The DOI matches its Crossref record; 98 of the 99 references it cites were found in a registry or an index.
Fate-Mapping of GM-CSF Expression Identifies a Discrete Subset of Inflammation-Driving T Helper Cells Regulated by Cytokines IL-23 and IL-1β
Open accessAbstract
Pathogenic lymphocytes initiate the development of chronic inflammatory diseases. The cytokine granulocyte-macrophage colony-stimulating factor (GM-CSF) (encoded by Csf2) is a key communicator between pathogenic lymphocytes and tissue-invading inflammatory phagocytes. However, the molecular properties of GM-CSF-producing cells and the mode of Csf2 regulation in vivo remain unclear. To systematically study and manipulate GM-CSF+ cells and their progeny in vivo, we generated a fate-map and reporter of GM-CSF expression mouse strain (FROG). We mapped the phenotypic and functional profile of auto-aggressive T helper (Th) cells during neuroinflammation and identified the signature and pathogenic memory of a discrete encephalitogenic Th subset. These cells required interleukin-23 receptor (IL-23R) and IL-1R but not IL-6R signaling for their maintenance and pathogenicity. Specific ablation of this subset interrupted the inflammatory cascade, despite the unperturbed tissue accumulation of other Th subsets (e.g., Th1 and Th17), highlighting that GM-CSF expression not only marks pathogenic Th cells, but that this subset mediates immunopathology and tissue destruction.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The text we found for this paper looks like another document, so the self-check wasn’t run.
Citations
Cites
Trimmomatic: a flexible trimmer for Illumina sequence data
Bolger, A. M., Lohse, M., & Usadel, B. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu170 · Cited by 65,548
Fast gapped-read alignment with Bowtie 2
Langmead, B., & Salzberg, S. L. (2012) · Nature Methods · doi:10.1038/nmeth.1923 · Cited by 56,400
(2008) · Journal of Machine Learning Research · Cited by 33,051
ggplot2: Elegant Graphics for Data Analysis
Ginestet, C. E. (2011) · Journal of the Royal Statistical Society Series A (Statistics in Society) · doi:10.1111/j.1467-985x.2010.00676_9.x · Cited by 14,511
ggplot2: Elegant Graphics for Data Analysis
Wickham, H. (2009) · doi:10.1007/978-0-387-98141-3 · Cited by 14,447
A robust and high-throughput Cre reporting and characterization system for the whole mouse brain
Madisen, L., Zwingman, T. A., Sunkin, S. M., Oh, S. W., Zariwala, H. A., Gu, H., Ng, L. L., Palmiter, R. D., Hawrylycz, M. J., Jones, A. R., et al. (2010) · Nature Neuroscience · doi:10.1038/nn.2467 · Cited by 6,907
Buenrostro, J. D., Giresi, P. G., Zaba, L. C., Chang, H. Y., & Greenleaf, W. J. (2013) · Nature Methods · doi:10.1038/nmeth.2688 · Cited by 6,422
IL-23 drives a pathogenic T cell population that induces autoimmune inflammation
Langrish, C. L., Chen, Y., Blumenschein, W. M., Mattson, J., Basham, B., Sedgwick, J. D., McClanahan, T., Kastelein, R. A., & Cua, D. J. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20041257 · Cited by 4,099
Veldhoen, M., Hocking, R. J., Atkins, C. J., Locksley, R. M., & Stockinger, B. (2006) · Immunity · doi:10.1016/j.immuni.2006.01.001 · Cited by 3,605
Liao, Y., Smyth, G. K., & Shi, W. (2019) · Nucleic Acids Research · doi:10.1093/nar/gkz114 · Cited by 2,927
Cited by
Sorted by citations
Astrocyte Crosstalk in CNS Inflammation
