The cellular response to endoplasmic reticulum (ER) stress accompanies plasma cell maturation and is one of triggers and cofactors of the local inflammatory response. Chemical chaperones, low-molecular substances that eliminate pathological ER stress, are proposed as means of treating pathologies associated with ER stress. The aim of this study was to evaluate the effect and mechanisms of influence of chemical chaperones on the humoral response in a low-dose model of allergy. The allergic immune response was induced in BALB/c mice by repeated administration of ovalbumin at a dose of 100 ng for 6 weeks. Some animals were injected with both the antigen and the chemical chaperones, TUDCA (tauroursodeoxycholic acid) or 4-PBA (4-phenylbutyrate). Administration of TUDCA, but not 4-PBA, suppressed production of allergen-specific IgE (a 2.5-fold decrease in titer). None of the chemical chaperones affected the production of specific IgG₁. The effect of TUDCA was associated with suppression of the switch to IgE synthesis in regional lymph nodes. This phenomenon was associated with suppressed expression of genes encoding cytokines involved in type 2 immune response, especially Il4 and Il9, which in turn could be caused by suppression of IL-33 release. In addition, TUDCA significantly suppressed expression of the cytokine APRIL, and to a lesser extent, BAFF. Thus, TUDCA inhibition of the allergy-specific IgE production is due to suppression of the release of IL-33 and a decrease in the production of type 2 immune response cytokines, as well as suppression of the expression of the cytokines APRIL and BAFF.
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Keywords: chemical chaperone, taurodeoxycholate, IgE, interleukin 4, interleukin 33, APRIL, BAFF
Citation:
Chudakov D.B., Shustova O.A., Kotsareva O.D., Generalov A.A., Streltsova M.S., Vavilova Yu.D., Fattakhova G.V. (2024) Chemical chaperone TUDCA selectively inhibits production of allergen-specific IgE in a low-dose model of allergy. Biomeditsinskaya Khimiya, 70(1), 5-14.
Chudakov D.B. et al. Chemical chaperone TUDCA selectively inhibits production of allergen-specific IgE in a low-dose model of allergy // Biomeditsinskaya Khimiya. - 2024. - V. 70. -N 1. - P. 5-14.
Chudakov D.B. et al., "Chemical chaperone TUDCA selectively inhibits production of allergen-specific IgE in a low-dose model of allergy." Biomeditsinskaya Khimiya 70.1 (2024): 5-14.
Chudakov, D. B., Shustova, O. A., Kotsareva, O. D., Generalov, A. A., Streltsova, M. S., Vavilova, Yu. D., Fattakhova, G. V. (2024). Chemical chaperone TUDCA selectively inhibits production of allergen-specific IgE in a low-dose model of allergy. Biomeditsinskaya Khimiya, 70(1), 5-14.
References
Hellman L. (2007) Regulation of IgE homeostasis, and the identification of potential targets for therapeutic intervention. Biomed. Pharmacother., 61(1), 34-49. CrossRef Scholar google search
Gass J.N., Gunn K.E., Sriburi R., Brewer J.W. (2004) Stressed-out B cells? Plasma-cell differentiation and the unfolded protein response. Trends Immunol., 25(11), 17-24. CrossRef Scholar google search
Mesitov M.V., Moskovcev A.A., Kubatiev A.A. (2013) Molecular logic of signaling pathways during endoplasmic reticulum stress: the UPR (Unfolded Protein Response) system. Pathological physiology and experimental therapy. Patologicheskaya Fiziologiya i Eksperimental'naya Terapiya, 57(4), 97-108. Scholar google search
Ma Y., Shimizu Y., Mann M.J., Hendershot L.M. (2010) Plasma cell differentiation initiates a limited ER stress response by specifically suppressing the PERK-dependent branch of the unfolded protein response. Cell Stress Chaperones, 15(3), 281-293. CrossRef Scholar google search
Liu J.-X., Zhen Z., Chen A.-N., Guo C.-L., Shi K.-T., Wang H., Xu K., Yao Y., Wang H., Liao B., Liu Z. (2021) Endoplasmic reticulum stress promotes local immunoglobulin E production in allergic rhinitis. Laryngoscope Investig. Otolaryngol., 6(6), 1256-1266. CrossRef Scholar google search
Kim S., Joe Y., Surh Y.-J., Chung H.T. (2018) Differential regulation of toll-like receptor-mediated cytokine production by unfolded protein response. Oxid. Med. Cell Longev., 2018, 9827312. CrossRef Scholar google search
Kemp K.L., Lin Z., Zhao F., Gao B., Song J., Zhang K., Fang D. (2013) The serine-threonine kinase inositol-requiring enzyme 1α (IRE1α) promotes IL-4 production in T helper cells. J. Biol. Chem., 288(46), 33272-33282. CrossRef Scholar google search
Cortez L., Sim V. (2014) The therapeutic potential of chemical chaperones in protein folding diseases. Prion, 8(2), 197-202. CrossRef Scholar google search
Mihajlova V.V., Eronina T.B., Chebotareva N.A., Kurganov B.I. (2023) The influence of chemical chaperones on protein aggregation processes occurring in various kinetic regimes. Biochemistry (Moscow), 88(1), 83-96. CrossRef Scholar google search
