Interleukin-23-Induced Transcription Factor Blimp-1 Promotes Pathogenicity of T Helper 17 Cells
Open accessAbstract
Interleukin-23 (IL-23) is a pro-inflammatory cytokine required for the pathogenicity of T helper 17 (Th17) cells but the molecular mechanisms governing this process remain unclear. We identified the transcription factor Blimp-1 (Prdm1) as a key IL-23-induced factor that drove the inflammatory function of Th17 cells. In contrast to thymic deletion of Blimp-1, which causes T cell development defects and spontaneous autoimmunity, peripheral deletion of this transcription factor resulted in reduced Th17 activation and reduced severity of autoimmune encephalomyelitis. Furthermore, genome-wide occupancy and overexpression studies in Th17 cells revealed that Blimp-1 co-localized with transcription factors RORγt, STAT-3, and p300 at the Il23r, Il17a/f, and Csf2 cytokine loci to enhance their expression. Blimp-1 also directly bound to and repressed cytokine loci Il2 and Bcl6. Taken together, our results demonstrate that Blimp-1 is an essential transcription factor downstream of IL-23 that acts in concert with RORγt to activate the Th17 inflammatory program.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
IL-23 and RORγt, essential mediators of Th17 differentiation, are required for colitis in multiple studies.
“However, multiple studies have shown that IL-23 and RORγt, which are essential mediators of Th17 differentiation, are required for colitis [127, 131, 132].”
From TH17 cell heterogeneity and its role in tissue inflammation (2023) · cites this paper as [131]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Bettelli, E., Carrier, Y., Gao, W., Korn, T., Strom, T. B., Oukka, M., Weiner, H. L., & Kuchroo, V. K. (2006) · Nature · doi:10.1038/nature04753 · Cited by 6,992 · see citing works
Ivanov, I. I., McKenzie, B. S., Zhou, L., Tadokoro, C. E., Lepelley, A., Lafaille, J. J., Cua, D. J., & Littman, D. R. (2006) · Cell · doi:10.1016/j.cell.2006.07.035 · Cited by 5,145 · see citing works
Self-citationIL-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 · see citing works
Self-citationVeldhoen, 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 · cited 2× · see citing works
“The early development of Th17 cells is initiated by transforming growth factor b (TGF-b) and IL-6 cytokine signaling (Bettelli et al., 2006; Mangan et al., 2006; Veldhoen et al., 2006), which induces expression of the lineage-specific transcription factor RORgt (Ivanov et al.”
Transforming growth factor-β induces development of the TH17 lineage
Mangan, P. R., Harrington, L. E., O'Quinn, D. B., Helms, W. S., Bullard, D. C., Elson, C. O., Hatton, R. D., Wahl, S. M., Schoeb, T. R., & Weaver, C. T. (2006) · Nature · doi:10.1038/nature04754 · Cited by 3,087 · see citing works
A Genome-Wide Association Study Identifies <i>IL23R</i> as an Inflammatory Bowel Disease Gene
Duerr, R. H., Taylor, K. D., Brant, S. R., Rioux, J. D., Silverberg, M. S., Daly, M. J., Steinhart, A. H., Abraham, C., Regueiro, M., Griffiths, A., et al. (2006) · Science · doi:10.1126/science.1135245 · Cited by 3,039 · see citing works
Development, cytokine profile and function of human interleukin 17-producing helper T cells
Wilson, N. J., Boniface, K., Chan, J. R., McKenzie, B. S., Blumenschein, W. M., Mattson, J. D., Basham, B., Smith, K., Chen, T., Morel, F., et al. (2007) · Nature Immunology · doi:10.1038/ni1497 · Cited by 2,035 · see citing works
Self-citationPhenotypic and functional features of human Th17 cells
Annunziato, F., Cosmi, L., Santarlasci, V., Maggi, L., Liotta, F., Mazzinghi, B., Parente, E., Filì, L., Ferri, S., Frosali, F., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070663 · Cited by 1,861 · see citing works
