Different patterns of activation markers expression and CD4+T-cell responses to ex vivo stimulation in patients with clinically quiescent multiple sclerosis (MS)

被引:16
作者
Kosmaczewska, A.
Bilinska, M.
Ciszak, L.
Noga, L.
Pawlak, E.
Szteblich, A.
Podemski, R.
Frydecka, I.
机构
[1] Polish Acad Sci, Inst Immunol & Expt Therapy, Dept Expt Therapy, Immunopathol Lab, PL-53114 Wroclaw, Poland
[2] Wroclaw Med Univ, Dept Neurol, PL-50420 Wroclaw, Poland
[3] Wroclaw Med Univ, Dept Hematol, PL-50420 Wroclaw, Poland
[4] Wroclaw Med Univ, Dept Pathophysiol, PL-50420 Wroclaw, Poland
关键词
multiple sclerosis; remission; CTLA-4; IFN-gamma; activated CD4+T cells; sCTLA-4;
D O I
10.1016/j.jneuroim.2007.06.021
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Patients with relapsing-remitting (RR) and secondary progressive (SP) forms of multiple sclerosis (MS), although in long-term clinical remission, showed different patterns of increased expressions of the activation markers: CD69, CD40L, and both membrane/surface and cytoplasmic CTLA-4 (mCTLA-4 and cCTLA-4, respectively) in freshly isolated peripheral blood (PB) CD4+ T cells compared with controls. Also observed were dysregulated responses to ex vivo stimulation in both groups of MS patients accompanied by increased IFN-gamma synthesis. Our findings may suggest that the mechanisms leading to each clinical form of the disease may be heterogeneous. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:137 / 146
页数:10
相关论文
共 64 条
[51]   THE FUNCTION OF THE CD2 PROTEIN IS ABNORMAL IN MULTIPLE-SCLEROSIS [J].
REDER, AT ;
ARNASON, BGW ;
MAIMONE, D ;
ROHWERNUTTER, D .
JOURNAL OF AUTOIMMUNITY, 1991, 4 (03) :479-491
[52]   Multiple sclerosis severity score -: Using disability and disease duration to rate disease severity [J].
Roxburgh, RHSR ;
Seaman, SR ;
Masterman, T ;
Hensiek, AE ;
Sawcer, SJ ;
Vukusic, S ;
Achiti, I ;
Confavreux, C ;
Coustans, M ;
le Page, E ;
Edan, G ;
McDonnell, GV ;
Hawkins, S ;
Trojano, M ;
Liguori, M ;
Cocco, E ;
Marrosu, MG ;
Tesser, F ;
Leone, MA ;
Weber, A ;
Zipp, F ;
Miterski, B ;
Epplen, JT ;
Oturai, A ;
Sorensen, PS ;
Celius, EG ;
Lara, NT ;
Montalban, X ;
Villoslada, P ;
Silva, AM ;
Marta, M ;
Leite, I ;
Dubois, B ;
Rubio, J ;
Butzkueven, H ;
Kilpatrick, T ;
Mycko, MP ;
Selmaj, KW ;
Rio, ME ;
Sá, M ;
Salemi, G ;
Savettieri, G ;
Hillert, J ;
Compston, DAS .
NEUROLOGY, 2005, 64 (07) :1144-1151
[53]   IN-VITRO AND IN-VIVO INHIBITION OF MITOGEN-DRIVEN T-CELL ACTIVATION BY RECOMBINANT INTERFERON-BETA [J].
RUDICK, RA ;
CARPENTER, CS ;
COOKFAIR, DL ;
TUOHY, VK ;
RANSOHOFF, RM .
NEUROLOGY, 1993, 43 (10) :2080-2087
[54]   Serum soluble CTLA-4 levels are increased in diffuse cutaneous systemic sclerosis [J].
Sato, S ;
Fujimoto, M ;
Hasegawa, M ;
Komura, K ;
Yanaba, K ;
Hayakawa, I ;
Matsushita, T ;
Takehara, K .
RHEUMATOLOGY, 2004, 43 (10) :1261-1266
[55]   CD4 αβ T lymphocytes express high levels of the T lymphocyte antigen CTLA-4 (CD152) in acute malaria [J].
Schlotmann, T ;
Waase, I ;
Jülch, C ;
Klauenberg, U ;
Müller-Myhsok, B ;
Dietrich, M ;
Fleischer, B ;
Bröker, BM .
JOURNAL OF INFECTIOUS DISEASES, 2000, 182 (01) :367-370
[56]  
Steiner K, 1999, CLIN EXP IMMUNOL, V115, P451
[57]  
Teleshova N, 2000, SCAND J IMMUNOL, V51, P312
[58]   LOSS OF CTLA-4 LEADS TO MASSIVE LYMPHOPROLIFERATION AND FATAL MULTIORGAN TISSUE DESTRUCTION, REVEALING A CRITICAL NEGATIVE REGULATORY ROLE OF CTLA-4 [J].
TIVOL, EA ;
BORRIELLO, F ;
SCHWEITZER, AN ;
LYNCH, WP ;
BLUESTONE, JA ;
SHARPE, AH .
IMMUNITY, 1995, 3 (05) :541-547
[59]  
Van Parijs L, 1998, SCIENCE, V280, P243
[60]  
VAN SG, 1990, J IMMUNOL, V144, P4579