Linnerbauer, M., Wheeler, M. A., & Quintana, F. J. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.012 · Cited by 989
Microglia: Immune and non-immune functions
Borst, K., Dumas, A. A., & Prinz, M. (2021) · Immunity · doi:10.1016/j.immuni.2021.09.014 · Cited by 804
Function and therapeutic value of astrocytes in neurological diseases
Lee, H.-G., Wheeler, M. A., & Quintana, F. J. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-022-00390-x · Cited by 662
Microglia and Central Nervous System–Associated Macrophages—From Origin to Disease Modulation
Prinz, M., Masuda, T., Wheeler, M. A., & Quintana, F. J. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-093019-110159 · Cited by 584
Establishment and Maintenance of the Macrophage Niche
Guilliams, M., Thierry, G. R., Bonnardel, J., & Bajenoff, M. (2020) · Immunity · doi:10.1016/j.immuni.2020.02.015 · Cited by 512
Serum Amyloid A Proteins Induce Pathogenic Th17 Cells and Promote Inflammatory Disease
Lee, J., Hall, J. A., Kroehling, L., Wu, L., Najar, T. A., Nguyen, H. H., Lin, W.-Y., Yeung, S. T., Silva, H. M., Li, D., et al. (2019) · Cell · doi:10.1016/j.cell.2019.11.026 · Cited by 476
Microglia Require CD4 T Cells to Complete the Fetal-to-Adult Transition
Pasciuto, E., Burton, O. T., Roca, C. P., Lagou, V., Rajan, W. D., Theys, T., Mancuso, R., Tito, R. Y., Kouser, L., Callaerts-Vegh, Z., et al. (2020) · Cell · doi:10.1016/j.cell.2020.06.026 · Cited by 368
Astrocytic interleukin-3 programs microglia and limits Alzheimer’s disease
McAlpine, C. S., Park, J., Griciuc, A., Kim, E., Choi, S. H., Iwamoto, Y., Kiss, M. G., Christie, K. A., Vinegoni, C., Poller, W. C., et al. (2021) · Nature · doi:10.1038/s41586-021-03734-6 · Cited by 322
Hamilton, J. A. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190945 · Cited by 324
TH17 cell heterogeneity and its role in tissue inflammation
Schnell, A., Littman, D. R., & Kuchroo, V. K. (2023) · Nature Immunology · doi:10.1038/s41590-022-01387-9 · Cited by 286
Stem-like intestinal Th17 cells give rise to pathogenic effector T cells during autoimmunity
Schnell, A., Huang, L., Singer, M., Singaraju, A., Barilla, R. M., Regan, B. M. L., Bollhagen, A., Thakore, P. I., Dionne, D., Delorey, T. M., et al. (2021) · Cell · doi:10.1016/j.cell.2021.11.018 · Cited by 268
Interleukin-17 in chronic inflammatory neurological diseases
Milovanovic, J., Arsenijevic, A., Stojanovic, B., Kanjevac, T., Arsenijevic, D., Radosavljevic, G., Milovanovic, M., & Arsenijevic, N. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00947 · Cited by 250
GM-CSF-based treatments in COVID-19: reconciling opposing therapeutic approaches
Lang, F. M., Lee, M.-C., Teijaro, J. R., Becher, B., & Hamilton, J. A. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-020-0357-7 · Cited by 237
Self-citationMultiple sclerosis: Neuroimmune crosstalk and therapeutic targeting
Charabati, M., Wheeler, M. A., Weiner, H. L., & Quintana, F. J. (2023) · Cell · doi:10.1016/j.cell.2023.03.008 · Cited by 242
Microglia and monocytes in inflammatory CNS disease: integrating phenotype and function
Spiteri, A. G., Wishart, C. L., Pamphlett, R., Locatelli, G., & King, N. J. C. (2022) · Acta Neuropathologica · doi:10.1007/s00401-021-02384-2 · Cited by 216
“Indeed, GM-CSF signalling is thought to induce a characteristic transcriptional signature in monocytes that is sufficient to drive disease onset [67, 190].”