Johnston, R. J., Poholek, A. C., DiToro, D., Yusuf, I., Eto, D., Barnett, B., Dent, A. L., Craft, J., & Crotty, S. (2009) · Science · doi:10.1126/science.1175870 · Cited by 1,626 · see citing works
Targeted Disruption of the Mouse Stat1 Gene Results in Compromised Innate Immunity to Viral Disease
Durbin, J. E., Hackenmiller, R., Simon, M. C., & Levy, D. E. (1996) · Cell · doi:10.1016/s0092-8674(00)81289-1 · Cited by 1,522 · see citing works
McGeachy, M. J., Bak-Jensen, K. S., Chen, Y., Tato, C. M., Blumenschein, W., McClanahan, T., & Cua, D. J. (2007) · Nature Immunology · doi:10.1038/ni1539 · Cited by 1,520 · see citing works
Self-citationBcl6 mediates the development of T follicular helper cells
Nurieva, R. I., Chung, Y., Martinez, G. J., Yang, X. O., Tanaka, S., Matskevitch, T. D., Wang, Y.-H., & Dong, C. (2009) · Science · doi:10.1126/science.1176676 · Cited by 1,506 · see citing works
STAT3 Regulates Cytokine-mediated Generation of Inflammatory Helper T Cells
Yang, X. O., Panopoulos, A. D., Nurieva, R., Chang, S. H., Wang, D., Watowich, S. S., & Dong, C. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.c600321200 · Cited by 1,494 · see citing works
Generation of pathogenic TH17 cells in the absence of TGF-β signalling
Ghoreschi, K., Laurence, A., Yang, X.-P., Tato, C. M., McGeachy, M. J., Konkel, J. E., Ramos, H. L., Wei, L., Davidson, T. S., Bouladoux, N., et al. (2010) · Nature · doi:10.1038/nature09447 · Cited by 1,388 · see citing works
Self-citationParham, C. L., Chirica, M., Timans, J., Vaisberg, E., Travis, M. A., Cheung, J., Pflanz, S., Zhang, R. V., Singh, K. P., Vega, F., et al. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.168.11.5699 · Cited by 1,297 · see citing works
Self-citationCodarri, L., Gyülvészi, G., Tosevski, V., Hesske, L., Fontana, A., Magnenat, L., Suter, T., & Becher, B. (2011) · Nature Immunology · doi:10.1038/ni.2027 · Cited by 1,191 · cited 5× · see citing works
“Recent findings suggest that IL-23 operates through multiple pathways to generate mature pathogenic Th17 cells including maintenance of Th17 signature genes (Rorc and Il17), induction of effector genes (Il22, Csf2, and Ifng), suppression of repressive factors (Ahr, c-maf), and most importantly by enhancing its own sig…”
InfluentialFate mapping of IL-17-producing T cells in inflammatory responses
Hirota, K., Duarte, J. H., Veldhoen, M., Hornsby, E., Li, Y., Cua, D. J., Ahlfors, H., Wilhelm, C., Tolaini, M., Menzel, U., et al. (2011) · Nature Immunology · doi:10.1038/ni.1993 · Cited by 1,176 · see citing works
Self-citationInduction and molecular signature of pathogenic TH17 cells
Lee, Y., Awasthi, A., Yosef, N., Quintana, F. J., Xiao, S., Peters, A., Wu, C., Kleinewietfeld, M., Kunder, S., Hafler, D. A., et al. (2012) · Nature Immunology · doi:10.1038/ni.2416 · Cited by 1,174 · see citing works
A Validated Regulatory Network for Th17 Cell Specification
Ciofani, M., Madar, A., Galan, C., Sellars, M., Mace, K., Pauli, F., Agarwal, A., Huang, W., Parkurst, C. N., Muratet, M., et al. (2012) · Cell · doi:10.1016/j.cell.2012.09.016 · Cited by 1,160 · see citing works
McGeachy, M. J., Chen, Y., Tato, C. M., Laurence, A., Joyce-Shaikh, B., Blumenschein, W. M., McClanahan, T. K., O'Shea, J. J., & Cua, D. J. (2009) · Nature Immunology · doi:10.1038/ni.1698 · Cited by 1,074 · see citing works
Self-citationEl-Behi, M., Ciric, B., Dai, H., Yan, Y., Cullimore, M., Safavi, F., Zhang, G.-X., Dittel, B. N., & Rostami, A. (2011) · Nature Immunology · doi:10.1038/ni.2031 · Cited by 1,071 · cited 2× · see citing works
“…of effector genes (Il22, Csf2, and Ifng), suppression of repressive factors (Ahr, c-maf), and most importantly by enhancing its own signal strength through upregulation of Il23r expression (Codarri et al., 2011; El-Behi et al., 2011; Ghoreschi et al., 2010; Hirota et al., 2011; Lee et al., 2012).”
