Bezzerri, V., Borgatti, M., Mancini, I., et al. (2008). Anti-inflammatory effect of miglustat in bronchial epithelial cells. Journal of Cystic Fibrosis, 7, 555-565.
https://doi.org/10.1016/j.jcf.2008.06.002
Dechecchi, M. C., Nicolis, E., Norez, C., Bezzerri, V., Borgatti, M., Mancini, I., ... & Tabary, O. (2011). Modulators of sphingolipid metabolism reduce lung inflammation in cystic fibrosis. American Journal of Respiratory Cell and Molecular Biology, 45(6), 825-833. https://doi.org/10.1165/rcmb.2010-0457OC
Fischer, R., Schwarz, C., Weiser, R., et al. (2022). Evaluating the alginate oligosaccharide (OligoG) as a therapy for Burkholderia cepacia complex cystic fibrosis lung infection. Journal of Cystic Fibrosis, 21, 821-829. https://doi.org/10.1016/j.jcf.2022.01.003
Ghorbani, P., Santhakumar, P., Hu, Q., Djiadeu, P., Wolever, T. M. S., Palaniyar, N., & Grasemann, H. (2015). Short-chain fatty acids affect cystic fibrosis airway inflammation and bacterial growth. European Respiratory Journal, 46(4), 1033-1045. https://doi.org/10.1183/09031936.00143614
Gramegna, A., Magnoni, C., Premuda, C., Alicandro, G., Akkerman, O., Amorim, A., ... & Blasi, F. (2026). Determinants of early Elexacaftor-Tezacaftor-Ivacaor use in adults with cystic fibrosis and preserved lung function: insights from a European multicenter survey. Journal of Cystic Fibrosis. Advance online publication. https://doi.org/10.1016/j.jcf.2026.03.005
Harwood, K. H., McQuade, R. M., Jarnicki, A., & Schneider-Futschik, E. K. (2021). Anti-inflammatory influences of cystic fibrosis transmembrane conductance regulator drugs on lung inflammation in cystic fibrosis. International Journal of Molecular Sciences, 22(14), 7606. https://doi.org/10.3390/ijms22147606
Horati, H., Janssens, H. M., Margaroli, C., Veltman, M., Stolarczyk, M., Kilgore, M. B., ... & Scholte, B. J. (2020). Airway profile of bioactive lipids predicts early progression of lung disease in cystic fibrosis. Journal of Cystic Fibrosis, 19(6), 902-909. https://doi.org/10.1016/j.jcf.2020.01.010
Hou, S., Yue, Q., Hou, X., & Wu, Q. (2025). Targeting the aryl hydrocarbon receptor: The potential of indole compounds in the treatment of cystic fibrosis. International Journal of Molecular Sciences, 26(20), 9876. https://doi.org/10.3390/ijms26209876
Hunter, R. C., Klepac-Ceraj, V., Lorenzi, M. M., Grotzinger, H., Martin, T. R., & Newman, D. K. (2012). Phenazine content in the cystic fibrosis respiratory tract negatively correlates with lung function and microbial complexity. American Journal of Respiratory Cell and Molecular Biology, 47, 738-745.
https://doi.org/10.1165/rcmb.2012-0088OC
Jarosz-Griffiths, H. H., Scambler, T., Wong, C. H., Lara-Reyna, S., Holbrook, J., Martinon, F., et al. (2020). Different CFTR modulator combinations downregulate inflammation differently in cystic fibrosis. eLife, 9.