BackgroundGM-CSF and CXCR4 define a T helper cell signature in multiple sclerosis
Galli, E., Hartmann, F. J., Schreiner, B., Ingelfinger, F., Arvaniti, E., Diebold, M., Mrdjen, D., van der Meer, F., Krieg, C., Nimer, F. A., et al. (2019) · Nature Medicine · doi:10.1038/s41591-019-0521-4 · Cited by 197
Self-citationAlveolar macrophages rely on GM-CSF from alveolar epithelial type 2 cells before and after birth
Gschwend, J., Sherman, S., Ridder, F., Feng, X., Liang, H.-E., Locksley, R. M., Becher, B., & Schneider, C. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20210745 · Cited by 185
Self-citationRepositioning TH cell polarization from single cytokines to complex help
Tuzlak, S., Dejean, A. S., Iannacone, M., Quintana, F. J., Waisman, A., Ginhoux, F., Korn, T., & Becher, B. (2021) · Nature Immunology · doi:10.1038/s41590-021-01009-w · Cited by 171
Self-citationWhen encephalitogenic T cells collaborate with microglia in multiple sclerosis
Dong, Y., & Yong, V. W. (2019) · Nature Reviews Neurology · doi:10.1038/s41582-019-0253-6 · Cited by 169
Amorim, A., De Feo, D., Friebel, E., Ingelfinger, F., Anderfuhren, C. D., Krishnarajah, S., Andreadou, M., Welsh, C. A., Liu, Z., Ginhoux, F., et al. (2022) · Nature Immunology · doi:10.1038/s41590-021-01117-7 · Cited by 140
Self-citationKamma, E., Lasisi, W. O., Libner, C. D., Ng, H. S., & Plemel, J. R. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02408-y · Cited by 157
Bystander CD4+ T cells: crossroads between innate and adaptive immunity
Lee, H., Cho, M.-J., & Choi, J. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-00486-7 · Cited by 157
Pathogenic T cell cytokines in multiple sclerosis
Wagner, C. A., Roqué, P. J., & Goverman, J. M. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20190460 · Cited by 132
Molecular control of pathogenic Th17 cells in autoimmune diseases
Wu, B., & Wan, Y. Y. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.106187 · Cited by 128
Kuo, P., Weng, W., Scofield, B. A., Paraiso, H. C., Brown, D. A., Wang, P., Yu, I.-C. I., & Yen, J.-H. J. (2020) · Journal of Neuroinflammation · doi:10.1186/s12974-020-01768-7 · Cited by 113
Cellular and molecular pathophysiology in the progression of Parkinson’s disease
Zaman, V., Shields, D. C., Shams, R., Drasites, K. P., Matzelle, D. D., Haque, A., & Banik, N. L. (2021) · Metabolic Brain Disease · doi:10.1007/s11011-021-00689-5 · Cited by 119
Th17 cells and inflammation in neurological disorders: Possible mechanisms of action
Shi, Y., Wei, B., Li, L., Wang, B., & Sun, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.932152 · Cited by 108
Casella, G., Rasouli, J., Boehm, A., Zhang, W., Xiao, D., Ishikawa, L. L. W., Thomé, R., Li, X., Hwang, D., Porazzi, P., et al. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aba0599 · Cited by 105
TNF plays a crucial role in inflammation by signaling via T cell TNFR2
Alam, M. S., Otsuka, S., Wong, N. W., Abbasi, A. J., Gaida, M. M., Fan, Y., Meerzaman, D. M., & Ashwell, J. D. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2109972118 · Cited by 109
Bidirectional Communication Between Microglia and Astrocytes in Neuroinflammation
Bhusal, A., Afridi, R., Lee, W., & Suk, K. (2022) · Current Neuropharmacology · doi:10.2174/1570159x21666221129121715 · Cited by 113
