Single-cell analysis of cytokine production shows different immune profiles in multiple sclerosis patients with active or quiescent disease

被引:49
作者
Clerici, M
Saresella, M
Trabattoni, D
Speciale, L
Fossati, S
Ruzzante, S
Cavaretta, R
Filippi, M
Caputo, D
Ferrante, P
机构
[1] Univ Milan, DISP LITA Vialba, Cattedra Immunol, I-20157 Milan, Italy
[2] IRCCS, Don C Gnocchi Fdn, Biol Lab, I-20148 Milan, Italy
[3] IRCCS, Don C Gnocchi Fdn, Unit Sclerosi Multipla, I-20148 Milan, Italy
[4] Osped San Raffaele, IRCCS, Neuroimaging Res Unit, Milan, Italy
[5] Univ Milan, Cattedra Virol, I-20157 Milan, Italy
关键词
multiple sclerosis; cell-mediated immunity; cytokines; Th1/Th2; interferon beta;
D O I
10.1016/S0165-5728(01)00431-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Peripheral blood mononuclear cells of multiple sclerosis (MS) patients were stimulated with myelin basic protein (MBP) together with anti-CD28 monoclonal antibody and staphylococcal enterotoxin B to optimize cytokine production by antigen-specific cells. Type 1 IL-2, IL-12, IFNgamma) and pro-inflammatory (TNFalpha, IL-1beta, IL-6) cytokines were augmented in CD4 +, CD8 +, and CD14 + cells of acute MS patients and of patients undergoing disease reactivation. These cytokines were reduced in IFNbeta-treated and in stable MS patients; type 2 cytokines (IL-4, IL-10) were increased in these patients. Similar immune profiles are seen in MS patient in whom remission is naturally or pharmacologically (IFNbeta) achieved. Cytokine alterations are particularly evident in CD14 + cells, underlying their critical role in the modulation of the immune response. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:88 / 101
页数:14
相关论文
共 57 条
[1]  
Alleva DG, 1998, J IMMUNOL, V161, P6878
[2]   CYTOKINES - COORDINATORS OF IMMUNE AND INFLAMMATORY RESPONSES [J].
ARAI, K ;
LEE, F ;
MIYAJIMA, A ;
MIYATAKE, S ;
ARAI, N ;
YOKOTA, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1990, 59 :783-836
[3]   Interferon beta in multiple sclerosis [J].
Arnason, BGW .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1996, 81 (01) :1-11
[4]   Transcriptional analysis of multiple sclerosis brain lesions reveals a complex pattern of cytokine expression [J].
Baranzini, SE ;
Elfstrom, C ;
Chang, SY ;
Butunoi, C ;
Murray, R ;
Higuchi, R ;
Oksenberg, JR .
JOURNAL OF IMMUNOLOGY, 2000, 165 (11) :6576-6582
[5]   Superantigens augment antigen-specific Th1 responses by inducing IL-12 production in macrophages [J].
Bright, JJ ;
Xin, ZC ;
Sriram, S .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 65 (05) :665-670
[6]   Interferon-beta(1b) treatment decreases tumor necrosis factor-alpha and increases interleukin-6 production in multiple sclerosis [J].
Brod, SA ;
Marshall, GD ;
Henninger, EM ;
Sriram, S ;
Khan, M ;
Wolinsky, JS .
NEUROLOGY, 1996, 46 (06) :1633-1638
[7]   Regulation of interleukin (IL)-12 receptor β2 subunit expression by endogenous IL-12:: A critical step in the differentiation of pathogenic autoreactive T cells [J].
Chang, JT ;
Shevach, EM ;
Segal, BM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (06) :969-978
[8]  
COSTANTINESCU CS, 2001, CLIN IMMUNOL, V98, P23
[9]   Viruses and multiple sclerosis [J].
Dalgleish, AG .
ACTA NEUROLOGICA SCANDINAVICA, 1997, 95 :8-15
[10]   INTERFERON BETA-1B IS EFFECTIVE IN RELAPSING-REMITTING MULTIPLE-SCLEROSIS - CLINICAL-RESULTS OF A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL [J].
DUQUETTE, P ;
GIRARD, M ;
DESPAULT, L ;
DUBOIS, R ;
KNOBLER, RL ;
LUBLIN, FD ;
KELLEY, L ;
FRANCIS, GS ;
LAPIERRE, Y ;
ANTEL, J ;
FREEDMAN, M ;
HUM, S ;
GREENSTEIN, JI ;
MISHRA, B ;
MULDOON, J ;
WHITAKER, JN ;
EVANS, BK ;
LAYTON, B ;
SIBLEY, WA ;
LAGUNA, J ;
KRIKAWA, J ;
PATY, DW ;
OGER, JJ ;
KASTRUKOFF, LF ;
MOORE, GRW ;
HASHIMOTO, SA ;
MORRISON, W ;
NELSON, J ;
GOODIN, DS ;
MASSA, SM ;
GUTTERIDGE, E ;
ARNASON, BGW ;
NORONHA, A ;
REDER, AT ;
MARTIA, R ;
EBERS, GC ;
RICE, GPA ;
LESAUX, J ;
JOHNSON, KP ;
PANITCH, HS ;
BEVER, CT ;
CONWAY, K ;
WALLENBERG, JC ;
BEDELL, L ;
VANDENNOORT, S ;
WEINSHENKER, B ;
WEISS, W ;
REINGOLD, S ;
PACHNER, A ;
TAYLOR, W .
NEUROLOGY, 1993, 43 (04) :655-661