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The aryl hydrocarbon receptor: an environmental sensor integrating immune responses in health and disease
Abstract
The environment, diet, microbiota and body's metabolism shape complex biological processes in health and disease. However, our understanding of the molecular pathways involved in these processes is still limited. The aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor that integrates environmental, dietary, microbial and metabolic cues to control complex transcriptional programmes in a ligand-specific, cell-type-specific and context-specific manner. In this Review, we summarize our current knowledge of AHR and the transcriptional programmes it controls in the immune system. Finally, we discuss the role of AHR in autoimmune and neoplastic diseases of the central nervous system, with a special focus on the gut immune system, the gut-brain axis and the therapeutic potential of targeting AHR in neurological disorders.
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“AhR, a ligand-dependent transcription factor, can be activated by diverse ligands including indole-based compounds (22, 23).”
From Sepsis-Induced Gut Dysbiosis Mediates the Susceptibility to Sepsis-Associated Encephalopathy in Mice (2022) · cites this paper as [22]
In the citing paper
“The GI microbiome is thought to be a key player in this process as it is essential for the proper maintenance of the intestinal barrier through various mechanisms, e.g., production of SCFA (Bron et al., 2017) as well as tryptophan metabolites (Rothhammer and Quintana, 2019).”
From Viral Infections, the Microbiome, and Probiotics (2021) · cites this paper as Rothhammer and Quintana, 2019
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Cites
Neurotoxic reactive astrocytes are induced by activated microglia
Liddelow, S. A., Guttenplan, K. A., Clarke, L. E., Bennett, F. C., Bohlen, C. J., Schirmer, L., Bennett, M. L., Münch, A. E., Chung, W.-S., Peterson, T. C., et al. (2017) · Nature · doi:10.1038/nature21029 · Cited by 7,971
Gut microbiota regulate motor deficits and neuroinflammation in a model of Parkinson's disease
Sampson, T. R., Debelius, J. W., Thron, T., Janssen, S., Shastri, G. G., Ilhan, Z. E., Challis, C., Schretter, C. E., Rocha, S., Gradinaru, V., et al. (2016) · Cell · doi:10.1016/j.cell.2016.11.018 · Cited by 3,622
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
Host microbiota constantly control maturation and function of microglia in the CNS
Erny, D., Hrabě de Angelis, A. L., Jaitin, D., Wieghofer, P., Staszewski, O., David, E., Keren-Shaul, H., Mahlakoiv, T., Jakobshagen, K., Buch, T., et al. (2015) · Nature Neuroscience · doi:10.1038/nn.4030 · Cited by 3,569
Microglia Function in the Central Nervous System During Health and Neurodegeneration
Colonna, M., & Butovsky, O. (2017) · Annual Review of Immunology · doi:10.1146/annurev-immunol-051116-052358 · Cited by 2,894
Metabolomics analysis reveals large effects of gut microflora on mammalian blood metabolites
Wikoff, W. R., Anfora, A. T., Liu, J., Schultz, P. G., Lesley, S. A., Peters, E. C., & Siuzdak, G. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0812874106 · Cited by 2,677
Zelante, T., Iannitti, R. G., Cunha, C., De Luca, A., Giovannini, G., Pieraccini, G., Zecchi, R., D’Angelo, C., Massi-Benedetti, C., Fallarino, F., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.08.003 · Cited by 2,614
An endogenous tumour-promoting ligand of the human aryl hydrocarbon receptor
Opitz, C. A., Litzenburger, U. M., Sahm, F., Ott, M., Tritschler, I., Trump, S., Schumacher, T., Jestaedt, L., Schrenk, D., Weller, M., et al. (2011) · Nature · doi:10.1038/nature10491 · Cited by 1,898
IL-21 initiates an alternative pathway to induce proinflammatory TH17 cells
Korn, T., Bettelli, E., Gao, W., Awasthi, A., Jäger, A., Strom, T. B., Oukka, M., & Kuchroo, V. K. (2007) · Nature · doi:10.1038/nature05970 · Cited by 1,896
Denison, M. S., & Nagy, S. R. (2003) · Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.43.100901.135828 · Cited by 1,895