The role of Th17 cells/IL-17A in AD, PD, ALS and the strategic therapy targeting on IL-17A
Fu, J., Huang, Y., Bao, T., Liu, C., Liu, X., & Chen, X. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02446-6 · Cited by 103
Decoding IL-23 Signaling Cascade for New Therapeutic Opportunities
Pastor-Fernández, G., Mariblanca, I. R., & Navarro, M. N. (2020) · Cells · doi:10.3390/cells9092044 · Cited by 102
NK cell–derived GM-CSF potentiates inflammatory arthritis and is negatively regulated by CIS
Louis, C., Souza-Fonseca-Guimarães, F., Yang, Y., D'Silva, D. B., Kratina, T., Dagley, L., Hediyeh-zadeh, S., Rautela, J., Masters, S., Davis, M., et al. (2020) · Journal of Experimental Medicine · doi:10.1084/jem.20191421 · Cited by 87
Targeting interleukin-17 in chronic inflammatory disease: A clinical perspective
Zwicky, P., Unger, S., & Becher, B. (2020) · Journal of Experimental Medicine · doi:10.1084/jem.20191123 · Cited by 91
Self-citationJahromi, N. H., Marchetti, L., Moalli, F., Duc, D., Basso, C., Tardent, H., Kaba, E., Deutsch, U., Pot, C., Sallusto, F., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2019.03056 · Cited by 93
Pawlak, M., Ho, A. W., & Kuchroo, V. K. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2020.09.001 · Cited by 93
Natural killer cells in inflammatory autoimmune diseases
Yang, Y., Day, J. A., Souza-Fonseca-Guimarães, F., Wicks, I. P., & Louis, C. (2021) · Clinical & Translational Immunology · doi:10.1002/cti2.1250 · Cited by 80
Th17 cell pathogenicity in autoimmune disease
Park, E., & Ciofani, M. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01535-9 · Cited by 75
Michel, L., Grasmuck, C., Charabati, M., Lécuyer, M., Zandee, S., Dhaeze, T., Alvarez, J. I., Li, R., Larouche, S., Bourbonnière, L., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aaw0475 · Cited by 72
The CNS mononuclear phagocyte system in health and disease
Mundt, S., Greter, M., & Becher, B. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.005 · Cited by 68
Self-citationEpigenetic Regulation of T Cell Memory: Recalling Therapeutic Implications
Tough, D. F., Rioja, I., Modis, L. K., & Prinjha, R. K. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.11.008 · Cited by 67
Angelou, C. C., Wells, A. C., Vijayaraghavan, J., Dougan, C. E., Lawlor, R. G., Iverson, E., Lazarevic, V., Kimura, M. Y., Peyton, S. R., Minter, L. M., et al. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2019.03125 · Cited by 63
Targeting GM-CSF in inflammatory and autoimmune disorders
Achuthan, A. A., Lee, M.-C., & Hamilton, J. A. (2021) · Seminars in Immunology · doi:10.1016/j.smim.2021.101523 · Cited by 66
The neuroimmune connectome in health and disease
Wheeler, M. A., & Quintana, F. J. (2025) · Nature · doi:10.1038/s41586-024-08474-x · Cited by 71
GM-CSF: Master regulator of the T cell-phagocyte interface during inflammation
Ingelfinger, F., De Feo, D., & Becher, B. (2021) · Seminars in Immunology · doi:10.1016/j.smim.2021.101518 · Cited by 61
Self-citationChemokine-Driven Migration of Pro-Inflammatory CD4+ T Cells in CNS Autoimmune Disease
Heng, A. H. S., Han, C. W., Abbott, C. A., McColl, S. R., & Comerford, I. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.817473 · Cited by 61
Rasouli, J., Casella, G., Yoshimura, S., Zhang, W., Xiao, D., Garifallou, J., Gonzalez, M. V., Wiedeman, A., Kus, A., Mari, E. R., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.aba9953 · Cited by 57
