In vivo effects of recombinant-interferon-beta(1b) treatment on polymorphonuclear cell and monocyte functions and on T-cell-mediated antibacterial activity in patients with relapsing-remitting multiple sclerosis
Ab. Maffione et al., In vivo effects of recombinant-interferon-beta(1b) treatment on polymorphonuclear cell and monocyte functions and on T-cell-mediated antibacterial activity in patients with relapsing-remitting multiple sclerosis, IMMUNOPH IM, 22(1), 2000, pp. 1-18
Treatment with Interferon (IFN)-beta has been proposed as a therapeutic app
roach in multiple sclerosis (MS) patients, mostly in view of its immunomodu
lating actions. At the same time, evidence has been provided that MS patien
ts exhibit polymorphonuclear cell (PMN) deficits, which can explain the inc
reased susceptibility to infections in these subjects. Here, in 28 patients
with relapsing-remitting (RR) MS under treatment with recombinant (r)-IFN-
beta PMN polarization and PMN and monocyte (MO) phagocytosis and killing, a
s well as T-cell mediated antibacterial activity, were evaluated before tre
atment and over a period of nine months of treatment.
Our results point out an enhanced rate of polarization (both "spontaneous"
or N-formyl-methionyl-leucyl-phenylalanine-induced) in MS patients. After r
-IFN-beta(1b) treatment the polarization rate was further increased. On the
contrary, PMN and MO phagocytosis and killing were depressed in comparison
to controls and values were further reduced by r-IFN-beta(1b) treatment.
In patients T-cell mediated antibacterial activity was decreased at T0 and
dramatically dropped in the course of r-IFN-beta(1b) therapy.