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dc.contributor.advisorBaradaran, Behzad
dc.contributor.advisorHajialilo, Mehrzad
dc.contributor.authorShomali, Navid
dc.date.accessioned2022-11-07T06:28:30Z
dc.date.available2022-11-07T06:28:30Z
dc.date.issued2022en_US
dc.identifier.urihttps://dspace.tbzmed.ac.ir:443/xmlui/handle/123456789/67619
dc.description.abstractAnkylosing spondylitis (AS) is progressive immune-mediated arthritis. Persistent autoreactivity of T cells with an up-regulated Survivin expression is strongly implicated in AS immunopathogenesis. Material and methods: PBMCs were isolated from patients with AS and healthy matched controls using Ficoll-Hypaque. T cells were obtained using the magnetic-activated cell sorting (MACS) method. After that, the expression levels of Survivin, and specific miRNAs were determined using qT-qPCR. Then, the isolated T cells were co-cultured with interleukin (IL)-2 and muromonab-CD3 (OKT-3 to assess the correlation between T lymphocytes' resistance to apoptosis by determining the rate of apoptosis by Flowcytometry assay. Results: The results showed that Survivin was up-regulated in patients with AS. It was also revealed that microRNAs that directly or indirectly target the Survivin mRNA were dysregulated in patients with AS. It was revealed that T cells obtained from AS patients were more resistant to apoptosis induction than those obtained from healthy people.en_US
dc.language.isofaen_US
dc.publisherTabriz University of Medical Sciences, Faculty of Medicineen_US
dc.relation.isversionofhttps://dspace.tbzmed.ac.ir:443/xmlui/handle/123456789/67618en_US
dc.subjectAnkylosing spondylitisen_US
dc.subjectSurvivinen_US
dc.subjectmiRNAen_US
dc.subjectT cellsen_US
dc.subjectApoptosisen_US
dc.titleDetermination of Survivin expression in patients with Ankylosing Spondylitis and its relation with the survival of autoreactive T lymphocytes and microRNAs related to this pathway following stimulation to enter the activation-induced cell death phase (AICD)en_US
dc.typeThesisen_US
dc.contributor.supervisorSandoghchian Shotorbani, Siamak
dc.identifier.docno6010624en_US
dc.identifier.callno10624en_US
dc.description.disciplineImmunologyen_US
dc.description.degreePh. Den_US


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