Shelef, M. A., Lin, K., McHeyzer‐Williams, L. J., Liao, J., McHeyzer‐Williams, M. G., & Calame, K. L. (2003) · Immunity · doi:10.1016/s1074-7613(03)00267-x · Cited by 839 · see citing works
Chan, J. R., Blumenschein, W. M., Murphy, E., Diveu, C., Wiekowski, M., Abbondanzo, S. J., Lucian, L. A., Geissler, R. H., Brodie, S. J., Kimball, A. B., et al. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20060244 · Cited by 679 · see citing works
Self-citationRutishauser, R. L., Martins, G. A., Kalachikov, S. M., Chandele, A., Parish, I. A., Meffre, E., Jacob, J., Calame, K. L., & Kaech, S. M. (2009) · Immunity · doi:10.1016/j.immuni.2009.05.014 · Cited by 612 · see citing works
Cretney, E., Xin, A., Shi, W., Minnich, M., Masson, F., Miasari, M., Belz, G. T., Smyth, G. K., Busslinger, M., Nutt, S. L., et al. (2011) · Nature Immunology · doi:10.1038/ni.2006 · Cited by 605 · see citing works
Preferential recruitment of interferon‐γ–expressing T <sub>H</sub> 17 cells in multiple sclerosis
Kebir, H., Ifergan, I., Alvarez, J. I., Bernard, M., Poirier, J., Arbour, N., Duquette, P., & Prat, A. (2009) · Annals of Neurology · doi:10.1002/ana.21748 · Cited by 551 · see citing works
Kallies, A., Xin, A., Belz, G. T., & Nutt, S. L. (2009) · Immunity · doi:10.1016/j.immuni.2009.06.021 · Cited by 505 · see citing works
Shin, H., Blackburn, S. D., Intlekofer, A. M., Kao, C., Angelosanto, J., Reiner, S. L., & Wherry, E. J. (2009) · Immunity · doi:10.1016/j.immuni.2009.06.019 · Cited by 481 · see citing works
Transcriptional repressor Blimp-1 regulates T cell homeostasis and function
Martins, G. A., Cimmino, L., Shelef, M. A., Szabolcs, M. J., Herron, A. J., Magnúsdóttir, E., & Calame, K. L. (2006) · Nature Immunology · doi:10.1038/ni1320 · Cited by 372 · see citing works
Chabaud, M., Lubberts, E., Joosten, L., van den Berg, W., & Miossec, P. (2001) · Arthritis Research & Therapy · doi:10.1186/ar294 · Cited by 333 · see citing works
Lee, C.-K., Raz, R., Gimeno, R., Gertner, R., Wistinghausen, B., Takeshita, K., DePinho, R. A., & Levy, D. E. (2002) · Immunity · doi:10.1016/s1074-7613(02)00336-9 · Cited by 242 · see citing works
TGF-β signaling to T cells inhibits autoimmunity during lymphopenia-driven proliferation
Zhang, N., & Bevan, M. J. (2012) · Nature Immunology · doi:10.1038/ni.2319 · Cited by 175 · see citing works
Zhang, D. J., Wang, Q., Wei, J., Baimukanova, G., Buchholz, F., Stewart, A. F., Mao, X., & Killeen, N. P. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.11.6725 · Cited by 132 · see citing works
Salehi, S., Bankoti, R., Benevides, L., Willen, J., Couse, M., Silva, J. S., Dhall, D., Meffre, E., Targan, S. R., & Martins, G. A. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201966 · Cited by 50 · see citing works
Lin, M.-H., Chou, F., Yeh, L.-T., Fu, S., Chiou, H., Lin, K., Chang, D., & Sytwu, H. (2012) · Diabetologia · doi:10.1007/s00125-012-2722-y · Cited by 40 · see citing works
Lin, M.-H., Yeh, L., Chen, S., Chiou, H.-Y. C., Chu, C., Yen, L. B., Lin, K., Chang, D., & Sytwu, H. (2014) · Clinical Immunology · doi:10.1016/j.clim.2014.02.006 · Cited by 35 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- Kebir H, Ifergan I, Alvarez JI, Bernard M, Poirier J, Arbour N, Duquette P, and Prat A. (2009). Preferential recruitment of interferon-gamma-expressing TH17 cells in multiple sclerosis. Ann Neurol 66, 390– 402. 19810097
Cited by
Sorted by citations
The microbiota in adaptive immune homeostasis and disease
Honda, K., & Littman, D. R. (2016) · Nature · doi:10.1038/nature18848 · Cited by 1,846 · see citing works
The pathogenicity of Th17 cells in autoimmune diseases
Yasuda, K., Takeuchi, Y., & Hirota, K. (2019) · Seminars in Immunopathology · doi:10.1007/s00281-019-00733-8 · Cited by 560 · see citing works
The spectrum of T cell metabolism in health and disease
Bantug, G. R., Galluzzi, L., Kroemer, G., & Hess, C. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2017.99 · Cited by 421 · see citing works
The dichotomous nature of T helper 17 cells
Stockinger, B., & Omenetti, S. (2017) · Nature reviews. Immunology · doi:10.1038/nri.2017.50 · Cited by 399 · see citing works
Pathogenesis of ankylosing spondylitis — recent advances and future directions
Ranganathan, V., Gracey, E., Brown, M. A., Inman, R. D., & Haroon, N. (2017) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2017.56 · Cited by 313 · see citing works
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 · see citing works
