P. Alonso-magdalena, E. Vieira, S. Soriano, L. Menes, D. Burks et al., Bisphenol A exposure during pregnancy disrupts glucose homeostasis in mothers and adult male offspring, Environ. Health Perspect, vol.118, pp.1243-1250, 2010.

G. Andújar, R. Zafra-gómez, . Álvarez-cubero, . Aguilera, and R. Monteagudo, Bisphenol A Analogues in Food and Their Hormonal and Obesogenic Effects: A Review, Nutrients, vol.11, 2019.

B. M. Angle, R. P. Do, D. Ponzi, R. W. Stahlhut, B. E. Drury et al., Metabolic disruption in male mice due to fetal exposure to low but not high doses of bisphenol A (BPA): evidence for effects on body weight, food intake, adipocytes, leptin, adiponectin, insulin and glucose regulation, Reprod. Toxicol, vol.42, pp.256-268, 2013.

E. Baricza, V. Tamási, N. Marton, E. I. Buzás, and G. Nagy, The emerging role of aryl hydrocarbon receptor in the activation and differentiation of Th17 cells, Cell. Mol. Life Sci, vol.73, pp.95-117, 2016.

S. M. Bauer, A. Roy, J. Emo, T. J. Chapman, S. N. Georas et al., The effects of maternal exposure to bisphenol A on allergic lung inflammation into adulthood, Toxicol Sci, vol.130, pp.82-93, 2012.

C. Beausoleil, C. Emond, J. Cravedi, J. Antignac, M. Applanat et al., Regulatory identification of BPA as an endocrine disruptor: Context and methodology, Molecular and Cellular Endocrinology, vol.475, pp.4-9, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01864338

R. Becher, H. Wellendorf, A. K. Sakhi, J. T. Samuelsen, C. Thomsen et al., Presence and leaching of bisphenol a (BPA) from dental materials, Acta Biomater Odontol Scand, vol.4, pp.56-62, 2018.

E. C. Bonefeld-jørgensen, M. Long, M. V. Hofmeister, and A. M. Vinggaard, Endocrine-disrupting potential of bisphenol A, bisphenol A dimethacrylate, 4-n-nonylphenol, and 4-n-octylphenol in vitro: new data and a brief review, Environ. Health Perspect, vol.115, pp.69-76, 2007.

V. Braniste, A. Jouault, E. Gaultier, A. Polizzi, C. Buisson-brenac et al., Impact of oral bisphenol A at reference doses on intestinal barrier function and sex differences after perinatal exposure in rats, Proc Natl Acad Sci U S A, vol.107, pp.448-53, 2010.
URL : https://hal.archives-ouvertes.fr/hal-01608653

A. M. Calafat, Z. Kuklenyik, J. A. Reidy, S. P. Caudill, J. Ekong et al., Urinary Concentrations of Bisphenol A and 4-Nonylphenol in a Human Reference Population, Environmental Health Perspectives, vol.113, pp.391-395, 2005.

A. Camarca, C. Gianfrani, F. Ariemma, I. Cimmino, D. Bruzzese et al., Human Peripheral Blood Mononuclear Cell Function and Dendritic Cell Differentiation Are Affected by Bisphenol-A Exposure, PLoS ONE, vol.11, 2016.

X. Cao, I. Kosarac, S. Popovic, S. Zhou, D. Smith et al., LC-MS/MS analysis of bisphenol S and five other bisphenols in total diet food samples, Food Additives & Contaminants: Part A, vol.36, pp.1740-1747, 2019.

L. Cervantes-barragan and M. Colonna, Chemical sensing in development and function of intestinal lymphocytes, Current Opinion in Immunology, vol.50, pp.112-116, 2018.

J. Chen, Y. Xiao, Z. Gai, R. Li, Z. Zhu et al., Reproductive toxicity of low level bisphenol A exposures in a two-generation zebrafish assay: Evidence of male-specific effects, Aquat. Toxicol, vol.169, pp.204-214, 2015.

M. Chen, P. Zhu, B. Xu, R. Zhao, S. Qiao et al., Determination of nine environmental phenols in urine by ultra-highchromatography-tandem mass spectrometry, J Anal Toxicol, vol.36, pp.608-615, 2012.

J. Cho, S. Kim, D. H. Yang, J. Lee, K. W. Park et al., Mucosal Immunity Related to FOXP3+ Regulatory T Cells, Th17 Cells and Cytokines in Pediatric Inflammatory Bowel Disease, J. Korean Med. Sci, vol.33, 2018.

G. Cui, X. Qin, L. Wu, Y. Zhang, X. Sheng et al., Liver X receptor (LXR) mediates negative regulation of mouse and human Th17 differentiation, J. Clin. Invest, vol.121, pp.658-670, 2011.