Role of the CXCR6/CXCL16 axis in autoimmune diseases
Bao, N., Fu, B., Zhong, X., Jia, S., Ren, Z., Wang, H., Wang, W., Shi, H. R., Li, ., Ge, F., et al. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110530 · Cited by 58
Colony stimulating factors in the nervous system
Chiţu, V., Biundo, F., & Stanley, E. R. (2021) · Seminars in Immunology · doi:10.1016/j.smim.2021.101511 · Cited by 57
Aging weakens Th17 cell pathogenicity and ameliorates experimental autoimmune uveitis in mice
Li, H., Zhu, L., Wang, R., Xie, L., Ren, J., Ma, S., Zhang, W., Liu, X., Huang, Z., Chen, B., et al. (2021) · Protein & Cell · doi:10.1007/s13238-021-00882-3 · Cited by 53
Activation pathways that drive CD4 + T cells to break tolerance in autoimmune diseases*
Krovi, S. H., & Kuchroo, V. K. (2022) · Immunological Reviews · doi:10.1111/imr.13071 · Cited by 56
Hu, H., Li, H., Li, R., Liu, P., & Liu, H. (2024) · Journal of Translational Medicine · doi:10.1186/s12967-024-05450-x · Cited by 56
Induction of a colitogenic phenotype in Th1-like cells depends on interleukin-23 receptor signaling
Pawlak, M., DeTomaso, D., Schnell, A., Meyer zu Horste, G., Lee, Y., Nyman, J., Dionne, D., Regan, B. M. L., Singh, V., Delorey, T., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.08.007 · Cited by 49
Central Nervous System Macrophages in Health and Disease
Hove, H. V., Feo, D. D., Greter, M., & Becher, B. (2025) · Annual Review of Immunology · doi:10.1146/annurev-immunol-082423-041334 · Cited by 53
Self-citationThe role of iron metabolism in the pathogenesis and treatment of multiple sclerosis
Duarte-Silva, E., Meuth, S. G., & Peixoto, C. A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1137635 · Cited by 46
Lu, Y.-P., Chen, X., Liu, X., Shi, Y. P., Wei, Z., Feng, L., Jiang, Q., Ye, W., Sasaki, T., Fukunaga, K., et al. (2023) · Autophagy · doi:10.1080/15548627.2022.2162244 · Cited by 47
Innate and adaptive immune abnormalities underlying autoimmune diseases: the genetic connections
Chi, X., Huang, M., Tu, H., Zhang, B., Lin, X., Xu, H., Dong, C., & Hu, X. (2023) · Science China Life Sciences · doi:10.1007/s11427-021-2187-3 · Cited by 47
SerpinB1 controls encephalitogenic T helper cells in neuroinflammation
Hou, L., Rao, D. A., Yuki, K., Cooley, J., Henderson, L. A., Jonsson, A. H., Kaiserman, D., Gorman, M., Nigrovic, P. A., Bird, P. I., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1905762116 · Cited by 43
Self-citationTh17 Cells in Inflammatory Bowel Disease: An Update for the Clinician
Hou, G., & Bishu, S. (2020) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izz316 · Cited by 47
TH Cells and Cytokines in Encephalitogenic Disorders
Krishnarajah, S., & Becher, B. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.822919 · Cited by 49
Self-citationTatović, D., Marwaha, A., Taylor, P. N., Hanna, S. J., Carter, K., Cheung, W., Luzio, S. D., Dunseath, G. J., Hutchings, H. A., Holland, G., et al. (2024) · Nature Medicine · doi:10.1038/s41591-024-03115-2 · Cited by 53
B cells polarize pathogenic inflammatory T helper subsets through ICOSL-dependent glycolysis
Zeng, Q., Yuan, W., Lao, X., Chen, D., Huang, C.-X., Lin, Q., He, M. Y., Liao, Y., Zheng, L., Li, B., et al. (2020) · Science Advances · doi:10.1126/sciadv.abb6296 · Cited by 45