T cell responses in the central nervous system
Korn, T., & Kallies, A. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2016.144 · Cited by 268 · see citing works
Gut microorganisms act together to exacerbate inflammation in spinal cords
Miyauchi, E., Kim, S.-W., Suda, W., Kawasumi, M., Onawa, S., Taguchi-Atarashi, N., Morita, H., Taylor, T. D., Hattori, M., & Ohno, H. (2020) · Nature · doi:10.1038/s41586-020-2634-9 · Cited by 268 · see citing works
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 · see citing works
Roles of GM-CSF in the Pathogenesis of Autoimmune Diseases: An Update
Lotfi, N., Thomé, R., Rezaei, N., Zhang, G., Rezaei, A., Rostami, A. M., & Esmaeil, N. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01265 · Cited by 229 · see citing works
The role of inflammation in autoimmune disease: a therapeutic target
Xiang, Y., Zhang, M., Jiang, D., Su, Q., & Shi, J. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1267091 · Cited by 217 · see citing works
Henriksson, J., Chen, X. X., Gomes, T., Ullah, U., Meyer, K. B., Miragaia, R. J., Duddy, G., Pramanik, J., Yusa, K., Lahesmaa, R., et al. (2019) · Cell · doi:10.1016/j.cell.2018.11.044 · Cited by 195 · see citing works
van Hamburg, J. P., & Tas, S. W. (2017) · Journal of Autoimmunity · doi:10.1016/j.jaut.2017.12.006 · Cited by 186 · see citing works
Th17 cell pathogenicity and plasticity in rheumatoid arthritis
Yang, P., Qian, F., Zhang, M.-F., Xu, A., Wang, X., Jiang, B., & Zhou, L. (2019) · Journal of Leukocyte Biology · doi:10.1002/jlb.4ru0619-197r · Cited by 187 · see citing works
Shin, B., Benavides, G. A., Geng, J., Koralov, S. B., Hu, H., Darley-Usmar, V. M., & Harrington, L. E. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.022 · Cited by 178 · see citing works
Recent advances in understanding the Th1/Th2 effector choice
Butcher, M. J., & Zhu, J. (2021) · Faculty Reviews · doi:10.12703/r/10-30 · Cited by 180 · see citing works
JunB promotes Th17 cell identity and restrains alternative CD4+ T-cell programs during inflammation
Carr, T. M., Wheaton, J. D., Houtz, G. M., & Ciofani, M. (2017) · Nature Communications · doi:10.1038/s41467-017-00380-3 · Cited by 141 · see citing works
Choi, J., Diao, H., Faliti, C. E., Truong, J., Rossi, M., Bélanger, S., Yu, B., Goldrath, A. W., Pipkin, M. E., & Crotty, S. (2020) · Nature Immunology · doi:10.1038/s41590-020-0706-5 · Cited by 143 · see citing works
IL-23 past, present, and future: a roadmap to advancing IL-23 science and therapy
Krueger, J. G., Eyerich, K., Kuchroo, V. K., Ritchlin, C. T., Abreu, M. T., Elloso, M. M., Fourie, A. M., Fakharzadeh, S. S., Sherlock, J. P., Yang, Y., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1331217 · Cited by 156 · see citing works
Self-citationLessons Learned From Trials Targeting Cytokine Pathways in Patients With Inflammatory Bowel Diseases
Abraham, C., Dulai, P. S., Vermeire, S., & Sandborn, W. J. (2016) · Gastroenterology · doi:10.1053/j.gastro.2016.10.018 · Cited by 141 · see citing works
Recent advances in ankylosing spondylitis: understanding the disease and management
Garcia‐Montoya, L., Gul, H. L., & Emery, P. (2018) · F1000Research · doi:10.12688/f1000research.14956.1 · Cited by 144 · see citing works
Al‐Mossawi, H., Chen, L., Fang, H., Ridley, A., de Wit, J., Yager, N., Hammitzsch, A., Pulyakhina, I., Fairfax, B. P., Simone, D., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-01771-2 · Cited by 138 · see citing works
The genetic background of inflammatory bowel disease: from correlation to causality
Venema, W. T. U., Voskuil, M. D., Dijkstra, G. D. H., Weersma, R. K., & Festen, E. A. M. (2016) · The Journal of Pathology · doi:10.1002/path.4817 · Cited by 126 · see citing works
IL-17-producing γδ T cells switch migratory patterns between resting and activated states
McKenzie, D. R., Kara, E. E., Bastow, C. R., Tyllis, T. S., Fenix, K. A., Whyte, C. E., Wilson, J. J., Babb, R., Paton, J. C., Kallies, A., et al. (2017) · Nature Communications · doi:10.1038/ncomms15632 · Cited by 118 · see citing works
Fu, S., Yeh, L., Chu, C., Yen, B., & Sytwu, H. (2017) · Journal of Biomedical Science · doi:10.1186/s12929-017-0354-8 · Cited by 119 · see citing works
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 118 · see citing works
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 106 · see citing works
Why did IL-23p19 inhibition fail in AS: a tale of tissues, trials or translation?
