Guest guest Posted October 26, 2009 Report Share Posted October 26, 2009 Effects of interferon-beta therapy on innate and adaptive immune responses to the human endogenous retroviruses HERV-H and HERV-W, cytokine production, and the lectin complement activation pathway in multiple sclerosis Thor sena et al, Department of Neurology, Aarhus University Hospital, N©ªrrebrogade 44, DK-8000 Aarhus C, Denmark cImmunoendocrine Research Unit, Medical Department M (Diabetes and Endocrinology) and Medical Research Laboratories, Clinical Institute, Aarhus University Hospital, Aarhus, Denmark Received 6 July 2009; revised 26 August 2009; accepted 28 August 2009. Available online 18 September 2009. Abstract The effects of treatment of multiple sclerosis patients with IFN-¥â on elements in the innate and adaptive immune response were analysed in a longitudinal study. We demonstrate significant decreases in anti-Envelope antibody reactivity for the two closely related Gammaretroviral human endogenous retroviruses (HERVs), HERV-H and HERV-W, as a consequence of IFN-¥â therapy, closely linked to efficacy of therapy/low disease activity. We also show strong indications of a protective effect of high levels of two components in the innate pathogen-associated molecular pattern recognition: mannan-binding lectin (MBL), and MBL-associated serine protease 3 (MASP-3). Serum levels of typical Th1- and Th2-related, MS-relevant cytokines were also monitored. Overall both Th1- and Th2-associated cytokines were modestly, albeit significantly up-regulated, notably IL-2 and TNF-¥á (MS patients with inactive disease), as well as IL-4 and, to some extent IL-10 (no increase in IL-10 for MS patients with active disease (non-responders)). We found no overall changes in Th1/Th2 ratios. Our results support that HERV-H/HERV-W and the antiviral immune response may play a role in MS development, and that these HERVs have potential as biomarkers for disease activity. P.s. have full paper if anyone interested ------ End of Forwarded Message Quote Link to comment Share on other sites More sharing options...
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