The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
The aryl hydrocarbon receptor links TH17-cell-mediated autoimmunity to environmental toxins
Open accessAbstract
The aryl hydrocarbon receptor (AHR) is a ligand-dependent transcription factor best known for mediating the toxicity of dioxin. Environmental factors are believed to contribute to the increased prevalence of autoimmune diseases, many of which are due to the activity of T(H)17 T cells, a new helper T-cell subset characterized by the production of the cytokine IL-17. Here we show that in the CD4+ T-cell lineage of mice AHR expression is restricted to the T(H)17 cell subset and its ligation results in the production of the T(H)17 cytokine interleukin (IL)-22. AHR is also expressed in human T(H)17 cells. Activation of AHR by a high-affinity ligand during T(H)17 cell development markedly increases the proportion of T(H)17 T cells and their production of cytokines. CD4+ T cells from AHR-deficient mice can develop T(H)17 cell responses, but when confronted with AHR ligand fail to produce IL-22 and do not show enhanced T(H)17 cell development. AHR activation during induction of experimental autoimmune encephalomyelitis causes accelerated onset and increased pathology in wild-type mice, but not AHR-deficient mice. AHR ligands may therefore represent co-factors in the development of autoimmune diseases.
Overview
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
Verification
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“it was demonstrated that expression of IL-22 requires the AhR (Martin et al., 2009; Veldhoen et al., 2008).”
From Understanding the Holobiont: How Microbial Metabolites Affect Human Health and Shape the Immune System (2017) · cites this paper as Veldhoen et al., 2008
Experimental — accuracy not yet measuredIn the citing paper
“Accordingly, many phenotypes of Ahr mutant models such as altered hepatovascular development and impaired immune function, do not appear to be directly related to TCDD toxicity or adaptive metabolism (Quintana et al., 2008; Stockinger et al., 2014; Veldhoen et al., 2008; Walisser et al., 2005)”
From Rodent Genetic Models of Ah Receptor Signaling (2021) · cites this paper as Veldhoen et al., 2008
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
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
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
Liang, S. C., Tan, X.-Y., Luxenberg, D. P., Karim, R., Dunussi-Joannopoulos, K., Collins, M., & Fouser, L. A. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20061308 · Cited by 2,330
Interleukin-22, a TH17 cytokine, mediates IL-23-induced dermal inflammation and acanthosis
Zheng, Y., Danilenko, D. M., Valdez, P. A., Kasman, I. M., Eastham‐Anderson, J., Wu, J., & Ouyang, W. (2006) · Nature · doi:10.1038/nature05505 · Cited by 1,888
Surface phenotype and antigenic specificity of human interleukin 17–producing T helper memory cells
Acosta-Rodriguez, E. V., Rivino, L., Geginat, J., Jarrossay, D., Gattorno, M., Lanzavecchia, A., Sallusto, F., & Napolitani, G. (2007) · Nature Immunology · doi:10.1038/ni1467 · Cited by 1,828
Kebir, H., Kreymborg, K., Ifergan, I., Dodelet-Devillers, A., Cayrol, R., Bernard, M., Giuliani, F., Arbour, N., Becher, B., & Prat, A. (2007) · Nature Medicine · doi:10.1038/nm1651 · Cited by 1,759
Immune System Impairment and Hepatic Fibrosis in Mice Lacking the Dioxin-Binding Ah Receptor
Fernandez-Salguero, P., Pineau, T., Hilbert, D. M., McPhail, T., Lee, S. S. T., Kimura, S., Nebert, D. W., Rudikoff, S., Ward, J. M., & Gonzalez, F. J. (1995) · Science · doi:10.1126/science.7732381 · Cited by 1,075