https://doi.org/10.7554/eLife.54556.sa2
Khan, T. Z., Wagener, J. S., Bost, T., Martinez, J., Accurso, F. J., & Riches, D. W. (1995). Early pulmonary inflammation in infants with cystic fibrosis. American Journal of Respiratory and Critical Care Medicine, 151, 1075-1082. https://doi.org/10.1164/ajrccm/151.4.1075
Konstan, M. W., Hilliard, K. A., Norvell, T. M., & Berger, M. (1994). Bronchoalveolar lavage findings in cystic fibrosis patients with stable, clinically mild lung disease suggest ongoing infection and inflammation. American Journal of Respiratory and Critical Care Medicine, 150, 448-454. https://doi.org/10.1164/ajrccm.150.2.8049828
Lévêque, M., Le Jeune, A., Jouneau, S., Jan, S., & Catheline, D. (2017). Alterations in lipid membrane composition in CF macrophage may play a role in chronic infections in CF patients. Journal of Cystic Fibrosis, 16(4), 443-453. https://doi.org/10.1016/j.jcf.2016.10.011
Luo, J., Luo, J., Fang, Z., Fu, Y., & Xu, B. (2025). Insights into effects of natural bioactive components on inflammatory diseases in respiratory tract. Phytotherapy Research. Advance online publication. https://doi.org/10.1002/ptr.8367
Makam, M., Diaz, D., Laval, J., Gernez, Y., Conrad, C. K., Dunn, C. E., ... & Tirouvanziam, R. (2009). Activation of critical, host-induced, metabolic and stress pathways marks neutrophil entry into cystic fibrosis lungs. Proceedings of the National Academy of Sciences, 106(14), 5779-5783. https://doi.org/10.1073/pnas.0813410106
Marsh, R., Tricker, J. M., Delhaes, L., Bomberger,J. M., & van der Gast, C. (2026). The gut microbiome: Recent findings and future opportunities in cystic fibrosis. Journal of Cystic Fibrosis. https://doi.org/10.1016/j.jcf.2026.05.003
Meoli, A., Eickmeier, O., Pisi, G., Fainardi, V., Zielen, S., & Esposito, S. (2022). Impact of CFTR modulators on the impaired function of phagocytes in cystic fibrosis lung disease. International Journal of Molecular Sciences, 23(20), 12421. https://doi.org/10.3390/ijms232012421
Mitri, C., Xu, Z., Bardin, P., Corvol, H., Touqui, L., & Tabary, O. (2020). Novel anti-inflammatory approaches for cystic fibrosis lung disease: Identification of molecular targets and design of innovative therapies. Frontiers in Pharmacology, 11, 1096. https://doi.org/10.3389/fphar.2020.01096
Pailhoriès, H., Velo-Suarez, L., Moalic, Y., et al. (2026). A disrupted microbial network and an ecological shift towards anaerobes in NTM-infected cystic fibrosis patients. Journal of Cystic Fibrosis.
https://doi.org/10.1016/j.jcf.2026.04.005
Papa, R., Garzoli, S., Vrenna, G., Sabatino, M., Sapienza, F., Relucenti, M., ... & Ragno, R. (2020). Essential oils biofilm modulation activity, chemical and machine learning analysis-Application on Staphylococcus aureus isolates from cystic fibrosis patients. International Journal of Molecular Sciences, 21(23), 9258.
https://doi.org/10.3390/ijms21239258
Scholte, B. J., Horati, H., Veltman, M., Vreeken, R. J., Garratt, L. W., Tiddens, H. A., ... & Stick, S. (2019). Oxidative stress and abnormal bioactive lipids in early cystic fibrosis lung disease. Journal of Cystic Fibrosis, 18(6), 781–789. https://doi.org/10.1016/j.jcf.2019.04.011
Seidl, E., Licht, J. C., Slingers, G., van Koningsbruggen-Rietschel, S., van der Gast, C., Fragoso, C., ... & Grasemann, H. (2026). CFTR modulator therapy with ETI does not significantly alter eNose-derived VOC breath profiles in children with CF. Journal of Cystic Fibrosis. Advance online publication. https://doi.org/10.1016/j.jcf.2026.03.014
Snowball, J., Salem, V., Wu, M., & Blackman, S. M. (2026). Perspectives in cystic fibrosis related diabetes (CFRD) research. Journal of Cystic Fibrosis. Advance online publication.
Taccetti, G., Francalanci, M., Pizzamiglio, G., et al. (2021). Cystic fibrosis: Recent insights into inhaled antibiotic treatment and future perspectives. Antibiotics, 10, 338. https://doi.org/10.3390/antibiotics10030338
Thavamani, A., Salem, I., Sferra, T. J., & Sankararaman, S. (2021). Impact of altered gut microbiota and its metabolites in cystic fibrosis. Metabolites, 11(2), 123. https://doi.org/10.3390/metabo11020123
Trandafir, L. M., Frasinariu, O. E., Tarca, E., Butnariu, L. I., Leon Constantin, M. M., Moscalu, M., ... & Moisa, S. M. (2023). Can bioactive food substances contribute to cystic fibrosis-related cardiovascular disease prevention?. Nutrients, 15(2), 314. https://doi.org/10.3390/nu15020314
Untersmayr, E., Stafflinger-Fürst, E., Heiden, D., Diesner, S. C., Japtok, L., Kleuser, B., ... & Kozelsky-Scholte, L. (2020). Plasma S1P levels are influenced by CFTR function and correlate with clinical symptoms in adult CF patients. Nutrients, 12(3), 765. https://doi.org/10.3390/nu12030765
Yan, F., Wen, Z., Wang, R., Luo, W., Du, Y., Wang, W., & Chen, X. (2017). Identification of the lipid biomarkers from plasma in idiopathic pulmonary fibrosis by Lipidomics. BMC pulmonary medicine, 17(1), 174. https://doi.org/10.1186/s12890-017-0513-4