Siebert, S., Millar, N. L., & McInnes, I. B. (2018) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2018-213654 · Cited by 100 · see citing works
The obesity-related pathology and Th17 cells
Endo, Y., Yokote, K., & Nakayama, T. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2399-3 · Cited by 98 · see citing works
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 95 · see citing works
Franken, A., Mol, P. V., Vanmassenhove, S., Donders, E., Schepers, R., Brussel, T. V., Dooms, C., Yserbyt, J., Crem, N. D., Testelmans, D., et al. (2022) · Journal for ImmunoTherapy of Cancer · doi:10.1136/jitc-2022-005323 · Cited by 89 · see citing works
JunB is essential for IL-23-dependent pathogenicity of Th17 cells
Hasan, Z., Koizumi, S.-I., Sasaki, D., Yamada, H., Arakaki, N., Fujihara, Y., Okitsu, S., Shirahata, H., & Ishikawa, H. (2017) · Nature Communications · doi:10.1038/ncomms15628 · Cited by 95 · see citing works
Chen, X., Sunkel, B. D., Wang, M., Kang, S., Wang, T., Gnanaprakasam, J. R., Liu, L., Cassel, T., Scott, D. A., Muñoz-Cabello, A. M., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abm8161 · Cited by 93 · see citing works
Cho, J. J., Xu, Z., Parthasarathy, U., Drashansky, T. T., Helm, E. Y., Zuniga, A. N., Lorentsen, K. J., Mansouri, S., Cho, J. Y., Edelmann, M. J., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08605-3 · Cited by 91 · see citing works
Update on regulation and effector functions of Th17 cells
Sandquist, I., & Kolls, J. K. (2018) · F1000Research · doi:10.12688/f1000research.13020.1 · Cited by 91 · see citing works
Pawlak, M., Ho, A. W., & Kuchroo, V. K. (2020) · Current Opinion in Immunology · doi:10.1016/j.coi.2020.09.001 · Cited by 89 · see citing works
Regulation of Orbital Fibrosis and Adipogenesis by Pathogenic Th17 Cells in Graves Orbitopathy
Fang, S., Huang, Y., Zhong, S., Li, Y., Zhang, Y., Li, Y., Sun, J. P., Liu, X., Wang, Y., Zhang, S., et al. (2017) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2017-01349 · Cited by 86 · see citing works
The Lysine Methyltransferase G9a in Immune Cell Differentiation and Function
Scheer, S., & Zaph, C. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00429 · Cited by 84 · see citing works
TH17 cell plasticity: The role of dendritic cells and molecular mechanisms
Agalioti, T., Villablanca, E. J., Huber, S., & Gagliani, N. (2018) · Journal of Autoimmunity · doi:10.1016/j.jaut.2017.12.003 · Cited by 73 · see citing works
Ogawa, C., Bankoti, R., Nguyen, T., Hassanzadeh‐Kiabi, N., Nadeau, S., Porritt, R. A., Couse, M., Fan, X., Dhall, D., Eberl, G., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.09.016 · Cited by 72 · see citing works
Bishu, S., Zaatari, M. E., Hayashi, A., Hou, G., Bowers, N., Kinnucan, J. A. R., Manoogian, B., Muza–Moons, M. M., Zhang, M., Grasberger, H., et al. (2019) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjz010 · Cited by 71 · see citing works
Th17 cell pathogenicity in autoimmune disease
Park, E., & Ciofani, M. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01535-9 · Cited by 75 · see citing works
The IL-12 Cytokine and Receptor Family in Graft-vs.-Host Disease
Bastian, D. A., Wu, Y., Betts, B. C., & Yu, X. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00988 · Cited by 73 · see citing works
Rutz, S., Eidenschenk, C., Kiefer, J. R., & Ouyang, W. (2016) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2016.07.004 · Cited by 69 · see citing works
Tang, L., Yang, X. T., Liang, Y., Xie, H., Dai, Z., & Zheng, G. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01210 · Cited by 68 · see citing works
Lipid metabolism in Th17 cell function
Kanno, T., Nakajima, T., Miyako, K., & Endo, Y. (2023) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2023.108411 · Cited by 67 · see citing works
IL-23 stabilizes an effector Treg cell program in the tumor microenvironment
Wertheimer, T., Zwicky, P., Rindlisbacher, L., Sparano, C., Vermeer, M., de Melo, B. M. S., Haftmann, C., Rückert, T., Sethi, A., Schärli, S., et al. (2024) · Nature Immunology · doi:10.1038/s41590-024-01755-7 · Cited by 68 · see citing works
The Functional Stability of FOXP3 and RORγt in Treg and Th17 and Their Therapeutic Applications
