RORγT is overexpressed in iNKT and γδ T cells during relapse in relapsing-remitting multiple sclerosis

被引:6
作者
Zarobkiewicz, Michal K. [1 ]
Kowalska, Wioleta [1 ]
Halczuk, Pawel [2 ,3 ,4 ]
Wos, Justyna [1 ]
Jodlowska-Jedrych, Barbara [3 ,4 ]
Rejdak, Konrad [2 ]
Rolinski, Jacek [1 ]
Bojarska-Junak, Agnieszka A. [1 ]
机构
[1] Med Univ Lublin, Dept Clin Immunol, Chodzki 4a St, PL-20093 Lublin, Poland
[2] Med Univ Lublin, Dept Neurol, Lublin, Poland
[3] Med Univ Lublin, Dept Histol, Lublin, Poland
[4] Med Univ Lublin, Embryol Expt Cytol Unit, Lublin, Poland
关键词
gamma delta T; IL-17; iNKT; Th17; Multiple sclerosis; ROR gamma T; NATURAL-KILLER T; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; CENTRAL-NERVOUS-SYSTEM; CEREBROSPINAL-FLUID; PERIPHERAL-BLOOD; TRANSCRIPTION FACTORS; IL-17; PRODUCTION; GENE-EXPRESSION; NKT CELLS; INFLAMMATION;
D O I
10.1016/j.jneuroim.2019.577046
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The aim of the current study is to evaluate IL-17 production and ROR gamma T, and IL-23R expression by iNKT, Th17 and gamma delta T cells in the peripheral blood of relapsing-remitting multiple sclerosis patients. Samples of peripheral blood from 21 relapse patients and 12 remission patients, and 15 healthy volunteers were stained with monoclonal antibodies for flow cytometry analysis. No significant differences in iNKT, gamma delta T and Th17 percentages were noted. The significant overexpression of ROR gamma T was observed in all three subpopulations - therefore, iNKT, gamma delta T and Th cells may be an important source of IL-17 shortly prior to the relapse.
引用
收藏
页数:9
相关论文
共 31 条
[1]   User's guide to correlation coefficients [J].
Akoglu, Haldun .
TURKISH JOURNAL OF EMERGENCY MEDICINE, 2018, 18 (03) :91-93
[2]   Th2 bias of CD4+ NKT cells derived from multiple sclerosis in remission [J].
Araki, M ;
Kondo, T ;
Gumperz, JE ;
Brenner, MB ;
Miyake, S ;
Yamamura, T .
INTERNATIONAL IMMUNOLOGY, 2003, 15 (02) :279-288
[3]   An improved flow cytometric method using FACS lysing solution for measurement of ZAP-70 expression in B-cell chronic lymphocytic leukemia [J].
Bekkema, Roelof ;
Tadema, Afke ;
Daenen, Simon M. G. J. ;
Kluin-Nelemans, Hanneke C. ;
Mulder, Andre B. .
CYTOMETRY PART B-CLINICAL CYTOMETRY, 2008, 74B (01) :40-44
[4]  
Chan Y H, 2003, Singapore Med J, V44, P614
[5]   Transcription Factors and Th17 Cell Development in Experimental Autoimmune Encephalomyelitis [J].
Chen, Guobing ;
Shannon, M. Frances .
CRITICAL REVIEWS IN IMMUNOLOGY, 2013, 33 (02) :165-182
[6]   Adoptively transferred EAE in γδ T cell-knockout mice [J].
Clark, RB ;
Lingenheld, EG .
JOURNAL OF AUTOIMMUNITY, 1998, 11 (01) :105-110
[7]   A biased Vα24+ T-cell repertoire leads to circulating NKT-cell defects in a multiple sclerosis patient at the onset of his disease [J].
Démoulins, T ;
Gachelin, G ;
Bequet, D ;
Dormont, D .
IMMUNOLOGY LETTERS, 2003, 90 (2-3) :223-228
[8]   Altered Expression of Specific Transcription Factors of Th17 (RORγt, RORα) and Treg Lymphocytes (FOXP3) by Peripheral Blood Mononuclear Cells from Patients with Multiple Sclerosis [J].
Etesam, Zahra ;
Nemati, Maryam ;
Ebrahimizadeh, Mohammad-Amin ;
Ebrahimi, Hossain-Ali ;
Hajghani, Hossain ;
Khalili, Tahereh ;
Frootan, Razieyeh ;
Zinoddini, Nahid ;
Jafarzadeh, Abdollah .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2016, 60 (01) :94-101
[9]   Innate immunity modulates autoimmunity:: type 1 interferon-β treatment in multiple sclerosis promotes growth and function of regulatory invariant natural killer T cells through dendritic cell maturation [J].
Gigli, Gianluigi ;
Caielli, Simone ;
Cutuli, Daniela ;
Falcone, Marika .
IMMUNOLOGY, 2007, 122 (03) :409-417
[10]   The Effect of Vitamin A Supplementation on Retinoic Acid-Related Orphan Receptor γt (RORγt) and Interleukin-17 (IL-17) Gene Expression in Avonex-Treated Multiple Sclerotic Patients [J].
Honarvar, Niyaz Mohammadzadeh ;
Harirchian, Mohammad Hossein ;
Koohdani, Fariba ;
Siassi, Feridoun ;
Abdolahi, Mina ;
Bitarafan, Sama ;
Salehi, Eisa ;
Sahraian, Mohammad Ali ;
Eshraghian, Mohammad Reza ;
Saboor-Yarghi, Ali Akbar .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2013, 51 (03) :749-753