Hirota, K., Yoshitomi, H., Hashimoto, M., Maeda, S., Teradaira, S., Sugimoto, N., Yamaguchi, T., Nomura, T., Ito, H., Nakamura, T., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20071397 · Cited by 937
Self-citationSchmidt, J. V., Su, G. H., Reddy, J. K., Simon, M. C., & Bradfield, C. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6731 · Cited by 902
AH RECEPTOR SIGNALING PATHWAYS
Schmidt, J. V., & Bradfield, C. A. (1996) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.12.1.55 · Cited by 899
Cited by
Sorted by citations
Items 501–600 of 1,001
Rannug, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21165681 · Cited by 83
Effect of polycyclic aromatic hydrocarbons on immunity
Yu, Y., Jin, H., & Lu, Q. (2022) · Journal of Translational Autoimmunity · doi:10.1016/j.jtauto.2022.100177 · Cited by 84
Basso, A. S., Cheroutre, H., & Mucida, D. (2009) · Cell Research · doi:10.1038/cr.2009.26 · Cited by 81
Association between Smoking and Uveitis
Yuen, B. G., Tham, V. M., Browne, E. N., Weinrib, R., Borkar, D. S., Parker, J. V., Uchida, A., Vinoya, A. C., & Acharya, N. R. (2015) · Ophthalmology · doi:10.1016/j.ophtha.2015.02.034 · Cited by 81
An, J., Golech, S., Klaewsongkram, J., Zhang, Y., Subedi, K., Huston, G. E., Wood, W. H., Wersto, R. P., Becker, K. G., Swain, S. L., et al. (2011) · The FASEB Journal · doi:10.1096/fj.11-186924 · Cited by 81
Barilla, R., Diskin, B. E., Caso, R. C., Lee, K. B., Mohan, N., Buttar, C., Adam, S., Sekendiz, Z., Wang, J., Salas, R. D., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09416-2 · Cited by 81
Wang, E., Liu, X., Tu, W., Do, D. C., Yu, H., Yang, L., Zhou, Y., Xu, D., Huang, S., Yang, P., et al. (2019) · Allergy · doi:10.1111/all.13784 · Cited by 83
Th17 plasticity and its changes associated with inflammatory bowel disease
Ueno, A. (2015) · World Journal of Gastroenterology · doi:10.3748/wjg.v21.i43.12283 · Cited by 82
Ye, M., Zhang, Y., Gao, H., Xu, Y., Jing, P., Wu, J., Zhang, X., Xiong, J., Dong, C., Yao, L., et al. (2017) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-17-0396 · Cited by 85
Manasson, J., Wallach, D. S., Guggino, G., Stapylton, M., Badri, M. H., Solomon, G. E., Reddy, S. M., Coras, R., Aksenov, A. A., Jones, D. R., et al. (2019) · Arthritis & Rheumatology · doi:10.1002/art.41169 · Cited by 82
Maternal aryl hydrocarbon receptor activation protects newborns against necrotizing enterocolitis
Lü, P., Yamaguchi, Y., Fulton, W. B., Wang, S., Zhou, Q., Jia, H., Kovler, M. L., Salazar, A. G., Sampah, M. E., Prindle, T., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-21356-4 · Cited by 79
Kim, K., Srikanth, S., Tan, Y., Yee, M.-K. W., Jew, M., Damoiseaux, R. D., Jung, M. E., Shimizu, S., An, D. S., Ribalet, B., et al. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1302586 · Cited by 81
Antagonism of Aryl Hydrocarbon Receptor Signaling by 6,2′,4′-Trimethoxyflavone
Murray, I. A., Flaveny, C. A., DiNatale, B. C., Chairo, C. R., Schroeder, J. C., Kusnadi, A. R., & Perdew, G. H. (2009) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.109.158261 · Cited by 78
T helper 17 and T regs: a novel proposed mechanism for NB ‐ UVB in vitiligo
Hegazy, R. A., Fawzy, M. M., Gawdat, H. I., Samir, N., & Rashed, L. A. (2014) · Experimental Dermatology · doi:10.1111/exd.12369 · Cited by 78
Richer, M. J., Lang, M. L., & Butler, N. S. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600847 · Cited by 77
Tudela, H., Claus, S. P., & Saleh, M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.719072 · Cited by 81
