Combined treatment with desloratadine (histamine H1-receptor antagonist) and nortriptyline (tricyclic-antidepressant [TCA]) |
Mice with relapsing-remitting EAE |
The combined in vivo treatment with deloratadine (3 mg/kg) and Nortriptyline (10 mg/kg) decreases the IL-17 production by PLP or anti-CD3-activated splenocytes and anti-CD3-activated lymph node cells in mice with EAE. Nortriptyline (0–1mM) dose-dependently reduced IL-17 production by PLP and OVA activated lymph node cells and anti-CD3/anti-CD28-activated naive CD4+ T-cells. |
Podojil et al., 2011 (67) |
Desipramine (TCA) |
Mice with allergic rhinitis (AR) and depression |
Desipramine administration (3 mg/kg, 10 mg/kg or 30 mg/kg) decreased CD4+IL-17+/CD4+ T-cells ratio in AR mice spleen cells. |
Zhang et al., 2013 (68) |
Amitriptyline (TCA) |
Mice with C. rodentium infection |
Treatment with amitriptyline (180 mg/l via drinking water for 14 days before infection and 10 days during infection) enhance frequencies of CD4+IL-17+ and CD4+IFN-γ+ T-cells cells through acid sphingomyelinase inhibition. |
Meiners et al., 2019 (69) |
Paroxetine (selective serotonin reuptake inhibitor [SSRI]) |
Rats with collagen-induced arthritis (CIA) |
The in vitro treatment of murine CD3+ T-cells with paroxetine (10–5 M) prevents Th17-cells differentiation under IL-6/TGF-β/IL-23 induction via GRK2 inhibition. The in vivo treatment of CIA rats with paroxetine (15 mg/kg/day) significantly reduced the splenic Th17-cells. |
Hu et al., 2021 (70) |
Fluoxetine (SSRI) |
RRMS with depression |
The treatment with fluoxetine (20 mg/day) during 6 months reduced the IL-17 production by Pam3C or LPS-activated CD4+ and CD8+ T-cells. |
Sales et al., 2021 (49) |
Fluoxetine |
RRMS |
Fluoxetine (10–6 M) suppresses IL-17, IFN-γ, and GM-CSF production by anti-CD3/CD28-activated CD4+ T-cells in RRMS patients and healthy subjects. 5-HT2B-receptor antagonist reduced the inhibitory effect of fluoxetine on cytokine production in MS patients. |
Sviridova et al., 2021 (18) |