Ren, J., & Li, B. (2016) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2016.10.002 · Cited by 63 · see citing works
IL-23 and Th17 Disease in Inflammatory Arthritis
Yago, T., Nanke, Y., Kawamoto, M., Kobashigawa, T., Yamanaka, H., & Kotake, S. (2017) · Journal of Clinical Medicine · doi:10.3390/jcm6090081 · Cited by 64 · see citing works
Differential regulation of Effector and Regulatory T cell function by Blimp1
Bankoti, R., Ogawa, C., Nguyen, T., Emadi, L., Couse, M., Salehi, S., Fan, X., Dhall, D., Wang, Y., Brown, J. S., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-12171-3 · Cited by 61 · see citing works
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 · see citing works
Ciaffi, J., Mitselman, D., Mancarella, L., Brusi, V., Lisi, L., Ruscitti, P., Cipriani, P., Melicòni, R., Giacomelli, R., Borghi, C., et al. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.792846 · Cited by 58 · see citing works
He, Z.-H., Ma, J., Wang, R., Zhang, J., Huang, Z.-F., Wang, F., Sen, S., Rothenberg, E., & Sun, Z.-M. (2017) · Nature Immunology · doi:10.1038/ni.3832 · Cited by 49 · see citing works
Satb1 regulates the effector program of encephalitogenic tissue Th17 cells in chronic inflammation
Yasuda, K., Kitagawa, Y., Kawakami, R., Isaka, Y., Watanabe, H., Kondoh, G., Kohwi-shigematsu, T., Sakaguchi, S., & Hirota, K. (2019) · Nature Communications · doi:10.1038/s41467-019-08404-w · Cited by 52 · see citing works
Noncanonical STAT3 activity sustains pathogenic Th17 proliferation and cytokine response to antigen
Poholek, C. H., Raphael, I., Wu, D.-W., Revu, S., Rittenhouse, N. L., Uche, U. U., Majumder, S., Kane, L., Poholek, A., & McGeachy, M. (2020) · Journal of Experimental Medicine · doi:10.1084/jem.20191761 · Cited by 50 · see citing works
Self-citationCytokines that Modulate the Differentiation of Th17 Cells in Autoimmune Uveitis
Guo, K., & Zhang, X. (2021) · Journal of Immunology Research · doi:10.1155/2021/6693542 · Cited by 54 · see citing works
The Yin and Yang of IL-17 in Systemic Sclerosis
Wei, L., Abraham, D., & Ong, V. H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.885609 · Cited by 54 · see citing works
Feo, D. D., Merlini, A., Brambilla, E., Ottoboni, L., Laterza, C., Menon, R., Srinivasan, S., Farina, C., Manteiga, J. M. G., Butti, E., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci92387 · Cited by 54 · see citing works
Komorowski, A. S., & Pezo, R. C. (2019) · Breast Cancer Research and Treatment · doi:10.1007/s10549-019-05472-w · Cited by 54 · see citing works
Blimp-1 is essential for allergen-induced asthma and Th2 cell development in the lung
He, K., Hettinga, A., Kale, S. L., Hu, S., Xie, M. M., Dent, A. L., Ray, A., & Poholek, A. C. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20190742 · Cited by 52 · see citing works
Chuang, H., Tsai, C., Hsueh, C., & Tan, T. (2018) · Science Advances · doi:10.1126/sciadv.aat5401 · Cited by 52 · see citing works
Fang, S., Huang, Y., Zhong, S., Zhang, Y., Liu, X., Wang, Y., Gu, P., Zhou, H., & Fan, X. (2016) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.16-20199 · Cited by 48 · see citing works
CCAAT/Enhancer-binding protein β promotes pathogenesis of EAE
Simpson-Abelson, M. R., Hernández-Mir, G., Childs, E. E., Cruz, J. A., Poholek, A. C., Chattopadhyay, A., Gaffen, S. L., & McGeachy, M. J. (2017) · Cytokine · doi:10.1016/j.cyto.2017.01.005 · Cited by 45 · see citing works
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 45 · see citing works
Na, S.-Y., Janakiraman, M., Leliavski, A., & Krishnamoorthy, G. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2025944118 · Cited by 45 · see citing works
Shetty, A., Tripathi, S. K., Junttila, S., Buchacher, T., Biradar, R., Bhosale, S. D., Envall, T., Laiho, A., Moulder, R., Rasool, O., et al. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac256 · Cited by 44 · see citing works
Uchiyama, R., Yonehara, S., Taniguchi, S., Ishido, S., Ishii, K. J., & Tsutsui, H. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601373 · Cited by 42 · see citing works
Tolerance to the Intestinal Microbiota Mediated by ROR(γt) + Cells
Ohnmacht, C. (2016) · Trends in Immunology · doi:10.1016/j.it.2016.05.002 · Cited by 42 · see citing works