Solt, L. A., Kumar, N., He, Y., Kamenecka, T. M., Griffin, P. R., & Burris, T. P. (2012) · ACS Chemical Biology · doi:10.1021/cb3002649 · Cited by 77
Loss and Dysregulation of Th17 Cells during HIV Infection
Bixler, S. L., & Mattapallil, J. J. (2013) · Clinical and Developmental Immunology · doi:10.1155/2013/852418 · Cited by 79
Lipopolysaccharide Binding Protein and Oxidative Stress in a Multiple Sclerosis Model
Escribano, B. M., Medina-Fernández, F. J., Aguilar-Luque, M., Agüera, E., Feijóo, M., García-Maceira, F. I., Lillo, R., Vieyra-Reyes, P., Giraldo, A. I., Luque, E., et al. (2016) · Neurotherapeutics · doi:10.1007/s13311-016-0480-0 · Cited by 77
The aryl hydrocarbon receptor: a regulator of Th17 and Treg cell development in disease
Ho, P. P.-K., & Steinman, L. (2008) · Cell Research · doi:10.1038/cr.2008.63 · Cited by 78
Sugimoto, K., Ikeya, K., Bamba, S., Andoh, A., Yamasaki, H., Mitsuyama, K., Nasuno, M., Tanaka, H., Matsuura, A., Kato, M., et al. (2020) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjaa097 · Cited by 76
Th17 cell pathogenicity in autoimmune disease
Park, E., & Ciofani, M. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01535-9 · Cited by 75
Resveratrol, Potential Therapeutic Interest in Joint Disorders: A Critical Narrative Review
Nguyen, C., Savouret, J., Widerak, M., Corvol, M. T., & Rannou, F. (2017) · Nutrients · doi:10.3390/nu9010045 · Cited by 75
Regulation of Innate Lymphoid Cells by Aryl Hydrocarbon Receptor
Li, S., Bostick, J. W., & Zhou, L. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01909 · Cited by 81
Reciprocal transcription factor networks govern tissue-resident ILC3 subset function and identity
Fiancette, R., Finlay, C. M., Willis, C., Bevington, S. L., Soley, J. K., Ng, S. T. H., Baker, S. M., Andrews, S., Hepworth, M. R., & Withers, D. R. (2021) · Nature Immunology · doi:10.1038/s41590-021-01024-x · Cited by 76
O’Driscoll, C. A., Gallo, M. E., Hoffmann, E. J., Fechner, J. H., Schauer, J. J., Bradfield, C. A., & Mezrich, J. D. (2018) · PLOS ONE · doi:10.1371/journal.pone.0209690 · Cited by 74
Natural and inducible TH17 cells are regulated differently by Akt and mTOR pathways
Kim, J. S., Sklarz, T., Banks, L. B., Gohil, M., Waickman, A. T., Skuli, N., Krock, B. L., Luo, C. T., Hu, W., Pollizzi, K. N., et al. (2013) · Nature Immunology · doi:10.1038/ni.2607 · Cited by 80
RetractedBergander, L. V., Cai, W., Klocke, B., Seifert, M., & Pongratz, I. (2012) · Molecular Endocrinology · doi:10.1210/me.2011-1351 · Cited by 74
Manipulation of epithelial integrity and mucosal immunity by host and microbiota‐derived metabolites
Kayama, H., & Takeda, K. (2020) · European Journal of Immunology · doi:10.1002/eji.201948478 · Cited by 77
T helper 17 cells: discovery, function, and physiological trigger
Torchinsky, M. B., & Blander, J. M. (2010) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-009-0248-3 · Cited by 79
Regulation and function of innate and adaptive interleukin‐17‐producing cells
Hirota, K., Ahlfors, H., Duarte, J. H., & Stockinger, B. (2011) · EMBO Reports · doi:10.1038/embor.2011.248 · Cited by 75
Self-citationvan den Hoogen, W., Laman, J. D., & Hart, B. A. ‘. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01081 · Cited by 76
Fu, J., Nogueira, S. V., van Drongelen, V., Coit, P., Ling, S., Rosloniec, E. F., Sawalha, A. H., & Holoshitz, J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1722124115 · Cited by 77
The aryl hydrocarbon receptor is a modulator of anti-viral immunity
Head, J. L., & Lawrence, B. P. (2008) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.10.031 · Cited by 80
