The Effect of IFN-β Treatment on Plasma Levels of BDNF and IL-6 in Relapsing-Remitting Multiple Sclerosis Patients

被引:11
作者
Shajarian, Mansour [1 ]
Alsahebfosoul, Fereshteh [2 ]
Etemadifar, Masoud [3 ]
机构
[1] Isfahan Univ Med Sci, Appl Physiol Res Ctr, Cardiovasc Res Inst, Esfahan, Iran
[2] Isfahan Univ Med Sci, Sch Med, Dept Immunol, Esfahan, Iran
[3] Isfahan Univ Med Sci, Sch Med, Dept Neurol, Esfahan, Iran
关键词
Multiple sclerosis; Interleukin-6; Brain-derived neurotrophic factor; Interferon-beta treatment; Neurodegenerative diseases; NEUROTROPHIC FACTOR BDNF; NECROSIS-FACTOR-ALPHA; MESSENGER-RNA; SERUM-LEVELS; CEREBROSPINAL-FLUID; INTERLEUKIN-6; IL-6; HUMAN PLATELETS; TH17; CELLS; TNF-ALPHA; EXPRESSION;
D O I
10.1159/000515595
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In recent investigations addressing neurodegenerative diseases, especially multiple sclerosis (MS), the roles of brain-derived neurotrophic factor (BDNF) and interleukin-6 (IL-6) have been examined. Methods: Forty-five relapsing-remitting MS (RRMS) patients, including 32 IFN-beta-treated and 13 newly identified untreated cases as well as 45 sex- and age-matched healthy controls, were recruited in the study. Plasma levels of BDNF and IL-6 were assessed using the ELISA method. Data were analyzed by SPSS (ver.21). Results: There were significant differences between the case and healthy control groups in terms of the plasma levels of BDNF (p value = 0.044) and IL-6 (p value <0.001). Besides, the treatment with IFN-beta had no significant impact on the level of BDNF or IL-6 in RRMS patients as compared to healthy controls (p value = 0.716 and 0.623 for BDNF and IL-6, respectively). Furthermore, the increase in the plasma levels of BDNF and IL-6 indicated a direct correlation in the case group (r = 0.508, p value = 0.008). In detail, following the classification of the case group into 2 subgroups of IFN-beta-treated and untreated patients, a direct positive correlation was observed between the plasma levels of BDNF and IL-6 in IFN-beta-treated patients (r = 0.495, p value = 0.026). Conclusion: The IFN-beta treatment seems not to be effective for upregulating BDNF and IL-6 in RRMS patients.
引用
收藏
页码:150 / 157
页数:8
相关论文
共 53 条
[1]  
Alsahebfosoul Fereshteh, 2017, BioMolecular Concepts, V8, P55, DOI 10.1515/bmc-2016-0026
[2]   Lower brain-derived neurotrophic factor in serum of relapsing remitting MS: Reversal by glatiramer acetate [J].
Azoulay, D ;
Vachapova, V ;
Shihman, B ;
Miler, A ;
Karni, A .
JOURNAL OF NEUROIMMUNOLOGY, 2005, 167 (1-2) :215-218
[3]   Low and dysregulated BDNF secretion from immune cells of MS patients is related to reduced neuroprotection [J].
Azoulay, David ;
Urshansky, Natali ;
Karni, Arnon .
JOURNAL OF NEUROIMMUNOLOGY, 2008, 195 (1-2) :186-193
[4]   Interferon-β therapy up-regulates BDNF secretion from PBMCs of MS patients through a CD40-dependent mechanism [J].
Azoulay, David ;
Mausner-Fainberg, Karin ;
Urshansky, Nataly ;
Fahoum, Firas ;
Karni, Arnon .
JOURNAL OF NEUROIMMUNOLOGY, 2009, 211 (1-2) :114-119
[5]  
Bergman E, 1999, J COMP NEUROL, V410, P368, DOI 10.1002/(SICI)1096-9861(19990802)410:3<368::AID-CNE2>3.0.CO
[6]  
2-I
[7]   Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells [J].
Bettelli, E ;
Carrier, YJ ;
Gao, WD ;
Korn, T ;
Strom, TB ;
Oukka, M ;
Weiner, HL ;
Kuchroo, VK .
NATURE, 2006, 441 (7090) :235-238
[8]   Neurotrophic factors in relapsing remitting and secondary progressive multiple sclerosis patients during interferon beta therapy [J].
Caggiula, M ;
Batocchi, AP ;
Frisullo, G ;
Angelucci, F ;
Patanella, AK ;
Sancricca, C ;
Nociti, V ;
Tonali, PA ;
Mirabella, M .
CLINICAL IMMUNOLOGY, 2006, 118 (01) :77-82
[9]   Increased plasma levels of brain derived neurotrophic factor (BDNF) after multiple sclerosis relapse [J].
Comini Frota, Elizabeth Regina ;
Rodrigues, David Henrique ;
Donadi, Eduardo Antonio ;
Brum, Doralina G. ;
Kaimen Maciel, Damacio Ramon ;
Teixeira, Antonio Lucio .
NEUROSCIENCE LETTERS, 2009, 460 (02) :130-132
[10]   Vascular Cell Adhesion Molecule-1 Expression and Signaling During Disease: Regulation by Reactive Oxygen Species and Antioxidants [J].
Cook-Mills, Joan M. ;
Marchese, Michelle E. ;
Abdala-Valencia, Hiam .
ANTIOXIDANTS & REDOX SIGNALING, 2011, 15 (06) :1607-1638