Nanjappa, S. G., McDermott, A. J., Fites, J. S., Galles, K., Wüthrich, M., Deepe, G. S., & Klein, B. S. (2017) · PLoS Pathogens · doi:10.1371/journal.ppat.1006356 · Cited by 40 · see citing works
CD4+ T-cell subsets in autoimmune hepatitis: A review
Chen, H., Han, Z., Fan, Y., Chen, L., Peng, F., Cheng, X., Wang, Y., Su, J., & Li, D. (2023) · Hepatology Communications · doi:10.1097/hc9.0000000000000269 · Cited by 40 · see citing works
Biofilm‐induced profiles of immune response gene expression by oral epithelial cells
Ebersole, J. L., Peyyala, R., & Gonzalez, O. A. (2019) · Molecular Oral Microbiology · doi:10.1111/omi.12251 · Cited by 39 · see citing works
Functional and phenotypic heterogeneity of Th17 cells in health and disease
Byström, J., Clanchy, F. I. L., Taher, T. E. I., Al-Bogami, M. M., Ong, V. H., Abraham, D., Williams, R. O., & Mageed, R. A. (2018) · European Journal of Clinical Investigation · doi:10.1111/eci.13032 · Cited by 37 · see citing works
Immunometabolism of Tregs: mechanisms, adaptability, and therapeutic implications in diseases
Lu, Y., Wang, Y., Ruan, T., Wang, Y., Ju, L., Zhou, M., Liu, L., Dengfu, Y., & Yao, M. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1536020 · Cited by 39 · see citing works
Crossing the boundaries: IL-23 and its role in linking inflammation of the skin, gut and joints
Łukasik, Z. M., Gracey, E., Venken, K., Ritchlin, C. T., & Elewaut, D. S. (2021) · Lara D. Veeken · doi:10.1093/rheumatology/keab385 · Cited by 36 · see citing works
Making sense of IL‐6 signalling cues in pathophysiology
Millrine, D., Jenkins, R. L., Hughes, S. T. O., & Jones, S. A. (2021) · FEBS Letters · doi:10.1002/1873-3468.14201 · Cited by 38 · see citing works
Functional heterogeneity of human skin‐resident memory T cells in health and disease
Strobl, J., & Haniffa, M. A. (2023) · Immunological Reviews · doi:10.1111/imr.13213 · Cited by 33 · see citing works
Mangani, D., Subramanian, A., Huang, L., Cheng, H., Krovi, S. H., Wu, Y., Yang, D., Moreira, T. G., Escobar, G., Schnell, A., et al. (2024) · Immunity · doi:10.1016/j.immuni.2024.09.017 · Cited by 35 · see citing works
Poholek, A. C., Jankovic, D. L., Villarino, A. V., Petermann, F., Hettinga, A., Shouval, D. S., Snapper, S. B., Kaech, S. M., Brooks, S. R., Vahedi, G., et al. (2016) · Science Immunology · doi:10.1126/sciimmunol.aaf8612 · Cited by 34 · see citing works
Self-citationZhao, Y., Liu, Z., Qin, L., Wang, T., & Bai, O. (2021) · Molecular Immunology · doi:10.1016/j.molimm.2021.03.010 · Cited by 30 · see citing works
Interleukin‐33 alleviates psoriatic inflammation by suppressing the T helper type 17 immune response
Chen, Z., Hu, Y., Gong, Y., Zhang, X., Cui, L., Chen, R., Yu, Y., Yu, Q., Chen, Y., Diao, H., et al. (2020) · Immunology · doi:10.1111/imm.13203 · Cited by 30 · see citing works
Self-citationIL-2 Shapes the Survival and Plasticity of IL-17–Producing γδ T Cells
Corpuz, T. M., Vazquez-Lombardi, R., Luong, J. K., Warren, J. A., Stolp, J., Christ, D., King, C., Brink, R. A., Sprent, J., & Webster, K. E. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700335 · Cited by 30 · see citing works
Choi, G., Park, Y., Cho, M., Moon, H., Kim, D., Kang, C., Chung, Y., & Kim, B. (2021) · Experimental & Molecular Medicine · doi:10.1038/s12276-021-00632-9 · Cited by 28 · see citing works
Metabolic regulation and function of T helper cells in neuroinflammation
Spiljar, M., & Kuchroo, V. K. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00959-z · Cited by 29 · see citing works
Lu, Y., Ma, Q., Yu, L., Huang, H., Liu, X., Chen, P., Ran, H., & Liu, W. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109693 · Cited by 28 · see citing works
Interleukin 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 31 · see citing works
Bao, S., Zheng, J., Li, N., Huang, C., Chen, M., Cheng, Q., Li, Q., Lü, Q., Zhu, M., Ling, Q., et al. (2016) · Clinics and Research in Hepatology and Gastroenterology · doi:10.1016/j.clinre.2016.10.005 · Cited by 27 · see citing works
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 · see citing works
Pu, D., Zhang, Z., & Feng, B. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.906419 · Cited by 25 · see citing works
Dynamics of helper CD4 T cells during acute and stable allergic asthma
