Multiple sclerosis: glatiramer acetate induces anti-inflammatory T cells in the cerebrospinal fluid

被引:32
作者
Hestvik, A. L. K. [1 ]
Skorstad, G. [2 ]
Price, D. A. [3 ]
Vartdal, F. [1 ]
Holmoy, T. [1 ,2 ]
机构
[1] Rikshosp Radiumhosp, Inst Immunol, Fac Med, Oslo, Norway
[2] Ullevaal Univ Hosp, Dept Neurol, Oslo, Norway
[3] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DU, England
关键词
multiple sclerosis; immunology; glatiramer acetate; disease modifying therapies;
D O I
10.1177/1352458508089411
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Glatiramer acetate (GA) is believed to induce GA-reactive T cells that secrete anti-inflammatory cytokines at the site of inflammation in multiple sclerosis (MS). However, GA-reactive T cells have not been established from the intrathecal compartment of MS patients, and intrathecal T cells may differ from T cells in blood. Here, we compared the phenotype of GA-reactive T cells from the cerebrospinal fluid (CSF) and blood of five MS patients treated with GA for 3-36 months, and in three of these patients also before treatment. From the CSF of these patients, all 22 T cell lines generated before and all 38 T cell lines generated during treatment were GA-reactive. GA treatment induced a more pronounced anti-inflammatory profile of GA-reactive T cell lines from CSF than from blood. While GA-reactive T cell clones from CSF were restricted by either human leukocyte antigen (HLA) -DR or HLA-DP, only HLA-DR restricted GA-reactive T cell clones were detected in blood. No cross reactivity with myelin proteins was detected in GA-reactive T cell lines or clones from CSF. These results suggest that a selected subset of GA-reactive T cells are present in the intrathecal compartment, and support an anti-inflammatory mechanism of action for GA.
引用
收藏
页码:749 / 758
页数:10
相关论文
共 50 条
  • [2] Renewal of the T-cell compartment in multiple sclerosis patients treated with glatiramer acetate
    Chiarini, M.
    Sottini, A.
    Ghidini, C.
    Zanotti, C.
    Serana, F.
    Rottoli, M.
    Zaffaroni, M.
    Bergamaschi, R.
    Cordioli, C.
    Capra, R.
    Imberti, L.
    MULTIPLE SCLEROSIS JOURNAL, 2010, 16 (02) : 218 - 227
  • [3] In vitro evidence that subcutaneous administration of glatiramer acetate induces hyporesponsive T cells in patients with multiple sclerosis
    Schmied, M
    Duda, PW
    Krieger, JI
    Trollmo, C
    Hafler, DA
    CLINICAL IMMUNOLOGY, 2003, 106 (03) : 163 - 174
  • [4] Biological activity of glatiramer acetate on Treg and anti-inflammatory monocytes persists for more than 10 years in responder multiple sclerosis patients
    Spadaro, Michela
    Montarolo, Francesca
    Perga, Simona
    Martire, Serena
    Brescia, Federica
    Malucchi, Simona
    Bertolotto, Antonio
    CLINICAL IMMUNOLOGY, 2017, 181 : 83 - 88
  • [5] Glatiramer acetate in multiple sclerosis: A review
    Ruggieri, Maddalena
    Avolio, Carlo
    Livrea, Paolo
    Trojano, Maria
    CNS DRUG REVIEWS, 2007, 13 (02): : 178 - 191
  • [6] Glatiramer acetate for the treatment of multiple sclerosis
    Wolinsky, JS
    EXPERT OPINION ON PHARMACOTHERAPY, 2004, 5 (04) : 875 - 891
  • [7] Long-term therapy with glatiramer acetate in multiple sclerosis: effect on T-cells
    Ragheb, S
    Abramczyk, S
    Lisak, D
    Lisak, R
    MULTIPLE SCLEROSIS JOURNAL, 2001, 7 (01) : 43 - 47
  • [8] Dendritic cell, monocyte and T cell activation and response to glatiramer acetate in multiple sclerosis
    Sellebjerg, F.
    Hesse, D.
    Limborg, S.
    Lund, H.
    Sondergaard, H. B.
    Krakauer, M.
    Sorensen, P. S.
    MULTIPLE SCLEROSIS JOURNAL, 2013, 19 (02) : 179 - 187
  • [9] Glatiramer acetate for multiple sclerosis
    La Mantia, Loredana
    Munari, Luca M.
    Lovati, Roberta
    COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2010, (05):
  • [10] Immunoregulatory T cells in multiple sclerosis and the effect of interferon beta and glatiramer acetate treatment on T cell subpopulations
    Praksova, Petra
    Stourac, Pavel
    Bednarik, Josef
    Vlckova, Eva
    Mikulkova, Zuzana
    Michalek, Jaroslav
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2012, 319 (1-2) : 18 - 23