E. De-filippis, T. Li, and E. D. Rosen, Exposure of adipocytes to bisphenol-A in vitro interferes with insulin action without enhancing adipogenesis, PLoS ONE, vol.13, 2018.

J. A. Deluca, K. F. Allred, R. Menon, R. Riordan, B. R. Weeks et al., Bisphenol-A alters microbiota metabolites derived from aromatic amino acids and worsens disease activity during colitis, Experimental Biology and Medicine, vol.243, pp.864-875, 2018.

K. M. Donohue, R. L. Miller, M. S. Perzanowski, A. C. Just, L. A. Hoepner et al., Prenatal and postnatal bisphenol A exposure and asthma development among inner-city children, Journal of Allergy and Clinical Immunology, vol.131, pp.736-742, 2013.

A. K. Ehrlich, J. M. Pennington, W. H. Bisson, S. K. Kolluri, and N. I. Kerkvliet, TCDD, FICZ, and Other High Affinity AhR Ligands Dose-Dependently Determine the Fate of CD4+ T Cell Differentiation, Toxicological Sciences, vol.161, pp.310-320, 2018.

C. Flaveny, Transgenic Humanized AHR Mouse Reveals Differences between Human and Mouse AHR Ligand Selectivity, Mol Cell Pharmacol, vol.1, pp.119-123, 2009.

M. T. García-córcoles, M. Cipa, R. Rodríguez-gómez, A. Rivas, F. Olea-serrano et al., Determination of bisphenols with estrogenic activity in plastic packaged baby food samples using solid-liquid extraction and clean-up with dispersive sorbents followed by gas chromatography tandem mass spectrometry analysis, Talanta, vol.178, pp.441-448, 2018.

M. Gascon, M. Casas, E. Morales, D. Valvi, A. Ballesteros-gómez et al., Prenatal exposure to bisphenol A and phthalates and childhood respiratory tract infections and allergy, Journal of Allergy and Clinical Immunology, vol.135, pp.370-378, 2015.

J. M. Gostner, E. Raggl, K. Becker, F. Überall, H. Schennach et al., Bisphenol A suppresses Th1-type immune response in human peripheral blood mononuclear cells in vitro, Immunol. Lett, vol.168, pp.285-292, 2015.

M. Grimaldi, A. Boulahtouf, L. Toporova, and P. Balaguer, Functional profiling of bisphenols for nuclear receptors, Toxicology, vol.420, pp.39-45, 2019.
URL : https://hal.archives-ouvertes.fr/hal-02420939

C. Herz, H. T. Tran, N. Schlotz, K. Michels, and E. Lamy, Low-dose levels of bisphenol A inhibit telomerase via ER/GPR30-ERK signalling, impair DNA integrity and reduce cell proliferation in primary PBMC, Sci Rep, vol.7, 2017.

F. Huang, Y. Chang, S. Lee, M. Yang, and Y. Kuan, Expression of pro-inflammatory cytokines and mediators induced by Bisphenol A via ERK-NF?B and JAK1/2-STAT3 pathways in macrophages, Environ. Toxicol, vol.34, pp.486-494, 2019.

C. G. Hurtado, F. Wan, F. Housseau, and C. L. Sears, Roles for Interleukin 17 and Adaptive Immunity in Pathogenesis of Colorectal Cancer, Gastroenterology, vol.155, pp.1706-1715, 2018.

H. Jin, J. Zhu, Z. Chen, Y. Hong, and Z. Cai, Occurrence and Partitioning of Bisphenol Analogues in Adults, Blood from China. Environ. Sci. Technol, vol.52, pp.812-820, 2018.

E. R. Kabir, M. S. Rahman, and I. Rahman, A review on endocrine disruptors and their possible impacts on human health, Environ. Toxicol. Pharmacol, vol.40, pp.241-258, 2015.

S. Kim, E. C. Henry, D. Kim, Y. Kim, K. J. Shin et al., Novel Compound 2-Methyl-2 H -pyrazole-3-carboxylic Acid (2-methyl-4-o -tolylazo-phenyl)-amide (CH-223191) Prevents 2,3,7,8-TCDD-Induced Toxicity by Antagonizing the Aryl Hydrocarbon Receptor, Mol Pharmacol, vol.69, pp.1871-1878, 2006.

N. Kovalova, R. Nault, R. Crawford, T. R. Zacharewski, and N. E. Kaminski, Comparative analysis of TCDD-induced AhR-mediated gene expression in human, mouse and rat primary B cells, Toxicology and Applied Pharmacology, vol.316, pp.95-106, 2017.