Signal transduction and Th17 cell differentiation
O'Shea, J. J., Steward-Tharp, S. M., Laurence, A., Watford, W. T., Wei, L., Adamson, A. S., & Fan, S. (2009) · Microbes and Infection · doi:10.1016/j.micinf.2009.04.007 · Cited by 73
Nakagome, K., Imamura, M., Kawahata, K., Harada, H., Okunishi, K., Matsumoto, T., Sasaki, O., Tanaka, R., Kano, M. R., Chang, H., et al. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1001560 · Cited by 76
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 74
Life, death, and miracles: T h17 cells in the intestine
Huber, S., Gagliani, N., & Flavell, R. A. (2012) · European Journal of Immunology · doi:10.1002/eji.201242619 · Cited by 78
Matthews, N. C., Pfeffer, P., Mann, E. H., Kelly, F. J., Corrigan, C. J., Hawrylowicz, C. M., & Lee, T. H. (2015) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2015-0084oc · Cited by 77
Regulation and function of IL-17A- and IL-22-producing γδ T cells
Ness-Schwickerath, K. J., & Morita, C. T. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0700-z · Cited by 79
The dioxin receptor has tumor suppressor activity in melanoma growth and metastasis
Contador-Troca, M., Alvarez, A. M., Barrasa, E., Rico-Leo, E. M., Catalina‐Fernández, I., Menacho-Márquez, M., Bustelo, X. R., García-Borrón, J. C., Gómez-Durán, Á., Sáenz‐Santamaría, J., et al. (2013) · Carcinogenesis · doi:10.1093/carcin/bgt248 · Cited by 76
IL-17/Th17 mediated synovial inflammation is IL-22 independent
van Hamburg, J. P., Corneth, O. B. J., Paulissen, S. M. J., Davelaar, N., Asmawidjaja, P. S., Mus, A. M. C., & Lubberts, E. (2013) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2012-202373 · Cited by 72
Yan, X., Yan, J., Xiang, Q., Wang, F., Dai, H., Huang, K., Fang, L., Yao, H., Wang, L., & Zhang, W. (2021) · Food & Function · doi:10.1039/d0fo03371e · Cited by 72
Differentiation and function of pro-inflammatory Th17 cells
Dong, C. (2009) · Microbes and Infection · doi:10.1016/j.micinf.2009.04.001 · Cited by 73
Controlling Viral Immuno-Inflammatory Lesions by Modulating Aryl Hydrocarbon Receptor Signaling
Veiga‐Parga, T., Suryawanshi, A. S., & Rouse, B. T. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002427 · Cited by 74
Kimura, A., Abe, H., Tsuruta, S., Chiba, S., Fujii‐Kuriyama, Y., Sekiya, T., Morita, R., & Yoshimura, A. (2013) · International Immunology · doi:10.1093/intimm/dxt067 · Cited by 77
Miller, A. P., Coronel, J., & Amengual, J. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2020.158635 · Cited by 72
c-MAF, a Swiss Army Knife for Tolerance in Lymphocytes
Imbratta, C., Hussein, H., Andris, F., & Verdeil, G. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00206 · Cited by 79
Park, J., Jeong, S.-Y., Choi, A.-J., & Kim, S.-J. (2015) · Immunology Letters · doi:10.1016/j.imlet.2015.03.003 · Cited by 71
Gómez-Durán, Á., Carvajal-González, J. M., Mulero‐Navarro, S., Santiago‐Josefat, B., Puga, A., & Fernández‐Salguero, P. M. (2008) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.08.032 · Cited by 73
Toxicology mechanism of the persistent organic pollutants (POPs) in fish through AhR pathway
Zhou, H., Wu, H., Liao, C., Diao, X., Jiping, Z., Chen, L., & Xue, Q. (2010) · Toxicology Mechanisms and Methods · doi:10.3109/15376516.2010.485227 · Cited by 71
Turski, W. A., Wnorowski, A., Turski, G. N., Turski, C. A., & Turski, L. (2020) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-201042 · Cited by 73
Postbiotic-Enabled Targeting of the Host-Microbiota-Pathogen Interface: Hints of Antibiotic Decline?