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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
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Sadik, A., Patterson, L. F. S., Öztürk, S., Mohapatra, S. R., Panitz, V., Secker, P. F., Pfänder, P., Loth, S., Salem, H., Prentzell, M. T., et al. (2020) · Cell · doi:10.1016/j.cell.2020.07.038 · Cited by 585
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Vogel, C. F. A., Winkle, L. S. V., Esser, C., & Haarmann‐Stemmann, T. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101530 · Cited by 538
Hays, K. E., Pfaffinger, J. M., & Ryznar, R. J. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2393270 · Cited by 541
Inhibition and induction of CYP enzymes in humans: an update
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Liu, Y., Zhou, N., Zhou, L., Wang, J., Zhou, Y., Zhang, T., Fang, Y., Deng, J., Gao, Y., Liang, X., et al. (2021) · Nature Immunology · doi:10.1038/s41590-020-00850-9 · Cited by 372
Aburto, M. R., & Cryan, J. F. (2024) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-023-00890-0 · Cited by 407
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Obata, Y., Castaño, Á., Boeing, S., Bon‐Frauches, A. C., Fung, C., Fallesen, T. L., de Agüero, M. G., Yılmaz, B., Lopes, R., Huseynova, A., et al. (2020) · Nature · doi:10.1038/s41586-020-1975-8 · Cited by 365
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Wu, K., Yuan, Y., Yu, H., Dai, X., Wang, S., Sun, Z., Wang, F., Fei, H., Lin, Q., Jiang, H., et al. (2020) · Blood · doi:10.1182/blood.2019003990 · Cited by 345
Molecular mechanisms of oxidative stress in asthma
Michaeloudes, C., Abubakar-Waziri, H., Lakhdar, R., Raby, K., Dixey, P., Adcock, I. M., Mumby, S. E., Bhavsar, P. K., & Chung, K. F. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2021.101026 · Cited by 348
The therapeutic potential of targeting tryptophan catabolism in cancer
Opitz, C. A., Somarribas Patterson, L. F., Mohapatra, S. R., Dewi, D. L., Sadik, A., Platten, M., & Trump, S. (2020) · British Journal of Cancer · doi:10.1038/s41416-019-0664-6 · Cited by 300
High-fat diet-induced upregulation of exosomal phosphatidylcholine contributes to insulin resistance
Kumar, A., Sundaram, K., Mu, J., Dryden, G. W., Sriwastva, M. K., Lei, C., Zhang, L., Qiu, X., Xu, F., Yan, J., et al. (2021) · Nature Communications · doi:10.1038/s41467-020-20500-w · Cited by 276
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Sun, J., Zhang, Y., Kong, Y., Ye, T., Yu, Q., Kumaran Satyanarayanan, S., Su, K.-P., & Liu, J. (2022) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2022.08.003 · Cited by 255
Zhang, Z., Tang, H., Chen, P., Xie, H., & Tao, Y. (2019) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-019-0074-5 · Cited by 263
Intestinal microbiota-derived tryptophan metabolites are predictive of Ah receptor activity
Dong, F., Hao, F., Murray, I. A., Smith, P. B. W., Koo, I., Tindall, A. M., Kris‐Etherton, P. M., Gowda, K., Amin, S., Patterson, A. D., et al. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1788899 · Cited by 252
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Patterson, A., Rimal, B., Collins, S., Granda, M., Koo, I., Solanka, S., Hoque, N., Gentry, E., Yan, T., Bisanz, J., et al. (2022) · doi:10.21203/rs.3.rs-2050120/v1 · Cited by 252
Tryptophan metabolism drives dynamic immunosuppressive myeloid states in IDH-mutant gliomas
Friedrich, M., Sankowski, R., Bunse, L., Kilian, M., Green, E., Guevara, C. R., Pusch, S., Poschet, G., Sanghvi, K., Hahn, M., et al. (2021) · Nature Cancer · doi:10.1038/s43018-021-00201-z · Cited by 241
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Gutiérrez‐Castrellón, P., Gandara-Martí, T., y Abreu, A. T. A., Nieto-Rufino, C. D., López-Orduña, E., Jiménez–Escobar, I., Jiménez-Gutiérrez, C., López‐Velázquez, G., & Espadaler, J. (2022) · Gut Microbes · doi:10.1080/19490976.2021.2018899 · Cited by 220
Simon, E., Călinoiu, L. F., Mitrea, L., & Vodnar, D. C. (2021) · Nutrients · doi:10.3390/nu13062112 · Cited by 235
