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
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.