Puccetti, M., Xiroudaki, S., Ricci, M., & Giovagnoli, S. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12070624 · Cited by 59
The Rigid Amphipathic Fusion Inhibitor dUY11 Acts through Photosensitization of Viruses
Vigant, F., Hollmann, A., Lee, J., Santos, N. C., Jung, M. E., & Lee, B. (2013) · Journal of Virology · doi:10.1128/jvi.02907-13 · Cited by 70
Regulation of interleukin-10 and interleukin-22 expression in T helper cells
Rutz, S., & Ouyang, W. (2011) · Current Opinion in Immunology · doi:10.1016/j.coi.2011.07.018 · Cited by 77
The impacts of organochlorines and other persistent pollutants on thyroid and metabolic health
Langer, P. (2010) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2010.08.001 · Cited by 73
Dagur, P. K., Biancotto, A., Wei, L., Sen, H. N., Yao, M. D., Strober, W., Nussenblatt, R. B., & McCoy, J. P. (2011) · Journal of Autoimmunity · doi:10.1016/j.jaut.2011.09.003 · Cited by 72
Inoue, H., Mishima, K., Yamamoto-Yoshida, S., Ushikoshi‐Nakayama, R., Nakagawa, Y., Yamamoto, K., Ryo, K., Ide, F., & Saito, I. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1101575 · Cited by 71
Jin, U.-H., Kim, S.-B., & Safe, S. H. (2015) · Chemical Research in Toxicology · doi:10.1021/tx5005198 · Cited by 73
Manipulating Microbiota to Treat Atopic Dermatitis: Functions and Therapies
Alam, J., Xie, L., Yap, Y. A., Marques, F. Z., & Robert, R. (2022) · Pathogens · doi:10.3390/pathogens11060642 · Cited by 71
Pinto, C. J. G., Ávila‐Gálvez, M. Á., Lian, Y., Moura‐Alves, P., & dos Santos, C. N. (2023) · Redox Biology · doi:10.1016/j.redox.2023.102622 · Cited by 73
Tobacco smoke is related to Th17 generation with clinical implications for psoriasis patients
Torii, K., Saito, C., Furuhashi, T., Nishioka, A., Shintani, Y., Kawashima, K., Kato, H., & Morita, A. (2011) · Experimental Dermatology · doi:10.1111/j.1600-0625.2010.01224.x · Cited by 71
Th17 Differentiation and Their Pro-inflammation Function
Song, X., Gao, H., & Qian, Y. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-94-017-9487-9_5 · Cited by 70
Esser, C. (2008) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.10.002 · Cited by 74
Schallreuter, K. U., Salem, M. A. E. L., Gibbons, N. C. J., Maitland, D. J., Marsch, E., Elwary, S. M., & Healey, A. (2012) · The FASEB Journal · doi:10.1096/fj.11-201897 · Cited by 69
The panoply of αβT cells in the skin
Nomura, T., Kabashima, K., & Miyachi, Y. (2014) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2014.07.010 · Cited by 69
Role of Th17 Cytokines in Airway Remodeling in Asthma and Therapy Perspectives
Margelidon-Cozzolino, V., Tsicopoulos, A., Chenivesse, C., & de Nadaı̈, P. (2022) · Frontiers in Allergy · doi:10.3389/falgy.2022.806391 · Cited by 68
Singh, K. P., Bennett, J. A., Casado, F. L., Walrath, J. L., Welle, S. L., & Gasiewicz, T. A. (2013) · Stem Cells and Development · doi:10.1089/scd.2013.0346 · Cited by 71
AhR protein trafficking and function in the skin
Ikuta, T., Namiki, T., Fujii-Kuriyama, Y., & Kawajiri, K. (2009) · Biochemical Pharmacology · doi:10.1016/j.bcp.2008.10.003 · Cited by 68
Mastelic, B., do Rosário, A. P. F., Veldhoen, M., Renauld, J., Jarra, W., Sponaas, A., Roetynck, S., Stockinger, B., & Langhorne, J. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00085 · Cited by 68
Self-citationTryptophan metabolites kynurenine and serotonin regulate fibroblast activation and fibrosis
Dolivo, D., Larson, S. A., & Dominko, T. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2880-2 · Cited by 71
Aryl hydrocarbon receptor (AhR) ligands as selective AhR modulators: Genomic studies