Chudakov D.B., Kotsareva O.D., Konovalova M.V., Tsaregorotseva D.S., Schevchenko M.A., Sergeev A.A., Fattakhova G.V. (2022) Early IgE production is linked with extrafollicular B- and T-cell activation in low-dose allergy model. Vaccines, 10(6), 969. CrossRef Scholar google search
Chudakov D.B., Ryasantsev D.Yu., Tsaregorotseva D.S., Kotsareva O.D., Fattakhova G.V., Svirshchevskaya E.V. (2020) Tertiary lymphoid structure related B-cell IgE isotype switching and secondary lymphoid organ linked IgE production in mouse allergy model. BMC Immunology, 21(1), 45. CrossRef Scholar google search
Xu Z., Zan H., Pone E.J., Mai T., Casali P. (2012) Immunoglobulin class-switch DNA recombination: Induction, targeting and beyond. Nat. Rev. Immunol., 12(7), 517-531. CrossRef Scholar google search
Labmrecht B.N., Hammad H. (2014) Allergens and the airway epithelium response: Gateway to allergic sensitization. J. Allergy Clin. Immunol., 134(3), 499-507. CrossRef Scholar google search
Chan B.C.L., Lam C.W.K., Tam L.-S., Wong C.K. (2019) IL33: Roles in allergic inflammation and therapeutic perspectives. Front. Immunol., 10, 364. CrossRef Scholar google search
Nakada E.M., Bhakta N.R., Korwin-Michavics B.R., Kumar A., Chamberlain N., Bruno S.R., Chapman D.G., Hoffman S.M., Daphtary N., Aliyeva M., Irvin C.G., Dixon A.E., Woodruff P.G., Amin S., Poynter M.E., Desai D.H., Anathy V. (2019) Conjugated bile acids attenuate allergen-induced airway inflammation and hyperresponsiveness by inhibiting UPR transducers. JCI Insight., 4(9), E98101. CrossRef Scholar google search
Siddesha J.M., Nakada E.M., Michavicks B.R., Hoffman S.M., Rattu G.K., Chamberlain N., Cahoon J.M., Lahue K.G., Daphtary N., Aliyeva M., Chapman D.G., Desai D.H., Poynter M.E., Anathy V. (2016) Effect of a chemical chaperone, tauroursodeoxycholic acid, on HDM-induced allergic airway disease. Am. J. Physiol. Lung Cell Mol. Physiol., 310(11), 1243-1259. CrossRef Scholar google search
Uppala J.K., Gani A.R., Ramaiah K.V.A. (2017) Chemical chaperone, TUDCA unlike PBA, mitigates protein aggregation efficiently and resists ER and non-ER stress induced HepG2 cell death. Sci. Rep., 7(1), 3831. CrossRef Scholar google search
Tsukamoto Y., Uehara S., Mizoguchi C., Sato A., Horikawa K., Takatsu K. (2005) Requirement of 8-mercaptoguanosine as a costimulus for IL-4-dependent μ to γ1 class switch recombination in CD38-activated B cells. Biochem. Biophys. Res. Commun., 336, 625-633. CrossRef Scholar google search
Wang Y., Shi J., Yan J., Xiao Z., Hou X., Lu P., Hou S., Mao T., Liu W., Ma Y., Zhang L., Yang X., Qi H. (2017) Germinal-center development of memory B cells driven by IL-9 from follicular helper T cells. Nat. Immunol., 18(8), 921-930. CrossRef Scholar google search
Turner J.-E., Morrison P.J., Wilhelm C., Wislon M., Ahifors H., Renauld J.-C., Panzer U., Helmby H., Stockinger B. (2013) IL-9-mediated survival of type 2 innate lymphoid cells promotes damage control in helminth-induced lung inflammation. J. Exp. Med., 210(13), 2951-2965. CrossRef Scholar google search
Meli A.P., Fontes G., Soo C.L., King I.L. (2017) T follicular helper cell-derived IL-4 is required for IgE production during intestinal helminth infection. J. Immunol., 199(1), 244-252. CrossRef Scholar google search
Khaitov M.R., Gaisina A.R., Shilovskiy I.P., Smirnov V.V., Ramenskaia G.V., Nikonova A.A., Khaitov R.M. (2018) The role of interleukin-33 in pathogenesis of bronchial asthma. New experimental data. Biochemistry (Moscow), 83(1), 13-25. CrossRef Scholar google search
Zan H., Casali P. (2013) Regulation of Aicda expression and AID activity. Autoimmunity, 46(2), 86-101. CrossRef Scholar google search
Castigli E., Wilson S., Scott S., Dedeoglu F., Xu S., Lam K.-P., Bram R., Jabara H., Geha R. (2005) TACI and BAFF-R mediate isotype switching in B cells. J. Exp. Med., 201(1), 35-39. CrossRef Scholar google search
Janssen E., Ozcan E., Liadaki K., Jabara H.H., Manis J., Ullas S., Akira S., Fitzgerald K.A., Golenbock D.T., Geha R.S. (2014) TRIF signaling is essential for TLR4-driven IgE class switching. J. Immunol., 192(6), 2651-2658. CrossRef Scholar google search
Dilidaer T., Zheng Y., Liu Z., Hu X., Zhang J., Hu L., Han M., Wang D., Li H. (2017) Increased BAFF expression in nasal polyps is associated with local IgE production, Th2 response and concomitant asthma. Eur. Arch. Otorhinolaryngol., 274(4), 1883-1890. CrossRef Scholar google search
Matsushita T., Fujimoto M., Echigo T., Matsushita Y., Shimada Y., Hasegawa M., Takehara K., Sato S. (2008) Elevated serum levels of APRIL, but not BAFF, in patients with atopic dermatitis. Exp. Dermatol., 17(3), 197-202. CrossRef Scholar google search