Current status and future prospective of immunointervention in multiple sclerosis

被引:7
作者
Cavaletti, Guido [1 ]
机构
[1] Univ Milano Bicocca, Dipartimento Neurosci & Tecnol Biomed, I-20052 Monza, MI, Italy
关键词
multiple sclerosis; treatment; inflammation; pathogenesis; immunosuppression;
D O I
10.2174/092986706777935168
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Multiple sclerosis (MS) is a complex neurological disorder characterized by inflammation and degeneration of the central nervous system, primarily involving the white matter. On the basis of a wide body of evidence in experimental models and in affected patients, several attempts to treat MS using drugs which modulate immune reactions have been performed or are currently ongoing. However, it should be stressed that inflammation does not have only a detrimental effect in MS. In fact, parts of the inflammatory events are crucial for the control and conclusion of the acute phase of damage and it is probable that they actually favor regeneration and recovery. Due to the above, several trials with immunosuppressant drugs failed or were suspended because of unexpected worsening of the course of MS. The knowledge of MS immunopathogenesis is so rapidly evolving that any attempt to review it is in some way frustrating. On the other hand, this evolution is at the basis of the several new treatment options which can be hypothesized for this disease. The current status of immunosuppression in MS and the possible future development of MS treatment will be reviewed, with particular reference to those treatments which have already been tested in clinical trials and which are based on sound evidence of a putative interference with specific events occurring in MS, with the sparing of general immunity.
引用
收藏
页码:2329 / 2343
页数:15
相关论文
共 161 条
[1]
CTLA4Ig-mediated blockade of T-cell costimulation in patients with psoriasis vulgaris [J].
Abrams, JR ;
Lebwohl, MG ;
Guzzo, CA ;
Jegasothy, BV ;
Goldfarb, MT ;
Goffe, BS ;
Menter, A ;
Lowe, NJ ;
Krueger, G ;
Brown, MJ ;
Weiner, RS ;
Birkhofer, MJ ;
Warner, GL ;
Berry, KK ;
Linsley, PS ;
Krueger, JG ;
Ochs, HD ;
Kelley, SL ;
Kang, SW .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (09) :1243-1252
[2]
Blockade of T lymphocyte costimulation with cytotoxic T lymphocyte-associated antigen 4-immunoglobulin (CTLA4Ig) reverses the cellular pathology of psoriatic plaques, including the activation of keratinocytes, dendritic cells, and endothelial cells [J].
Abrams, JR ;
Kelley, SL ;
Hayes, E ;
Kikuchi, T ;
Brown, MJ ;
Kang, SW ;
Lebwohl, MG ;
Guzzo, CA ;
Jegasothy, BV ;
Linsley, PS ;
Krueger, JG .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (05) :681-693
[3]
Effect of intravenous immunoglobulin treatment on pregnancy and postpartum-related relapses in multiple sclerosis [J].
Achiron, A ;
Kishner, I ;
Dolev, M ;
Stern, Y ;
Dulitzky, M ;
Schiff, E ;
Achiron, R .
JOURNAL OF NEUROLOGY, 2004, 251 (09) :1133-1137
[4]
Immunotherapeutic approaches in multiple sclerosis [J].
Adorini, L .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2004, 223 (01) :13-24
[5]
Low dose naltrexone therapy in multiple sclerosis [J].
Agrawal, YP .
MEDICAL HYPOTHESES, 2005, 64 (04) :721-724
[6]
[Anonymous], 1999, Neurology, V53, P457
[7]
[Anonymous], COCHRANE DATABASE SY
[8]
Serum MMP-9/TIMP-1 and MMP-2/TIMP-2 ratios in multiple sclerosis: relationships with different magnetic resonance imaging measures of disease activity during IFN-beta-1a treatment [J].
Avolio, C ;
Filippi, M ;
Tortorella, C ;
Rocca, MA ;
Ruggieri, M ;
Agosta, F ;
Tomassini, V ;
Pozzilli, C ;
Stecchi, S ;
Giaquinto, P ;
Livrea, P ;
Trojano, M .
MULTIPLE SCLEROSIS, 2005, 11 (04) :441-446
[9]
Mitoxantrone, a topoisomerase II inhibitor, induces apoptosis of B-chronic lymphocytic leukaemia cells [J].
Bellosillo, B ;
Colomer, D ;
Pons, G ;
Gil, J .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 100 (01) :142-146
[10]
Progressive multifocal leukoencephalopathy and natalizumab - Unforeseen consequences [J].
Berger, JR ;
Koralnik, IJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (04) :414-416