Circulating serum levels of IL-1ra in patients with relapsing remitting multiple sclerosis are normal during remission phases but significantly increased either during exacerbations or in response to IFN-beta treatment

被引:70
作者
Nicoletti, F
Patti, F
DiMarco, R
Zaccone, P
Nicoletti, A
Meroni, PL
Reggio, A
机构
[1] UNIV MILAN, INST MICROBIOL, I-20122 MILAN, ITALY
[2] UNIV CATANIA, NEUROL INST, I-95124 CATANIA, ITALY
[3] UNIV MILAN, INST INTERNAL MED INFECT DIS & IMMUNOPATHOL, I-20122 MILAN, ITALY
关键词
interferon; interleukins; interleukins 1 receptor antagonist; multiple sclerosis;
D O I
10.1006/cyto.1996.0054
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Interleukin (IL)-1 receptor antagonist (IL-1ra) is a naturally occurring inhibitor of IL-1 which binds to IL-1 receptors without generating immunologic responses, Evidence has recently been provided that the balance between the production of IL-1 and IL-1ra might influence the course of immunoinflammatory diseases such as inflammatory bowel diseases, rheumatoid arthritis (RA) and Lyme arthritis, To assess whether endogenous IL-1ra may also have a role on the course of multiple sclerosis (MS) we presently studied the fluctuation of the serum levels of IL-1ra in patients with relapsing remitting (RR) MS either during remission or exacerbation, Moreover, to evaluate whether the beneficial effect of IFN-beta on the course of MS might also be mediated by an increased production of IL-1ra, we measured the levels of circulating IL-1ra in MS patients prior to and after 6 months of continuous treatment with natural human IFN-beta (6 000 000 IU three times a week for 6 months), Our results demonstrated that, relative to control subjects, IL-1ra serum levels are 'normal' during remitting phases of RR MS but significantly elevated either during exacerbations or in response to IFN-beta treatment. (C) 1996 Academic Press Limited
引用
收藏
页码:395 / 400
页数:6
相关论文
共 50 条
[1]   SUPPRESSION OF EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS BY INTERFERON [J].
ABREU, SL .
IMMUNOLOGICAL COMMUNICATIONS, 1982, 11 (01) :1-7
[2]   INHIBITION OF PASSIVE LOCALIZED EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS BY INTERFERON [J].
ABREU, SL ;
TONDREAU, J ;
LEVINE, S ;
SOWINSKI, R .
INTERNATIONAL ARCHIVES OF ALLERGY AND APPLIED IMMUNOLOGY, 1983, 72 (01) :30-33
[3]   PATHOLOGY, HISTOCHEMISTRY AND IMMUNOCYTOCHEMISTRY OF LESIONS IN ACUTE MULTIPLE-SCLEROSIS [J].
ADAMS, CWM ;
POSTON, RN ;
BUK, SJ .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1989, 92 (2-3) :291-306
[4]   INTERFERON-BETA IMPAIRS INDUCTION OF HLA-DR ANTIGEN EXPRESSION IN CULTURED ADULT HUMAN ASTROCYTES [J].
BARNA, BP ;
CHOU, SM ;
JACOBS, B ;
YENLIEBERMAN, B ;
RANSOHOFF, RM .
JOURNAL OF NEUROIMMUNOLOGY, 1989, 23 (01) :45-53
[5]   CYTOKINES AND NATURAL REGULATORS OF CYTOKINES [J].
BENDTZEN, K .
IMMUNOLOGY LETTERS, 1994, 43 (1-2) :111-123
[6]   IMMUNE HORMONES (CYTOKINES) - PATHOGENIC ROLE IN AUTOIMMUNE RHEUMATIC AND ENDOCRINE DISEASES [J].
BENDTZEN, K .
AUTOIMMUNITY, 1989, 2 (02) :177-189
[7]  
CAMENGA DL, 1986, ARCH NEUROL-CHICAGO, V43, P1239
[8]  
CASINIRAGGI V, 1995, J IMMUNOL, V154, P2434
[9]  
CHOMARAT P, 1995, J IMMUNOL, V154, P1432
[10]   INTERLEUKIN-1 (IL-1) GENE-EXPRESSION, SYNTHESIS, AND EFFECT OF SPECIFIC IL-1 RECEPTOR BLOCKADE IN RABBIT IMMUNE-COMPLEX COLITIS [J].
COMINELLI, F ;
NAST, CC ;
CLARK, BD ;
SCHINDLER, R ;
LLERENA, R ;
EYSSELEIN, VE ;
THOMPSON, RC ;
DINARELLO, CA .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (03) :972-980