T. Krüger, M. Long, and E. C. Bonefeld-jørgensen, Plastic components affect the activation of the aryl hydrocarbon and the androgen receptor, Toxicology, vol.246, pp.112-123, 2008.

F. Lagarde, C. Beausoleil, S. M. Belcher, L. P. Belzunces, C. Emond et al., Non-monotonic dose-response relationships and endocrine disruptors: a qualitative method of assessment, Environmental Health, vol.14, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01151409

M. H. Lee, S. W. Chung, B. Y. Kang, J. Park, C. H. Lee et al., Enhanced interleukin-4 production in CD4+ T cells and elevated immunoglobulin E levels in antigenprimed mice by bisphenol A and nonylphenol, endocrine disruptors: involvement of nuclear factor-AT and Ca2+, Immunology, vol.109, pp.76-86, 2003.

M. Liamin, E. Boutet-robinet, E. L. Jamin, M. Fernier, L. Khoury et al., Benzo[a]pyrene-induced DNA damage associated with mutagenesis in primary human activated T lymphocytes, Biochem. Pharmacol, vol.137, pp.113-124, 2017.
URL : https://hal.archives-ouvertes.fr/hal-01560145

M. Liamin, H. Le-mentec, B. Evrard, L. Huc, F. Chalmel et al., Genome-Wide Transcriptional and Functional Analysis of Human T Lymphocytes Treated with Benzo[?]pyrene, Int J Mol Sci, vol.19, 2018.
URL : https://hal.archives-ouvertes.fr/hal-01940253

C. Liao, F. Liu, Y. Guo, H. Moon, H. Nakata et al., Occurrence of eight bisphenol analogues in indoor dust from the United States and several Asian countries: implications for human exposure, Environ. Sci. Technol, vol.46, pp.9138-9145, 2012.

X. Liu, H. Hu, H. Fan, D. Zuo, Z. Shou et al., The role of STAT3 and AhR in the differentiation of CD4+ T cells into Th17 and Treg cells, 2017.

S. Luo, Y. Li, Y. Li, Q. Zhu, J. Jiang et al., Gestational and lactational exposure to low-dose bisphenol A increases Th17 cells in mice offspring, Environ Toxicol Pharmacol, vol.47, pp.149-158, 2016.

Y. Malaisé, S. Menard, C. Cartier, E. Gaultier, F. Lasserre et al., Gut dysbiosis and impairment of immune system homeostasis in perinatally-exposed mice to Bisphenol A precede obese phenotype development, Sci Rep, vol.7, 2017.

Y. Malaisé, S. Ménard, C. Cartier, C. Lencina, C. Sommer et al., Consequences of bisphenol a perinatal exposure on immune responses and gut in mice, Arch. Toxicol, vol.92, pp.347-358, 2018.

S. Menard, L. Guzylack-piriou, M. Leveque, V. Braniste, C. Lencina et al., Food intolerance at adulthood after perinatal exposure to the endocrine disruptor bisphenol A, FASEB J, vol.28, pp.4893-900, 2014.
URL : https://hal.archives-ouvertes.fr/hal-02636033

Y. Nakajima, R. M. Goldblum, and T. Midoro-horiuti, Fetal exposure to bisphenol A as a risk factor for the development of childhood asthma: an animal model study, Environmental Health, vol.11, 2012.

E. O'brien, I. L. Bergin, D. C. Dolinoy, Z. Zaslona, R. J. Little et al., Perinatal bisphenol A exposure beginning before gestation enhances allergen sensitization, but not pulmonary inflammation, in adult mice, J Dev Orig Health Dis, vol.5, pp.121-131, 2014.

S. Omenetti, C. Bussi, A. Metidji, A. Iseppon, S. Lee et al., The Intestine Harbors Functionally Distinct Homeostatic Tissue-Resident and Inflammatory Th17 Cells, Immunity, vol.51, pp.77-89, 2019.

C. Park, H. Song, J. Choi, S. Sim, H. Kojima et al., The mixture effects of bisphenol derivatives on estrogen receptor and androgen receptor, Environ. Pollut, vol.260, 2020.

P. Pocar, B. Fischer, T. Klonisch, and S. Hombach-klonisch, Molecular interactions of the aryl hydrocarbon receptor and its biological and toxicological relevance for reproduction, Reproduction, vol.129, pp.379-389, 2005.

L. Prigent, M. Robineau, S. Jouneau, C. Morzadec, L. Louarn et al., The aryl hydrocarbon receptor is functionally upregulated early in the course of human T-cell activation, Eur. J. Immunol, vol.44, pp.1330-1340, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01063944

A. Rannug and U. Rannug, The tryptophan derivative 6-formylindolo[3,2-b]carbazole, FICZ, a dynamic mediator of endogenous aryl hydrocarbon receptor signaling, balances cell growth and differentiation, Crit. Rev. Toxicol, vol.48, pp.555-574, 2018.

