Multiple sclerosis (MS) is a T-cell-mediated autoimmune demyelinating
disease of the central nervous system (CNS), associated with an altere
d immunoregulation. Interferon (IFN)-gamma, also known as immune IFN,
is a cytokine with several effects on the immune system. Specific IFN-
gamma receptors have been found on human lymphocytes, as well as on ot
her cell types (e.g. gliocytes), even in the CNS. The aim of the prese
nt study was to evaluate IFN-gamma binding on peripheral blood T-lymph
ocytes from MS patients, compared with those from healthy subjects. Th
irty-two patients were selected according to the classical criteria fo
r definite MS; as controls, 21 healthy subjects were studied. We have
found that T-lymphocytes from MS patients bear a significantly smaller
amount of IFN-gamma receptors than those from controls [B-max: 568, 1
8 vs 708, 14 (mean, SE) receptors/cell]. Such TFN-gamma binding sites
are of the same type in patients and healthy subjects [K-d: 1.0, 0.05
vs 0.9, 0.02 (mean, SE) nM]. These findings are discussed in terms of
immunopathogenesis of MS, since it has been reported that activated T-
lymphocytes have decreased amounts of IFN-gamma receptors.