Safe, S. H., Han, H., Goldsby, J. S., Mohankumar, K., & Chapkin, R. S. (2018) · Current Opinion in Toxicology · doi:10.1016/j.cotox.2018.11.005 · Cited by 70
Vuerich, M., Harshe, R. P., Frank, L. A., Mukherjee, S., Gromová, B., Csizmadia, E., Nasser, I. A., Ma, Y., Bonder, A., Patwardhan, V. R., et al. (2020) · Journal of Hepatology · doi:10.1016/j.jhep.2020.06.044 · Cited by 70
Targeting AhR as a Novel Therapeutic Modality against Inflammatory Diseases
Cannon, A. S., Nagarkatti, P. S., & Nagarkatti, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010288 · Cited by 72
Development of Novel CH223191-Based Antagonists of the Aryl Hydrocarbon Receptor
Choi, E.-Y., Lee, H., Dingle, R. W. C., Kim, K. B., & Swanson, H. I. (2011) · Molecular Pharmacology · doi:10.1124/mol.111.073643 · Cited by 68
Transcriptional Regulatory Networks for CD4 T Cell Differentiation
Christie, D. A., & Zhu, J. (2014) · Current topics in microbiology and immunology · doi:10.1007/82_2014_372 · Cited by 69
Autonomic dysfunction, immune regulation, and multiple sclerosis
Racosta, J. M., & Kimpinski, K. (2015) · Clinical Autonomic Research · doi:10.1007/s10286-015-0325-7 · Cited by 67
Hasselmann, J., Karim, H., Khalaj, A. J., Ghosh, S., & Tiwari-Woodruff, S. K. (2017) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2017.04.003 · Cited by 70
Lin, Y., Luck, H., Khan, S. M., Schneeberger, P. H. H., Tsai, S. J., Clemente‐Casares, X., Lei, H., Leu, Y., Chan, Y. T., Chen, H., et al. (2019) · International Journal of Obesity · doi:10.1038/s41366-019-0340-1 · Cited by 73
Role of IL-22 in homeostasis and diseases of the skin
Lopez, D. V., & Kongsbak‐Wismann, M. (2022) · Apmis · doi:10.1111/apm.13221 · Cited by 66
Translational Mini-Review Series on Th17 Cells: Development of mouse and human T helper 17 cells
de Jong, E. C., Suddason, T., & Lord, G. M. (2009) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2009.04041.x · Cited by 67
Vonarbourg, C., & Diefenbach, A. (2012) · Seminars in Immunology · doi:10.1016/j.smim.2012.03.002 · Cited by 72
Cellular Plasticity of CD4+ T Cells in the Intestine
Brucklacher-Waldert, V., Carr, E. J., Linterman, M. A., & Veldhoen, M. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00488 · Cited by 70
Self-citationNoakes, R. (2015) · International Journal of Tryptophan Research · doi:10.4137/ijtr.s19985 · Cited by 68
Mechanisms underlying lineage commitment and plasticity of human γδ T cells
Caccamo, N., Todaro, M., Sireci, G., Meraviglia, S., Stassi, G., & Dieli, F. (2012) · Cellular and Molecular Immunology · doi:10.1038/cmi.2012.42 · Cited by 69
Min, H. K., Kim, S., Baek, S.-Y., Woo, J., Park, J., Cho, M., Lee, J. J., Kwok, S., Kim, S. W., & Park, S. (2015) · PLoS ONE · doi:10.1371/journal.pone.0138201 · Cited by 66
TH17 Cell and Epithelial Cell Crosstalk during Inflammatory Bowel Disease and Carcinogenesis
Kempski, J., Brockmann, L., Gagliani, N., & Huber, S. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01373 · Cited by 66
Aryl hydrocarbon receptor: The master regulator of immune responses in allergic diseases
Riaz, F., Pan, F., & Wei, P. Y. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1057555 · Cited by 73
Miao, T., Raymond, M., Bhullar, P., Ghaffari, E., Symonds, A. L. J., Meier, U., Giovannoni, G., Li, S., & Wang, P. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1200868 · Cited by 65
Kado, S. Y., Chang, W. L. W., Nguyen, A., Wolny, M., Shepherd, D. M., & Vogel, C. F. A. (2016) · Archives of Toxicology · doi:10.1007/s00204-016-1880-y · Cited by 68
Gargaro, M., Manni, G., Scalisi, G., Puccetti, P., & Fallarino, F. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094644 · Cited by 66
