Abstract
Background
Contact hypersensitivity (CHS) induced by a topical application of hapten - 2,4-dinitrofluorobenzene (DNFB), is a T cytotoxic (Tc)1-cell-mediated antigen-specific type of skin inflammation. Recently, it has been shown that antidepressant drugs inhibit the T helper (Th)1-mediated CHS reaction induced by picryl chloride. The aim of present study was to establish the effect of two-week desipramine or fluoxetine administration on the CHS reaction induced by DNFB.
Methods
Balb/c (H-2d) male mice were divided into six groups: 1) vehicle-treated negative control group; 2) desipramine-treated negative control group; 3) fluoxetine-treated negative control group; 4) vehicle-treated DNFB group (positive control group); 5) desipramine-treated DNFB group; 6) fluoxetine-treated DNFB group. T lymphocytes proliferation was determined by incorporation of [3H]-thymidine to DNA of concanavalin A stimulated cells. ELISA test was used for estimation of cytokines production.
Results
The antidepressants significantly suppressed the CHS reaction mediated by Tc1 cells: desipramine by 55% and fluoxetine by 54% compared to the positive control. Moreover, the antidepressants decreased the proliferative activity of splenocytes and the ability of splenocytes to produce interleukin (IL)-6 and interferon (IFN)-γ and increased IL-10 production by the lymph node (LN) cells of DNFB-treated mice.
Conclusion
The results of the present study show that the Tc1-dependent reactivity to DNFB is significantly suppressed by antidepressant drugs, which suggests their inhibitory effect on Tc1 mediated immunity.
Similar content being viewed by others
Change history
30 December 2017
The authors wish to note an incorrectly listed financial support grant. The National Science Centre grant 2011/01/B/NZ6/00300 was inadvertently listed. The authors regret this error. The correct Acknowledgements read as follows:
References
Askenase PW, Majewska-Szczepanik M, Kerfoot S, Szczepanik M: Participation of iNKT cells in the early and late components of Tc1-mediated DNFB contact sensitivity: cooperative role of 78-T cells. Scand J Immunol, 2011, 73, 465–477.
Askenase PW, Szczepanik M, Itakura A, Kiener C, Campos RA: Extravascular T-cell recruitment requires initiation begun by Vα14+ invariant NKT cells and B-1 B cells. Trends Immunol, 2004, 25, 441–449.
Barton BE, Shortall J, Jackson JV: Interleukins 6 and 11 protect mice from mortality in a staphylococcal enterotoxin-induced toxic shock model. Infect Immun, 1996, 64, 714–718.
Beer K, Albertini J, Medenica M, Busbey S: Fluoxetine-induced hypersensitivity. Arch Dermatol, 1994, 130, 803–804.
Boyman O, Wefel T, Akdis CA: The suppressive role of IL-10 in contact and atopic dermatitis. J Allergy Clin Immunol, 2012, 129, 160–161.
Dobrzanski MJ, Reome JB, Hylind JC, Rewers-Felkins KA: CD8-mediated type 1 antitumor responses selectively modulate endogenous differentiated and nondifferentiated T cell localization, activation, and function in progressive breast cancer. J Immunol, 2006, 177, 8191–8201.
Foussat A, Cottrez F, Brun V, Fournier N, Breittmayer JP, Groux H: A comparative study between T regulatory type 1 and CD4+CD25+ T cells in the control of inflammation. J Immunol, 2003, 171, 5018–5026.
Fujiwara R, Sasajima N, Takemura N, Ozawa K, Nagasaka Y, Okubo T, Sahasakul Y et al.: 2,4-Dinitrofluorobenzene-induced contact hypersensitivity response in NC/Nga mice fed fructo-oligosaccharide. J Nutr Sci Vitaminol (Tokyo), 2010, 56, 260–265.
Fyhrquist-Vanni N, Alenius H, Lauerma A: Contact dermatitis. Dermatol Clin, 2007, 25, 613–623.
Girard-Madoux MJH, Kel JM, Reizis B, Clausen BE: IL-10 controls dendritic cell-induced T-cell reactivation in the skin to limit contact hypersensitivity. J Allergy Clin Immunol, 2012, 129, 143–150.
Gorbachev AV, Fairchild RL: CD40 engagement enhances antigen-presenting Langerhans cell priming of IFN-γ-producing CD4+ and CD8+ T cells independently of IL-12. J Immunol, 2004, 173, 2443–2452.
Kubera M, Curzytek K, Majewska-Szczepanik M, Szczepanik M, Marcinska, Ptak W, Leśkiewicz M et al.: Inhibitory effect of antidepressant drugs on contact hypersensitivity reaction. Pharmacol Rep, 2012, 64, 714–722.
