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Article type: Research Article
Authors: Taheri, Mohammada | Nemati, Shirina | Movafagh, Abolfazla | Saberi, Mohammadb | Mirfakhraie, Rezaa | Eftekharian, Mohammad Mahdic; d | Arsang-Jang, Shahrame | Rezagholizadeh, Amira | Sayad, Arezoua; *
Affiliations: [a] Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran | [b] Department of Medical Genetics, Tehran medical University of Medical Sciences, Tehran, Iran | [c] Neurophysiology Research Center, Hamadan University of Medical Sciences and Health Services, Hamadan, Iran | [d] Molecular Immunology Research Group, Hamadan University of Medical Sciences and Health Services, Hamadan, Iran | [e] Department of Epidemiology and Biostatistics, Faculty of Health, Qom University of Medical Sciences, Qom, Iran
Correspondence: [*] Corresponding author: Arezou Sayad, Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, PO Box 1985717443, Tehran, Iran. Tel.: +98 21 23872572; Fax: +98 2123872572; E-mail:ar.sayad@sbmu.ac.ir
Abstract: BACKGROUND: Multiple sclerosis (MS) as an autoimmune disorder in which the insulating covers of neurons in the Central Nervous System are destructed. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is an immunomodulatory molecule to protect against T cells hyper activation. METHODS: In this Case-control study, we compare TRAIL gene expression in peripheral blood between 50 relapse remitting MS patients and 50 healthy controls by TaqMan Real time PCR. All the patients were negative for HLA-DRB1*15 susceptible allele, normal serum vitamin D, responder to Interferon beta. All the health individuals were matched to patients. Also, we tried to find correlation between TRAIL gene expression and clinical characteristics of patients. RESULTS: No statistically significant difference was found in TRAIL mRNA expression between MS patients and controls (p> 0.05). There was no correlation in the TRAIL expression and age of onset, disease duration and Expanded Disability Status Scale of Kurtzke (EDSS). As IFN-b may have stimulatory effects on immunoregulatory function of TRAIL and all of our patients were treated with interferon beta and were responder, it lead to no significant change in TRAIL expression. We suggest comparing between responders and non-responders should be investigated.
Keywords: TRAIL, multiple sclerosis, gene expression
DOI: 10.3233/HAB-160291
Journal: Human Antibodies, vol. 24, no. 1-2, pp. 33-38, 2016
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