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Shi, D., Wu, X., Jian, Y., Wang, J., Huang, C., Mo, S., Li, Y., Li, F., Zhang, C., Zhang, D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33285-x · Cited by 221
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Self-citationPeng, B., Dong, Q., Li, F., Wang, T., Qiu, X., & Zhu, T. (2023) · Environmental Science & Technology · doi:10.1021/acs.est.3c03170 · Cited by 209
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Self-citationFunctions of the aryl hydrocarbon receptor (AHR) beyond the canonical AHR/ARNT signaling pathway
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Lamas, B., Hernandez-Galan, L., Galipeau, H. J., Constante, M., Clarizio, A., Jury, J., Breyner, N. M., Caminero, A., Rueda, G., Hayes, C. L., et al. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aba0624 · Cited by 179
Garlic exosome-like nanoparticles reverse high-fat diet induced obesity via the gut/brain axis
Sundaram, K., Mu, J., Kumar, A., Behera, J., Lei, C., Sriwastva, M. K., Xu, F., Dryden, G. W., Zhang, L., Chen, S., et al. (2022) · Theranostics · doi:10.7150/thno.65427 · Cited by 186
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Espi, M., Koppe, L., Fouque, D. P., & Thaunat, O. (2020) · Toxins · doi:10.3390/toxins12050300 · Cited by 195
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Panda, S. K., Peng, V., Sudan, R., Ulezko Antonova, A., Di Luccia, B., Ohara, T. E., Fachi, J. L., Grajales-Reyes, G. E., Jaeger, N., Trsan, T., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.01.023 · Cited by 174
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Furue, M. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9113741 · Cited by 161
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Török, N., Tanaka, M., & Vécsei, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249338 · Cited by 154
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Self-citationNutritional regulation of microbiota-derived metabolites: Implications for immunity and inflammation
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Fournier, E., Leveque, M., Ruiz, P., Ratel, J., Durif, C., Chalançon, S., Amiard, F., Edely, M., Bézirard, V., Gaultier, E., et al. (2022) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2022.130010 · Cited by 165
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Lai, W., Deng, W.-F., Xu, S., Zhao, J., Xu, D., Liu, Y., Guo, Y., Wang, M., He, F.-S., Ye, S.-W., et al. (2019) · Psychological Medicine · doi:10.1017/s0033291719003027 · Cited by 143
Therapeutic induction of antigen-specific immune tolerance
Kenison, J. E., Stevens, N. A., & Quintana, F. J. (2023) · Nature reviews. Immunology · doi:10.1038/s41577-023-00970-x · Cited by 162
Self-citationTang, S., Liu, W., Zhao, Q., Li, K., Zhu, J., Yao, W., & Gao, X. (2020) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.113280 · Cited by 147
Carrillo-Salinas, F. J., Anastasiou, M., Ngwenyama, N., Kaur, K., Tai, A., Smolgovsky, S. A., Jetton, D., Aronovitz, M. J., & Alcaide, P. (2020) · Gut Microbes · doi:10.1080/19490976.2020.1823801 · Cited by 146
Zhao, C., Hu, X., Bao, L., Wu, K., Feng, L., Qiu, M., Hao, H., Fu, Y., & Zhang, N. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009774 · Cited by 146
Epithelial cells: liaisons of immunity
Larsen, S. B., Cowley, C. J., & Fuchs, E. V. (2019) · Current Opinion in Immunology · doi:10.1016/j.coi.2019.11.004 · Cited by 153
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Duess, J. W., Sampah, M. E., Lopez, C. M., Tsuboi, K., Scheese, D. J., Sodhi, C. P., & Hackam, D. J. (2023) · Gut Microbes · doi:10.1080/19490976.2023.2221470 · Cited by 153
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Vı́tek, L. (2020) · Medicinal Research Reviews · doi:10.1002/med.21660 · Cited by 136
Li, K., Hao, Z., Du, J., Gao, Y., Yang, S., & Zhou, Y. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.107183 · Cited by 134
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Planas, A. M. (2024) · Glia · doi:10.1002/glia.24501 · Cited by 144