Kubera M, Grygier B, Arteta B, Urbańska K, Basta-Kaim A, Budziszewska B, Leśkiewicz M et al.: Age-dependent stimulatory effect of desipramine and fluoxetine pretreatment on metastasis formation by B16F10 melanoma in male C57BL/6 mice. Pharmacol Rep, 2009, 61, 1113–1126.
Kubera M, Holan V, Mathison R, Maes M: The effect of repeated amitriptyline and desipramine administration on cytokine release in C57BL/6 mice. Psychoneuroendocrinology, 2000, 25, 785–797.
Kubera M, Lin A-H, Kenis G, Bosmans E, van Bockstaele D, Maes M: Anti-inflammatory effects of antidepressants through suppression of the interferon-γ/interleukin-10 production ratio. J Clin Psychopharmacol, 2001, 21, 199–206.
Kubera M, Maes M, Budziszewska B, Basta-Kaim A, Leśkiewicz M, Grygier B, Rogóż Z, Lasoń W: Inhibitory effects of amantadine on the production of proinflammatory cytokines by stimulated in vitro human blood. Pharmacol Rep, 2009, 61, 1105–1112.
Kubera M, Maes M, Holan V, Basta-Kaim A, Roman A, Shani J: Prolonged desipramine treatment increases the production of interleukin-10, an anti-inflammatory cytokine, in C57BL/6 mice subjected to the chronic mild stress model of depression. J Affect Disord, 2001, 63, 171–178.
Kubera M, Simbirtsev A, Mathison R, Maes M: Effects of repeated fluoxetine and citalopram administration on cytokine release in C57BL/6 mice. Psychiatry Res, 2000, 96, 255–266.
Maes M, Song C, Lin AH, Bonaccorso S, Kenis G, de Jongh R, Bosmans E, Scharpé S: Negative immu-noregulatory effects of antidepressants: inhibition of interferon-yγ and stimulation of interleukin-10 secretion. Neuropsychopharmacology, 1999, 20, 370–379.
Pellegrino TC, Bayer BM: Modulation of immune cell function following fluoxetine administration in rats. Pharmacol Biochem Behav, 1998, 59, 151–157.
Riemann H, Schwarz A, Grabbe S, Aragane Y, Luger TA, Wysocka M, Kubin M et al: Neutralization of IL-12 in vivo prevents induction of contact hypersensitivity and induces hapten-specific tolerance. J Immunol, 1996, 156, 1799–1803.
Ring S, Schäfer SC, Mahnke K, Lehr HA, Enk AH: CD4+CD25+ regulatory T cells suppress contact hypersensitivity reactions by blocking influx of effector T cells into inflamed tissue. Eur J Immunol, 2006, 36, 2981–2992.
Sanz-Gallén P, Nogué S, Herrera-Mozo I, Delclos GL, Valero A: Occupational contact allergy to omeprazole and fluoxetine. Contact Dermatitis, 2011, 65, 118–119.
Schwarz A, Navid F, Sparwasser T, Clausen BE, Schwarz T: In vivo reprogramming of UV radiation-induced regulatory T-cell migration to inhibit the elicita-tion of contact hypersensitivity. J Allergy Clin Immunol, 2011, 128, 826–833.
Song C, Killeen AA, Leonard BE: Catalase, superoxide dismutase and glutathione peroxidase activity in neutrophils of sham-operated and olfactory-bulbectomised rats following chronic treatment with desipramine and lithium chloride. Neuropsychobiology, 1994, 30, 24–28.
Yuan XY, Ma HM, Li RZ, Wang RY, Liu W, Guo JY: Topical application of aloperine improves 2,4-dinitrofluorobenzene-induced atopic dermatitis-like skin lesions in NC/Nga mice. Eur J Pharmacol, 2011, 658, 263–269.
Zemelka-Wiącek M, Majewska-Szczepanik M, Ptak W, Szczepanik M: Epicutaneous immunization with protein antigen induces antigen-non-specific suppression of CD8 T cell mediated contact sensitivity. Pharmacol Rep, 2012, 64, 1485–1496.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Curzytek, K., Kubera, M., Majewska-Szczepanik, M. et al. Inhibition of 2,4-dinitrofluorobenzene-induced contact hypersensitivity reaction by antidepressant drugs. Pharmacol. Rep 65, 1237–1246 (2013). https://doi.org/10.1016/S1734-1140(13)71481-6
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1016/S1734-1140(13)71481-6