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Multiple sclerosis-associated retroviral agent (MSRV)-stimulated cytokine production in patients with relapsing-remitting multiple sclerosisLaboratory of Molecular Medicine and Biotechnology, Don C. Gnocchi ONLUS Foundation IRCCS, Via Capecelatro, 66, Milano 20148, Italy
Laboratoire dImmunochimie,CEA/INSERUM-U548, 17 rue des Martyrs 38054 Grenoble, France
Laboratory of Molecular Medicine and Biotechnology, Don C. Gnocchi ONLUS Foundation IRCCS, Via Capecelatro, 66, Milano 20148, Italy
Multiple Sclerosis Unit, Don C. Gnocchi ONLUS Foundation, IRCCS, Via Capecelatro, 66, Milano 20148, Italy
Multiple Sclerosis Unit, Don C. Gnocchi ONLUS Foundation, IRCCS, Via Capecelatro, 66, Milano 20148, Italy
Laboratoire dImmunochimie,CEA/INSERUM-U548, 17 rue des Martyrs 38054 Grenoble, France
GeNeuro, Geneva; 1228 Plan-Lesouates, Switzerland
Laboratory of Molecular Medicine and Biotechnology, Don C. Gnocchi ONLUS Foundation IRCCS, Via Capecelatro, 66, Milano 20148, Italy; Chair of Immunology, Department of Biomedical Sciences and Technologies, University of Milano, Via Fratelli Cervi 93, Milano 20090, Italy mario.clerici{at}unimi.it Background Human endogenous retroviruses are suggested to play a pathogenic role in multiple sclerosis (MS); one of such retroviruses, the MS-associated retroviral agent (MSRV) has repeatedly been isolated in MS patients. Objective and methods
We analyzed cytokine profiles in MSRV envelope protein (MSRV ENV-SU)-stimulated peripheral blood mononuclear cells of 30 relapsing-remitting MS patients with either acute (AMS) (n = 13) or stable (SMS) (n = 17) disease. Results suggest that MSRV ENV-SU induces the production of inflammatory cytokines, including tumor necrosis factor- Conclusions These data strengthen the hypothesis indicating that MSRV could be involved in the pathogenesis of MS.
Key Words: cytokines ENV-SU protein human endogenous retroviruses (HERV) immunology multiple sclerosis T lymphocytes
This version was published on April
1, 2009 Multiple Sclerosis, Vol. 15, No. 4,
443-447 (2009) |
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(P < 0.05) and interferon-
(P < 0.004) in AMS patients and of interleukin-10 (P < 0.05), an inflammation-dampening cytokine, in SMS individuals.