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      CCR5Δ32 Polymorphism Associated with a Slower Rate Disease Progression in a Cohort of RR-MS Sicilian Patients

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          Abstract

          Multiple sclerosis (MS) disease is carried through inflammatory and degenerative stages. Based on clinical feaures, it can be subdivided into three groups: relapsing-remitting MS, secondary progressive MS, and primary progressive MS. Multiple sclerosis has a multifactorial etiology with an interplay of genetic predisposition, environmental factors, and autoimmune inflammatory mechanism in which play a key role CC-chemokines and its receptors. In this paper, we studied the frequency of CCR5 gene Δ32 allele in a cohort of Sicilian RR-MS patients comparing with general Sicilian population. Also, we evaluate the association between this commonly polymorphism and disability development and age of disease onset in the same cohort. Our results show that presence of CCR5Δ32 is significantly associated with expanded disability status scale score (EDSS) but not with age of disease onset.

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          Most cited references42

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          Molecular Cloning : A Laboratory Manual

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            Chemokines and disease.

            We examine here several diseases that are associated with inappropriate activation of the chemokine network. Detailed comment has been restricted to pathological states for which there are compelling data either from clinical observations or animal models. These include cardiovascular disease, allergic inflammatory disease, transplantation, neuroinflammation, cancer and HIV-associated disease. Discussion focuses on therapeutic directions in which the rapidly evolving chemokine field appears to be headed.
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              Cytokines in multiple sclerosis: from bench to bedside.

              Cytokines play an important role in the pathogenesis of inflammatory diseases including multiple sclerosis (MS). Experimental models have played a critical role in unraveling the roles of individual cytokines in this disease; however, these studies occasionally yield conflicting results, highlighting the complex role cytokines play in the disease process. Efforts to modulate cytokine function in MS have shown that effective treatments alter cytokine expression in the central nervous system (CNS) and in activated mononuclear cells, indicating that they are important therapeutic targets. In this review, we will summarize the current knowledge on the role of cytokine pathways in MS and what we learned from investigation of its animal model: experimental autoimmune encephalomyelitis (EAE).
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                Author and article information

                Journal
                Mult Scler Int
                MSI
                Multiple Sclerosis International
                Hindawi Publishing Corporation
                2090-2654
                2090-2662
                2011
                23 June 2011
                : 2011
                : 153282
                Affiliations
                Department of Biomorphology and Biotechnologies, University of Messina, 98125 Messina, Italy
                Author notes
                *Concetta Crisafulli: ccrisafulli@ 123456unime.it

                Academic Editor: Oscar Fernandez

                Article
                10.1155/2011/153282
                3195283
                22096627
                35722c0b-7235-4228-a8b1-3da780497aab
                Copyright © 2011 Rosalia D'Angelo et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 15 November 2010
                : 19 February 2011
                Categories
                Research Article

                Rheumatology
                Rheumatology

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