Lu, Y., Kared, H., Tan, S. W., Becht, É., Newell, E. W., Bever, H. P. S. V., Ng, T. P., & Larbi, A. (2018) · Mucosal Immunology · doi:10.1038/s41385-018-0057-9 · Cited by 24 · see citing works
Cellular metabolism dictates T cell effector function in health and disease
Kolan, S. S., Li, G., Wik, J. A., Malachin, G., Guo, S., Kolan, P., & Skålhegg, B. S. (2020) · Scandinavian Journal of Immunology · doi:10.1111/sji.12956 · Cited by 24 · see citing works
An autoimmune transcriptional circuit drives FOXP3 + regulatory T cell dysfunction
Sumida, T. S., Lincoln, M. R., He, L., Park, Y., Ota, M., Oguchi, A., Son, R., Yi, A., Stillwell, H. A., Leissa, G. A., et al. (2024) · Science Translational Medicine · doi:10.1126/scitranslmed.adp1720 · Cited by 25 · see citing works
Emerging Complexity in CD4+T Lineage Programming and Its Implications in Colorectal Cancer
Ditoro, D. F., & Basu, R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.694833 · Cited by 23 · see citing works
Janoschka, C., Lindner, M., Koppers, N., Starost, L. J., Liebmann, M., Eschborn, M., Schneider‐Hohendorf, T., Windener, F., Schafflick, D., Fleck, A.-K., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2209944120 · Cited by 22 · see citing works
Th17 cells in the liver: balancing autoimmunity and pathogen defense
Taniki, N., Nakamoto, N., Chu, P., Ichikawa, M., Teratani, T., & Kanai∥, T. (2022) · Seminars in Immunopathology · doi:10.1007/s00281-022-00917-9 · Cited by 21 · see citing works
Fatty Acid Metabolism and T Cells in Multiple Sclerosis
Pompura, S. L., Hafler, D. A., & Dominguez‐Villar, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.869197 · Cited by 21 · see citing works
Granulocyte-macrophage colony-stimulating factor as a mediator of autoimmunity in multiple sclerosis
Kostić, M. S., Živković, N., Cvetanović, A., & Stojanović, I. R. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.07.002 · Cited by 20 · see citing works
Wang, W., Li, Y., Liu, Z., Liu, L.-X., Lin, J., Liu, Z.-Y., Chen, X.-P., Zhang, W., Xu, Z., Shi, T., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00476-w · Cited by 19 · see citing works
Inhibition of autoimmune Th17 cell responses by pain killer ketamine
Lee, J.-E., Lee, J., Park, Y.-J., Kim, B. S., Jeon, Y.-T., & Chung, Y. (2017) · Oncotarget · doi:10.18632/oncotarget.18324 · Cited by 19 · see citing works
Acerbi, E., Viganò, E., Poidinger, M., Mortellaro, A., Zelante, T., & Stella, F. A. (2016) · Scientific Reports · doi:10.1038/srep23128 · Cited by 18 · see citing works
Layman, A., Sprout, S., Phillips, D., & Oliver, P. (2017) · Scientific Reports · doi:10.1038/srep39649 · Cited by 19 · see citing works
- Authors
- Jain, R., Chen, Y., Kanno, Y., Joyce-Shaikh, B., Vahedi, G., Hirahara, K., Blumenschein, W. M., Sukumar, S., Haines, C. J., Sadekova, S., McClanahan, T. K., McGeachy, M. J., O’Shea, J. J., & Cua, D. J.
- Affiliations
- Merck & Co., Inc., Rahway, NJ, USA (United States) (US)
- National Institutes of Health (US)
- Corresponding author
- Cua, Daniel J.
- ORCID
- Venue
- Immunity
- Publisher
- Elsevier BV
- Published
- 2016-01
- Volume
- 44
- Issue
- 1
- Pages
- 131-142
- ISSN
- 1074-7613 (ISSN-L)
- PMC
- PMC11608061
- OpenAlex
- W2196731768
- Cited by
- 167
- References
- 36
- Citations by year
- 2026: 10 · 2025: 9 · 2024: 14 · 2023: 16 · 2022: 19 · 2021: 20 · 2020: 18 · 2019: 11 · 2018: 12 · 2017: 24 · 2016: 13
- FWCI
- 8.05
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Immunity (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (ZIAAR041159)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
- Keywords
- IL-23, Blimp-1, Th17 cells, RORγt, STAT3, P300, transcriptional repression, autoimmune encephalomyelitis, cytokine gene expression, BCL6, Th17 cell differentiation
- MeSH terms
- Positive Regulatory Domain I-Binding Factor 1, Animals, Cell Differentiation, Cell Separation, Encephalomyelitis, Autoimmune, Experimental, Gene Expression Regulation, Inflammation, Lymphocyte Activation, Mice, Inbred C57BL, Mice, Transgenic, Transcription Factors, Transduction, Genetic, Mice, Knockout, Chromatin Immunoprecipitation, Mice, Interleukin-23, Th17 Cells, Real-Time Polymerase Chain Reaction
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