Helper T Cell Plasticity: Impact of Extrinsic and Intrinsic Signals on Transcriptomes and Epigenomes
Bonelli, M. M., Shih, H., Hirahara, K., Singelton, K., Laurence, A. D. J., Poholek, A. C., Hand, T., Mikami, Y., Vahedi, G., Kanno, Y., et al. (2014) · Current topics in microbiology and immunology · doi:10.1007/82_2014_371 · Cited by 66
Wheeler, J. L. H., Martin, K. C., Resseguie, E. A., & Lawrence, B. P. (2013) · Toxicological Sciences · doi:10.1093/toxsci/kft255 · Cited by 67
Brandstätter, O., Schanz, O., Vorac, J., König, J., Mori, T., Maruyama, T., Korkowski, M., Haarmann‐Stemmann, T., von Smolinski, D., Schultze, J. L., et al. (2016) · Scientific Reports · doi:10.1038/srep26091 · Cited by 65
Host-microbiome interactions: the aryl hydrocarbon receptor and the central nervous system
Lee, H. U., McPherson, Z. E., Tan, B., Korecka, A., & Pettersson, S. (2016) · Journal of Molecular Medicine · doi:10.1007/s00109-016-1486-0 · Cited by 65
Indoleamine 2,3-dioxygenase 1 (IDO1) inhibitors activate the aryl hydrocarbon receptor
Moyer, B. J., Rojas, I. Y., Murray, I. A., Lee, S., Hazlett, H. F., Perdew, G. H., & Tomlinson, C. R. (2017) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2017.03.012 · Cited by 65
Luecke-Johansson, S., Gralla, M., Rundqvist, H., Ho, J. C., Johnson, R. S., Gradin, K., & Poellinger, L. (2017) · Molecular and Cellular Biology · doi:10.1128/mcb.00630-16 · Cited by 68
Furness, S. G. B., & Whelan, F. (2009) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2009.09.004 · Cited by 63
Aryl hydrocarbon receptor and experimental autoimmune arthritis
Nguyen, N. T., Nakahama, T., & Kishimoto, T. (2013) · Seminars in Immunopathology · doi:10.1007/s00281-013-0392-6 · Cited by 66
Osteoclasts in arthritis and Th17 cell development
Okamoto, K., & Takayanagi, H. (2010) · International Immunopharmacology · doi:10.1016/j.intimp.2010.11.010 · Cited by 66
Metadata
- Authors
- Veldhoen, M., Hirota, K., Westendorf, A. M., Buer, J., Dumoutier, L., Renauld, J.-C., & Stockinger, B.
- Affiliations
- National Institute for Medical Research (GB)
- Essen University Hospital (DE)
- Ludwig Cancer Research (BE)
- Corresponding author
- Stockinger, Brigitta
- ORCID
- Venue
- Nature
- Published
- 2008-03-23
- Volume
- 453
- Issue
- 7191
- Pages
- 106-109
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W1993003564
- Cited by
- 1,634
- References
- 31
- Citations by year
- 2026: 33 · 2025: 44 · 2024: 49 · 2023: 54 · 2022: 87 · 2021: 94 · 2020: 96 · 2019: 90 · 2018: 96 · 2017: 93 · 2016: 96 · 2015: 82 · 2014: 114 · 2013: 107 · 2012: 118
- FWCI
- 52.43
- Type
- journal article
- Language
- en
- Open access
- green
- hdl.handle.net
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- HZI (Helmholtz Centre for Infection Research) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DIAL (Catholic University of Leuven) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- University of Leicester
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Immunotoxicology and immune responses
- Keywords
- aryl hydrocarbon receptor, Th17 cells, autoimmunity, environmental toxins, IL-22, experimental autoimmune encephalitis, multiple sclerosis, regulatory T cells, CD4+ T cells, immunomodulation, AhR ligands, dioxins, IL-17
- MeSH terms
- Interleukin-22, Animals, Cell Differentiation, Cells, Cultured, Encephalomyelitis, Autoimmune, Experimental, Environmental Exposure, Environmental Pollutants, T-Lymphocytes, Helper-Inducer, Humans, Interleukins, Ligands, Mice, Inbred C57BL, Transduction, Genetic, Hazardous Substances, Autoimmunity, Receptors, Aryl Hydrocarbon, Interleukin-17, Mice
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