CXCR6-based immunotherapy in autoimmune, cancer and inflammatory infliction
Li, T., Pan, J., Chen, H., Fang, Y., & Sun, Y. (2022) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2022.03.012 · Cited by 39
Astrocytes and Microglia in Stress-Induced Neuroinflammation: The African Perspective
Olude, M. A., Mouihate, A., Mustapha, O. A., Farina, C., Quintana, F. J., & Olopade, J. O. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.795089 · Cited by 37
Zhang, C., Kang, J., Zhang, X., Zhang, Y., Huang, N., & Ning, B. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113500 · Cited by 40
Bhaskaran, S., Kumar, G., Thadathil, N., Piekarz, K. M., Mohammed, S., Domínguez-López, S., Qaisar, R., Walton, D. A., Brown, J. L., Murphy, A., et al. (2022) · Redox Biology · doi:10.1016/j.redox.2022.102550 · Cited by 36
Macrophage responses associated with COVID-19: A pharmacological perspective
Booz, G. W., Altara, R., Eid, A. H., Wehbe, Z., Fares, S. A., Zaraket, H., Habeichi, N. J., & Zouein, F. A. (2020) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2020.173547 · Cited by 38
The Role of Granulocyte-Macrophage Colony-Stimulating Factor in Murine Models of Multiple Sclerosis
Monaghan, K. L., & Wan, E. C. K. (2020) · Cells · doi:10.3390/cells9030611 · Cited by 35
Gil‐Pulido, J., Amézaga, N., Jorgacevic, I., Manthey, H. D., Rösch, M., Brand, T., Cidlinsky, P., Schäfer, S., Beilhack, A., Saliba, A., et al. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab359 · Cited by 36
Self-citationN’diaye, M., Brauner, S., Flytzani, S., Kular, L., Warnecke, A., Adzemovic, M. Z., Piket, E., Min, J.-H., Edwards, W., Mela, F., et al. (2019) · Journal of Clinical Investigation · doi:10.1172/jci125857 · Cited by 33
Chen, J., Martindale, J. L., Abdelmohsen, K., Kumar, G., Fortina, P. M., Gorospe, M., Rostami, A. M., & Yu, S. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1900769 · Cited by 34
The hedgehog pathway suppresses neuropathogenesis in CD4 T cell-driven inflammation
Benallegue, N., Kébir, H., Kapoor, R., Crockett, A. M., Li, C., Cheslow, L., Abdel-Hakeem, M. S., Gesualdi, J., Miller, M. C., Wherry, E. J., et al. (2021) · Brain · doi:10.1093/brain/awab083 · Cited by 31
Salvator, H., Cheng, A., Rosen, L. B., Williamson, P. R., Bennett, J. E., Kashyap, A. K., Ding, L., Kwon-Chung, K. J., Namkoong, H., Zerbe, C. S., et al. (2022) · Respiratory Research · doi:10.1186/s12931-022-02103-9 · Cited by 33
Targeting Th17 cells: a promising strategy to treat oral mucosal inflammatory diseases
Wang, Y., Xue, N., Wang, Z., Zeng, X. Y., Ji, N., & Chen, Q. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1236856 · Cited by 32
Musella, A., Fresegna, D., Rizzo, F. R., Gentile, A., Vito, F. D., Caioli, S., Guadalupi, L., Bruno, A., Dolcetti, E., Buttari, F., et al. (2020) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2020.1709823 · Cited by 33
Laouarem, Y., Kassoussi, A., Zahaf, A., Hutteau-Hamel, T., Mellouk, A., Bobé, P., Mattern, C., Schumacher, M., & Traiffort, É. (2021) · Glia · doi:10.1002/glia.23967 · Cited by 31
Tetramerization of STAT5 promotes autoimmune-mediated neuroinflammation
Monaghan, K. L., Aesoph, D., Ammer, A. G., Zheng, W., Rahimpour, S., Farris, B. Y., Spinner, C. A., Li, P., Lin, J., Yu, Z., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2116256118 · Cited by 31
