Treatment of depression is associated with suppression of nonspecific and antigen-specific T(H)1 responses in multiple sclerosis

Citation
Dc. Mohr et al., Treatment of depression is associated with suppression of nonspecific and antigen-specific T(H)1 responses in multiple sclerosis, ARCH NEUROL, 58(7), 2001, pp. 1081-1086
Citations number
55
Categorie Soggetti
Neurology,"Neurosciences & Behavoir
Journal title
ARCHIVES OF NEUROLOGY
ISSN journal
00039942 → ACNP
Volume
58
Issue
7
Year of publication
2001
Pages
1081 - 1086
Database
ISI
SICI code
0003-9942(200107)58:7<1081:TODIAW>2.0.ZU;2-I
Abstract
Objective: To examine the relationship between depression, treatment of dep ression, and interferon gamma (IFN-gamma) production by peripheral blood mo nonuclear cells in patients with comorbid diagnoses of relapsing-remitting multiple sclerosis (MS) and major depressive disorder. Design: A randomized comparative outcome trial of three 16-week treatments for depression. Assessments were conducted at baseline, week 8, and treatme nt cessation. Setting: An academic outpatient treatment and clinical research center. Patients: Fourteen patients who met the criteria for relapsing-remitting MS and major depressive disorder. Interventions: Individual cognitive behavioral therapy, group psychotherapy , or sertraline therapy. Main Outcome Measures: Depression was assessed using the Beck Depression In ventory. Interferon gamma production by peripheral blood mononuclear cells was measured following stimulation with OKT3 or recombinant human myelin ol igodendrocyte glycoprotein (MOG). Variability in immune assays was controll ed using 8 nondepressed healthy subjects who were enrolled at times corresp onding with the enrollment of MS patients. Results: Results of the Beck Depression Inventory were significantly relate d to IFN-gamma production stimulated with OKT3 or MOG at baseline (P less t han or equal to .03 for all). Level of depression, OKT3-stimulated IFN-gamm a production, and MOG-stimulated IFN-gamma production all declined signific antly over the 16-week treatment period (P less than or equal to .03 for al l). Among controls, there were no significant changes over time in OKT3-or MOG-stimulated IFN-gamma, or in depression (P greater than or equal to .25 for all). Conclusions: These findings suggest that the production of the proinflammat ory cytokine IFN-gamma by autoaggressive T cells in relapsing-remitting MS is related to depression and that treatment of depression may decrease IFN- gamma production. Thus, treatment of depression may provide a novel disease -modifying therapeutic strategy as well as a symptomatic treatment for pati ents with MS.