Parties d'ouvrages collectifs (4)

  1. 1. Braet, F., Luo, D., Spector, I., Vermijlen, D., & Wisse, E. (2001). Endothelial and pit cells. In I. Arias, J. L. Boyer, F. Chisari, N. Fausto, D. Schachter, & D. Shafritz (Eds.), The liver: Biology and Pathobiology (4 ed., pp. 437-453). Philadelphia: Lippincott Williams & Wilkins.
  2. 2. Wisse, E., Braet, F., Luo, D., Vermijlen, D., Eddouks, M., Empsen, C., Spapen, H., & De Zanger, R. (1999). Sinusoidal liver cells. In Oxford Textbook of Clinical Hepatology (pp. 33-49). Oxford University Press.
  3. 3. Wisse, E., Braet, F., Luo, D., Vermijlen, D., Eddouks, M., Konstandoulaki, M., Empsen, C., & De Zanger, R. (1999). Endothelial cells of the hepatic sinusoids: A review. In K. Tanikawa & T. Ueno (Eds.), Liver Diseases and Hepatic Sinusoidal Cells (pp. 17-55). Springer-Verlag, Tokyo.
  4. 4. Wisse, E., Braet, F., Luo, D., Jans, D., Vermijlen, D., Kanellopoulou, C., Spapen, H., & De Zanger, R. (1997). On the tumoricide function of pit cells - the NK cells of the liver. In F. Vidal-Vanaclocha (Ed.), Functional heterogeneity of liver tissue (pp. 207-235). Heidelberg: Springer-Verlag.
  5.   Articles dans des revues avec comité de lecture (68)

  6. 1. Leong, J. Y., McGovern, N., Mishra, A., Wasser, M., Kumar, P., Tay, S. H., Nur Hazirah, S., Yeo, J. G., Tan, X. Q., Sutamam, N., Azman, F. N., Chua, C. J. H., Chen, P. Z., Ally, F., Dutertre, C. A., Ramakrishna, L., Poh, S. L., Xie, L., Fan, Y., Donner, C., Papadopoulou, M., Vermijlen, D., Arkachaisri, T., Chan, J. K. Y., Ginhoux, F., & Albani, S. (2025). Epigenetic instability and hypofunctionality of fetal Tregs allow a permissive regulatory environment for T effector memory maturation. Proceedings of the National Academy of Sciences of the United States of America, 122(30), e2506673122. doi:10.1073/pnas.2506673122
  7. 2. Tafesse, Y. M., Köhler, A., Sánchez Sánchez, G., Brito Rodrigues, P., Verce, M., Vitsos, P., Verdebout, I., Rezwani, M., Papadopoulou, M., Everard, A., Flamand, V., & Vermijlen, D. (2025). Maternal Administration of Probiotics Augments IL17‐Committed γδ T Cells in the Newborn Lung. European Journal of Immunology, 55(4). doi:10.1002/eji.202451051
  8. 3. Yang, B., Piedfort, O., Sánchez Sánchez, G., Lavergne, A., Gong, M., Peng, G., Madrigal, A., Petrellis, G., Katsandegwaza, B., Rodriguez, L. R., Balthazar, A., Meyer, S. J., Van Isterdael, G., Van Duyse, J., Andris, F., Bai, Q., Marichal, T., Machiels, B., Nitschke, L., Najafabadi, H. S., King, I. L., Vermijlen, D., & Dewals, B. G. (2025). IL-4 induces CD22 expression to restrain the effector program of virtual memory T cells. Science immunology, 10(104), eadk4841. doi:10.1126/sciimmunol.adk4841
  9. 4. Billiet, L., Jansen, H., Pille, M., Boehme, L., Sánchez Sánchez, G., De Cock, L., Goetgeluk, G., Pascal, E., De Munter, S., Deseins, L., Ingels, J., Michiels, T., De Vos, R., Zolfaghari, A., Vandamme, N., Roels, J., Kerre, T., Dmitriev, R. R., Taghon, T., Vermijlen, D., & Vandekerckhove, B. (2024). ThymoSpheres culture: A model to study human polyclonal unconventional T cells. European Journal of Immunology, e2451265. doi:10.1002/eji.202451265
  10. 5. Gong, M., Myster, F., Azouz, A., Sánchez Sánchez, G., Li, S., Charloteaux, B., Yang, B., Nichols, J., Lefevre, L., Javaux, J., Leemans, S., Nivelles, O., van Campe, W., Roels, S., Mostin, L., van den Berg, T., Davison, A. J., Gillet, L., Connelley, T., Vermijlen, D., Goriely, S., Vanderplasschen, A., & Dewals, B. G. (2024). Unraveling clonal CD8 T cell expansion and identification of essential factors in γ-herpesvirus-induced lymphomagenesis. Proceedings of the National Academy of Sciences of the United States of America, 121(32), e2404536121. doi:10.1073/pnas.2404536121
  11. 6. Yared, N., Papadopoulou, M., Barennes, P., Pham, H. P., Quiniou, V., Netzer, S., Kaminski, H., Burguet, L., Demeste, A., Colas, P., Mora-Charrot, L., Rousseau, B., Izotte, J., Zouine, A., Gauthereau, X., Vermijlen, D., Déchanet-Merville, J., & Capone, M. (2024). Long-lived central memory γδ T cells confer protection against murine cytomegalovirus reinfection. P L o S Pathogens, 20(7), e1010785. doi:10.1371/journal.ppat.1010785
  12. 7. Giannoni, E., Sánchez Sánchez, G., Verdebout, I., Papadopoulou, M., Rezwani, M., Ahmed, R., Ladell, K., Miners, K. L., McLaren, J. J., Fraser, D. J., Price, D. A., Eberl, M., Swiss Pediatric Sepsis Study,, Agyeman, P. K. A., Schlapbach, L. J., & Vermijlen, D. (2024). Sepsis shapes the human γδ TCR repertoire in an age- and pathogen-dependent manner. European Journal of Immunology, e2451190. doi:10.1002/eji.202451190
  13. 8. Sánchez Sánchez, G., Emmrich, S., Georga, M., Papadaki, A., Kossida, S., Seluanov, A., Gorbunova, V., & Vermijlen, D. (2024). Invariant γδTCR natural killer-like effector T cells in the naked mole-rat. Nature communications, 15(1), 4248. doi:10.1038/s41467-024-48652-z

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