Shen, M.-Y., Di, Y., Wang, X., Tian, F.-X., Zhang, M.-F., Qian, F., Jiang, B., Zhou, X., & Zhou, L. (2023) · Pharmaceutical Biology · doi:10.1080/13880209.2023.2173248 · Cited by 30
Paust, H., Song, N., Feo, D. D., Asada, N., Tuzlak, S., Zhao, Y., Riedel, J.-H., Hellmig, M., Sivayoganathan, A., Peters, A., et al. (2023) · Science Translational Medicine · doi:10.1126/scitranslmed.add6137 · Cited by 30
Self-citationGM-CSF: Orchestrating the Pulmonary Response to Infection
McCormick, T. S., Hejal, R. B., Leal, L. O., & Ghannoum, M. A. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.735443 · Cited by 31
Mills, K. A. M., Westermann, F., Espinosa, V., Rosiek, E., Desai, J. V., Aufiero, M. A., Guo, Y., Liu, F. L., Mitchell, K. A., Tuzlak, S., et al. (2025) · Science Immunology · doi:10.1126/sciimmunol.adr0547 · Cited by 30
Self-citationInterleukin 23 receptor: Expression and regulation in immune cells
Mezghiche, I., Yahia‐Cherbal, H., Rogge, L., & Bianchi, E. (2023) · European Journal of Immunology · doi:10.1002/eji.202250348 · Cited by 32
Aliyu, M., Zohora, F. T., Ceylan, A., Hossain, F., Yazdani, R., & Azizi, G. (2024) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923973.2024.2330642 · Cited by 28
Shen, M.-Y., Wang, X., Di, Y., Zhang, M.-F., Tian, F.-X., Qian, F., Jiang, B., & Zhou, L. (2022) · Immunopharmacology and Immunotoxicology · doi:10.1080/08923973.2022.2086139 · Cited by 27
CD4 + T cells require Ikaros to inhibit their differentiation toward a pathogenic cell fate
Bernardi, C., Maurer, G., Ye, T., Marchal, P., Jost, B., Wissler, M., Maurer, U., Kastner, P., Chan, S. H., & Charvet, C. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2023172118 · Cited by 25
Berek, K., Bauer, A., Rudzki, D., Auer, M., Barket, R., Zinganell, A., Lerch, M., Hofer, L., Grams, A. E., Poskaite, P., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1200146 · Cited by 25
Neuroinflammation: Extinguishing a blaze of T cells
Benallegue, N., Kébir, H., & Alvarez, J. I. (2022) · Immunological Reviews · doi:10.1111/imr.13122 · Cited by 25
Weng, W., Kuo, P., Brown, D. A., Scofield, B. A., Furnas, D., Paraiso, H. C., Wang, P., Yu, I.-C. I., & Yen, J.-H. J. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02143-w · Cited by 24
Cholinergic control of Th17 cell pathogenicity in experimental autoimmune encephalomyelitis
Nechanitzky, R., Nechanitzky, D., Ramachandran, P., Duncan, G. S., Zheng, C., Göbl, C., Gill, K. T., Haight, J., Wakeham, A. C., Snow, B. E., et al. (2022) · Cell Death and Differentiation · doi:10.1038/s41418-022-01092-y · Cited by 23
Polonio, C. M., de Freitas, C. L., de Oliveira, M. G., Rossato, C., Brandão, W. N., Zanluqui, N. G., de Oliveira, L. G., Mimura, L. A. N., Silva, M. B. B., Calich, V. L. G., et al. (2021) · Clinical Science · doi:10.1042/cs20201544 · Cited by 20
Astrocytes in ischemic stroke: Crosstalk in central nervous system and therapeutic potential
Liu, J., Guo, Y., Zhang, Y., Zhao, X., Fu, R., Hua, S., & Xu, S. (2023) · Neuropathology · doi:10.1111/neup.12928 · Cited by 21
Li, H., Zhu, L., Wang, R., Xie, L.-H., Chen, Y., Duan, R.-P., Liu, X.-X., Huang, Z.-H., Chen, B.-Y., Li, Z.-H., et al. (2021) · Investigative Ophthalmology and Visual Science · doi:10.1167/iovs.62.15.31 · Cited by 19
Ying, S., Yang, H., Gu, Q., Wu, Z., Zou, N., Wang, C., Wan, C., & Yuan, C. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109562 · Cited by 19
