| dc.contributor.author | Hasheminia, Seyed Javad | en_US |
| dc.contributor.author | Zarkesh-Esfahani, Sayyed Hamid | en_US |
| dc.contributor.author | Tolouei, Sepideh | en_US |
| dc.contributor.author | Shaygannejad, Vahid | en_US |
| dc.contributor.author | Shirzad, Hedaiatallah | en_US |
| dc.contributor.author | Hashemzadeh Chaleshtory, Morteza | en_US |
| dc.date.accessioned | 1399-07-09T07:48:32Z | fa_IR |
| dc.date.accessioned | 2020-09-30T07:48:32Z | |
| dc.date.available | 1399-07-09T07:48:32Z | fa_IR |
| dc.date.available | 2020-09-30T07:48:32Z | |
| dc.date.issued | 2014-06-01 | en_US |
| dc.date.issued | 1393-03-11 | fa_IR |
| dc.date.submitted | 2016-08-04 | en_US |
| dc.date.submitted | 1395-05-14 | fa_IR |
| dc.identifier.citation | Hasheminia, Seyed Javad, Zarkesh-Esfahani, Sayyed Hamid, Tolouei, Sepideh, Shaygannejad, Vahid, Shirzad, Hedaiatallah, Hashemzadeh Chaleshtory, Morteza. (2014). Toll Like Receptor 2 and 4 Expression in Peripheral Blood Mononuclear Cells of Multiple Sclerosis Patients. Iranian Journal of Immunology, 11(2), 74-83. | en_US |
| dc.identifier.issn | 1735-1383 | |
| dc.identifier.issn | 1735-367X | |
| dc.identifier.uri | https://iji.sums.ac.ir/article_16768.html | |
| dc.identifier.uri | https://iranjournals.nlai.ir/handle/123456789/329296 | |
| dc.description.abstract | <b>Background</b>: <span lang="JA">Multiple sclerosis (MS) is a T cell mediated autoimmune disease with</span> unknown etiology. Appropriate MS therapeutic strategies need thorough understanding of both disease etiology and pathogenesis mechanisms. Ligation of TLR-2 and TLR-4 stimulates the production of several cytokines leading to CNS autoimmunity and neurodegenerative diseases. <span><br/><b>Objective</b>: </span><span lang="JA">To find a relationship between MS disability</span> and TLR-2 and TLR-4 expression on mononuclear cells in the blood of MS patients. <br/><b>Methods</b>: <span lang="JA">Forty-five new case (NC) MS patients (33 females and 12 males) and 45 age</span> and gender-matched healthy controls (HC) were recruited to the study. PBMCs were prepared and the expressions of TLR-2 and TLR-4 were assessed by flowcytometry technique using appropriate monoclonal antibodies. <span><br/><b>Results</b>: </span><span lang="JA">Our results showed that</span> the expression of TLR-2 and TLR-4 proteins in the patients group was significantly higher than that of healthy controls. TLR-2 but not TLR-4 was correlated with expanded disability status scale (EDSS) scores. <span><br/><b>Conclusion</b>: </span><span lang="JA">High expressions of TLR-2 and</span> TLR-4 may represent a state of innate immune activation in patients with MS. | en_US |
| dc.language | English | |
| dc.language.iso | en_US | |
| dc.publisher | Shiraz Institute for Cancer Research | en_US |
| dc.relation.ispartof | Iranian Journal of Immunology | en_US |
| dc.subject | Multiple Sclerosis | en_US |
| dc.subject | TLR-2 | en_US |
| dc.subject | TLR-4 | en_US |
| dc.subject | PBMC | en_US |
| dc.title | Toll Like Receptor 2 and 4 Expression in Peripheral Blood Mononuclear Cells of Multiple Sclerosis Patients | en_US |
| dc.type | Text | en_US |
| dc.type | Original Article | en_US |
| dc.contributor.department | Cellular and Molecular Research Center, School of Medicine, Shahre Kord University of Medical
Sciences, Shahre Kord | en_US |
| dc.contributor.department | Department of Biology, School of Sciences, University of Isfahan | en_US |
| dc.contributor.department | Department of
Parasitology and Mycology, School of Medicine, Isfahan University of Medical Sciences | en_US |
| dc.contributor.department | Department of
Neurology, School of Medicine, Isfahan University of Medical Sciences, Isfahan | en_US |
| dc.contributor.department | Department of
Immunology, School of Medicine, Shahre Kord University of Medical Sciences | en_US |
| dc.contributor.department | Cellular and Molecular
Research Center, School of Medicine, Shahre Kord University of Medical Sciences, Shahre Kord , Iran | en_US |
| dc.citation.volume | 11 | |
| dc.citation.issue | 2 | |
| dc.citation.spage | 74 | |
| dc.citation.epage | 83 | |