L. R. Rhomberg and J. E. Goodman, Low-dose effects and nonmonotonic dose-responses of endocrine disrupting chemicals: Has the case been made?, Regulatory Toxicology and Pharmacology, vol.64, pp.130-133, 2012.

L. Robinson and R. Miller, The Impact of Bisphenol A and Phthalates on Allergy, Asthma, and Immune Function: a Review of Latest Findings, Curr Environ Health Rep, vol.2, pp.379-387, 2015.

J. R. Rochester, Bisphenol A and human health: A review of the literature, Reproductive Toxicology, vol.42, pp.132-155, 2013.

J. R. Rochester and A. L. Bolden, Bisphenol S and F: A Systematic Review and Comparison of the Hormonal Activity of Bisphenol A Substitutes, Environ. Health Perspect, vol.123, pp.643-650, 2015.

A. K. Rosenmai, M. Dybdahl, M. Pedersen, A. Van-vugt-lussenburg, B. M. Wedebye et al., Are structural analogues to bisphenol a safe alternatives?, Toxicol. Sci, vol.139, pp.35-47, 2014.

S. Savastano, G. Tarantino, V. D'esposito, F. Passaretti, S. Cabaro et al., Bisphenol-A plasma levels are related to inflammatory markers, visceral obesity and insulin-resistance: a cross-sectional study on adult male population, Journal of Translational Medicine, vol.13, 2015.

C. Schiering, A. Vonk, S. Das, B. Stockinger, and E. Wincent, Cytochrome P4501-inhibiting chemicals amplify aryl hydrocarbon receptor activation and IL-22 production in T helper 17 cells, Biochem. Pharmacol, vol.151, pp.47-58, 2018.

A. J. Spanier, R. S. Kahn, A. R. Kunselman, R. Hornung, Y. Xu et al., Prenatal Exposure to Bisphenol A and Child Wheeze from Birth to 3 Years of Age, Environmental Health Perspectives, vol.120, pp.916-920, 2012.

S. Tuomela, S. Rautio, H. Ahlfors, V. Öling, V. Salo et al., Comparative analysis of human and mouse transcriptomes of Th17 cell priming, Oncotarget, vol.7, pp.13416-13428, 2016.

S. V. Vaidya and H. Kulkarni, Association of Urinary Bisphenol A Concentration with Allergic Asthma: Results from the National Health and Nutrition Examination Survey, Journal of Asthma, vol.49, pp.800-806, 2005.

M. Van-voorhis, J. H. Fechner, X. Zhang, and J. D. Mezrich, The aryl hydrocarbon receptor: a novel target for immunomodulation in organ transplantation, Transplantation, vol.95, pp.983-990, 2013.

L. N. Vandenberg, P. A. Hunt, J. P. Myers, and F. S. Vom-saal, Human exposures to bisphenol A: mismatches between data and assumptions, Rev Environ Health, vol.28, pp.37-58, 2013.

M. Veldhoen, K. Hirota, J. Christensen, A. O'garra, and B. Stockinger, Natural agonists for aryl hydrocarbon receptor in culture medium are essential for optimal differentiation of Th17 T cells, J. Exp. Med, vol.206, pp.43-49, 2009.

H. Wu, B. Liu, K. Yang, G. N. Winston-mcpherson, E. D. Leisten et al., Synthesis and biological evaluation of FICZ analogues as agonists of aryl hydrocarbon receptor, Bioorganic & Medicinal Chemistry Letters, 2020.

E. Yamazaki, N. Yamashita, S. Taniyasu, J. Lam, P. K. Lam et al., Bisphenol A and other bisphenol analogues including BPS and BPF in surface water samples from Japan, China, Korea and India, Ecotoxicology and Environmental Safety, vol.122, pp.565-572, 2015.

O. Zenata, Z. Dvorak, and R. Vrzal, Profiling of bisphenol S towards nuclear receptors activities in human reporter cell lines, Toxicol. Lett, vol.281, pp.10-19, 2017.

L. Zhou, AHR Function in Lymphocytes: Emerging Concepts, Trends Immunol, vol.37, pp.17-31, 2016.

A. Ziv-gal, Z. R. Craig, W. Wang, and J. A. Flaws, Bisphenol A inhibits cultured mouse ovarian follicle growth partially via the aryl hydrocarbon receptor signaling pathway, Reprod. Toxicol, vol.42, pp.58-67, 2013.

, B) or from mouse siLP (C, D) were stimulated with anti-CD3 and anti-CD28 antibodies, and then pre-treated or not with CH-223191 before treatments with FICZ at 10 nM or TCDD at 10 nM for 4 days, p.22