Notch3 destabilizes regulatory T cells to drive autoimmune neuroinflammation in multiple sclerosis
Benamar, M., Contini, P., Schmitz‐Abe, K., Lanzetta, O., Getachew, F., Bachelin, C., Leyva-Castillo, J. M., Wang, M., Öktelik, F. B., Perrot, O., et al. (2025) · Immunity · doi:10.1016/j.immuni.2025.09.007 · Cited by 17
Drohomyrecky, P. C., Doroshenko, E. R., Akkermann, R., Moshkova, M., Yi, T. J., Zhao, F. L., Ahn, J. J., McGaha, T. L., Pahan, K., & Dunn, S. E. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1801200 · Cited by 18
Jang, E., Cho, S., Pyo, S.-J., Nam, J., & Youn, J. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.631472 · Cited by 15
Modeling a complex disease: Multiple sclerosis—Update 2020
Regen, T., & Waisman, A. (2021) · Advances in immunology · doi:10.1016/bs.ai.2021.03.002 · Cited by 16
Self-citationSo, J.-B., Silver, P., Jittayasothorn, Y., Mattapallil, M., Chan, C.-C., Horai, R., & Caspi, R. (2020) · Journal of Autoimmunity · doi:10.1016/j.jaut.2020.102507 · Cited by 18
Santiago‐López, L., Hernández‐Mendoza, A., Vallejo‐Córdoba, B., Wall‐Medrano, A., & González-Córdova, A. F. (2021) · Trends in Food Science & Technology · doi:10.1016/j.tifs.2021.03.051 · Cited by 16
Fate-mapping mice: new tools and technology for immune discovery
Lee, S. E., Rudd, B. D., & Smith, N. L. (2022) · Trends in Immunology · doi:10.1016/j.it.2022.01.004 · Cited by 15
Metadata
- Authors
- Komuczki, J., Tuzlak, S., Friebel, E., Hartwig, T., Spath, S., Rosenstiel, P., Waisman, A., Opitz, L., Oukka, M., Schreiner, B., Pelczar, P., & Becher, B.
- Affiliations
- University of Zurich (CH)
- Christian-Albrechts-Universität zu Kiel (DE)
- University Medical Center of the Johannes Gutenberg University Mainz (DE)
- Seattle Children's Research Institute (US)
- Corresponding author
- Becher, Burkhard
- ORCID
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2019-05
- Volume
- 50
- Issue
- 5
- Pages
- 1289-1304.e6
- ISSN
- 1074-7613 (ISSN-L)
- OpenAlex
- W2944572075
- Cited by
- 201
- References
- 99
- Citations by year
- 2026: 18 · 2025: 27 · 2024: 22 · 2023: 24 · 2022: 27 · 2021: 36 · 2020: 34 · 2019: 12
- FWCI
- 10.89
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (acceptedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
- Zurich Open Repository and Archive (University of Zurich)
- Funders
- Swiss National Science Foundation (316030_150768, 310030_146130)
- European Community FP7 (602239)
- University Research Priority Program
- Austrian Academy of Science
- DFG Cluster of Excellence Inflammation at Interfaces
- EU H2020 (SYSCID (#733100))
- DFG (CRC/TR 128)
- Hertie Stiftung
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Keywords
- GM-CSF, T helper cells, neuroinflammation, multiple sclerosis, encephalitogenic T cells, IL-23, IL-1β, IL23R, IL-1 receptor, fate mapping, immunopathology, Th1 cells, Th17 cells
- MeSH terms
- Receptors, CXCR6, Animals, Female, Inflammation, Interferon-gamma, Male, Mice, Inbred C57BL, Tumor Necrosis Factor-alpha, Granulocyte-Macrophage Colony-Stimulating Factor, Receptors, Interleukin, Mice, Knockout, Th1 Cells, Mice, Receptors, Interleukin-1 Type I, Interleukin-1beta, Interleukin-23 Subunit p19, Th17 Cells
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review