Multiple sclerosis patients with anti-lipid oligoclonal IgM show early favourable response to immunomodulatory treatment

被引:20
作者
Garcia-Barragan, N. [1 ]
Villar, L. M. [2 ]
Espino, M. [2 ]
Sadaba, M. C. [1 ]
Gonzalez-Porque, P. [2 ]
Alvarez-Cermeno, J. C. [1 ,3 ]
机构
[1] Hosp Ramon & Cajal, Serv Neurol, Dept Neurol, E-28034 Madrid, Spain
[2] Hosp Ramon & Cajal, Dept Immunol, E-28034 Madrid, Spain
[3] Univ Alcala de Henares, Dept Med, Madrid, Spain
关键词
disease modifying therapies; IgM; immunomodulation; multiple sclerosis; oligoclonal bands; INTERFERON-BETA TREATMENT; CLINICALLY DEFINITE; DISEASE COURSE; DIAGNOSTIC-CRITERIA; PREDICT CONVERSION; CORRELATE; LESIONS; DISABILITY; GUIDELINES; THERAPY;
D O I
10.1111/j.1468-1331.2008.02504.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Interferon beta and Glatiramer acetate are safe immunomodulatory treatments (IT) for multiple sclerosis (MS), but not always effective. New drugs are available, although they show more side-effects and unknown long-term safety profile. Anti-lipid oligoclonal IgM bands (OCMB) distinguish MS patients with early aggressive course. We prospectively studied if IT are effective in these patients or if they are candidates for more aggressive drugs as first therapeutic option. Seventy-five clinically isolated syndrome patients were studied. OCMB and conversion to MS were assessed. Patients suffering at least two demyelinating events within 3 years were considered eligible to start IT. Eighteen patients showed OCMB (M+) and 57 lacked them (M-). All M+ patients and only 25 M- patients were treated. The other 32 M- patients suffered less MS attacks than those required to initiate treatment. IT similarly reduced relapse rate in both treated groups (P < 0.0001) and reduced Expanded Disability Status Scale (EDSS) progression in M+ patients, whose EDSS score had significantly increased before treatment. EDSS did not change in M- patients during follow-up, regardless if they were treated or not. Oligoclonal IgM bands identify MS patients who are candidates for early immunomodulatory treatment as IT improves their initial aggressive disease course.
引用
收藏
页码:380 / 385
页数:6
相关论文
共 42 条
[1]
Comparison of MRI criteria at first presentation to predict conversion to clinically definite multiple sclerosis [J].
Barkhof, F ;
Filippi, M ;
Miller, DH ;
Scheltens, P ;
Campi, A ;
Polman, CH ;
Comi, G ;
Ader, HJ ;
Losseff, N ;
Valk, J .
BRAIN, 1997, 120 :2059-2069
[2]
Development of biomarkers in multiple sclerosis [J].
Bielekova, B ;
Martin, R .
BRAIN, 2004, 127 :1463-1478
[3]
Homogeneity of active demyelinating lesions in established multiple sclerosis [J].
Breij, Esther C. W. ;
Brink, Bianca P. ;
Veerhuis, Rob ;
Van den Berg, Christa ;
Vloet, Rianka ;
Yan, Riqiang ;
Dijkstra, Christine D. ;
Van der Valk, Paul ;
Boe, Lars .
ANNALS OF NEUROLOGY, 2008, 63 (01) :16-25
[4]
TRAIL, CXCL10 and CCL2 levels during long-term Interferon-β treatment of patients with multiple sclerosis correlate with flu-like adverse effects but do not predict therapeutic response [J].
Buttmann, Mathias ;
Merzyn, Comelia ;
Hofstetter, Harald H. ;
Rieckmann, Peter .
JOURNAL OF NEUROIMMUNOLOGY, 2007, 190 (1-2) :170-176
[5]
Genome-wide pharmacogenomic analysis of the response to interferon β therapy in multiple sclerosis [J].
Byun, Esther ;
Caillier, Stacy J. ;
Montalban, Xavier ;
Villoslada, Pablo ;
Fernandez, Oscar ;
Brassat, David ;
Comabella, Manuel ;
Wang, Joanne ;
Barcellos, Lisa F. ;
Baranzini, Sergio E. ;
Oksenberg, Jorge R. .
ARCHIVES OF NEUROLOGY, 2008, 65 (03) :337-E2
[6]
Patterns of cerebrospinal fluid pathology correlate with disease progression in multiple sclerosis [J].
Cepok, S ;
Jacobsen, M ;
Schock, S ;
Omer, B ;
Jaekel, S ;
Böddeker, I ;
Oertel, WH ;
Sommer, N ;
Hemmer, B .
BRAIN, 2001, 124 :2169-2176
[7]
Short-lived plasma blasts are the main B cell effector subset during the course of multiple sclerosis [J].
Cepok, S ;
Rosche, B ;
Grummel, V ;
Vogel, F ;
Zhou, D ;
Sayn, J ;
Sommer, N ;
Hartung, HP ;
Hemmer, B .
BRAIN, 2005, 128 :1667-1676
[8]
Effect of early interferon treatment on conversion to definite multiple sclerosis:: a randomised study [J].
Comi, G ;
Filippi, M ;
Barkhof, F ;
Durelli, L ;
Edan, G ;
Fernández, O ;
Hartung, HP ;
Seeldrayers, P ;
Sorensen, PS ;
Rovaris, M ;
Martinelli, V ;
Hommes, OR .
LANCET, 2001, 357 (9268) :1576-1582
[9]
Multiple sclerosis [J].
Compston, A ;
Coles, A .
LANCET, 2002, 359 (9313) :1221-1231
[10]
Axonal damage in acute multiple sclerosis lesions [J].
Ferguson, B ;
Matyszak, MK ;
Esiri, MM ;
Perry, VH .
BRAIN, 1997, 120 :393-399