Lin, H., Buerki‐Thurnherr, T., Kaur, J., Wick, P., Pelin, M., Tubaro, A., Carniel, F. C., Tretiach, M., Emmanuel Flahaut, B., Iglesias, D., et al. (2024) · ACS Nano · doi:10.1021/acsnano.3c09699 · Cited by 136
Grishanova, A. Y., & Perepechaeva, M. L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23126719 · Cited by 130
Tryptophan metabolism: Mechanism-oriented therapy for neurological and psychiatric disorders
Li, D., Yu, S., Long, Y., Shi, A., Deng, J., Ma, Y., Wen, J., Li, X., Liu, S., Zhang, Y., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.985378 · Cited by 129
Martin, K. S., Azzolini, M., & Ruas, J. L. (2020) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00580.2019 · Cited by 128
The Microbial Pecking Order: Utilization of Intestinal Microbiota for Poultry Health
Maki, J. J., Klima, C. L., Sylte, M. J., & Looft, T. P. (2019) · Microorganisms · doi:10.3390/microorganisms7100376 · Cited by 130
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Peyraud, F., Guégan, J., Bodet, D., Cousin, S., Bessede, A., & Italiano, A. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.807271 · Cited by 137
Tang, Z., Bai, Y., Fang, Q., Yuan, Y., Zeng, Q., Chen, S., Xu, T., Chen, J., Tan, L., Wang, C., et al. (2025) · Cancer Cell · doi:10.1016/j.ccell.2025.03.011 · Cited by 138
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Descamps, H. C., Herrmann, B. I., Wiredu, D., & Thaiss, C. A. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.05.063 · Cited by 123
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Sanmarco, L. M., Polonio, C. M., Wheeler, M. A., & Quintana, F. J. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20202715 · Cited by 134
Self-citationEndothelial AHR activity prevents lung barrier disruption in viral infection
Major, J., Crotta, S., Finsterbusch, K., Chakravarty, P., Shah, K., Frederico, B., D’Antuono, R., Green, M. J., Meader, L., Suárez‐Bonnet, A., et al. (2023) · Nature · doi:10.1038/s41586-023-06287-y · Cited by 127
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Wang, T., Chen, B., Luo, M., Xie, L., Lu, M., Lu, X., Zhang, S., Wei, L., Zhou, X., Yao, B., et al. (2023) · Microbiome · doi:10.1186/s40168-023-01656-1 · Cited by 118
“GrimAge,” an epigenetic predictor of mortality, is accelerated in major depressive disorder
Protsenko, E., Yang, R., Nier, B., Reus, V. I., Hammamieh, R., Rampersaud, R., Wu, G. W. Y., Hough, C. M., Epel, E. S., Prather, A. A., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01302-0 · Cited by 118
Greathouse, K. L., & Wyatt, M. (2021) · Nutrients · doi:10.3390/nu13041189 · Cited by 116
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Metadata
- Authors
- Rothhammer, V., & Quintana, F. J.
- Affiliations
- Brigham and Women's Hospital (US)
- Corresponding author
- Quintana, Francisco J.
- Venue
- Nature Reviews Immunology
- Published
- 2019-02-04
- Volume
- 19
- Issue
- 3
- Pages
- 184-197
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- OpenAlex
- W2911968308
- Cited by
- 1,197
- References
- 207
- Citations by year
- 2026: 148 · 2025: 189 · 2024: 179 · 2023: 192 · 2022: 173 · 2021: 160 · 2020: 117 · 2019: 37
- FWCI
- 11.68
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- mediaTUM – the media and publications repository of the Technical University Munich (Technical University Munich) (submittedVersion)
- Topics
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Toxic Organic Pollutants Impact
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Receptors and Signaling
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics, phytochemicals, and oxidative stress
- Keywords
- aryl hydrocarbon receptor, environmental sensing, immune regulation, gut immune system, gut-brain axis, autoimmune disease, central nervous system tumors, transcriptional programs, microbiota, neurological disorders
- MeSH terms
- Gastrointestinal Microbiome, Animals, Brain, Diet, Environment, Gene Expression Regulation, Humans, Intestines, Signal Transduction, Receptors, Aryl Hydrocarbon, Autoimmune Diseases of the Nervous System, Adaptive Immunity, Molecular Targeted Therapy, Microbiota
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