Interferon beta results in immediate reduction of contrast-enhanced MRI lesions in multiple sclerosis patients followed by weekly MRI

被引:69
作者
Calabresi, PA
Stone, LA
Bash, CN
Frank, JA
McFarland, HF
机构
[1] NIH,LAB DIAGNOST RADIOL RES,OFF DIRECTOR,BETHESDA,MD 20892
[2] MAYO CLIN SCOTTSDALE,DEPT NEUROL,SCOTTSDALE,AZ
关键词
D O I
10.1212/WNL.48.5.1446
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Interferon beta-1a and -1b reduce the frequency and severity of clinical exacerbations, and reduce both T-2-weighted and contrast-enhanced MRI activity in patients with multiple sclerosis (MS). Several recent reports suggest that at the initiation of treatment there may be transient worsening of symptoms associated with the induction of interferon gamma-secreting cells. We studied eight MS patients with weekly brain MRI's after starting interferon beta treatment, and found immediate reduction in the number of contrast-enhancing lesions. Several patients did experience recurrence of previous symptoms without concomitant opening of the blood brain barrier on contrast-enhanced MRI. These data suggest that the symptoms described after the initiation of interferon beta are not associated with new disease activity, but rather may be related to preexisting lesions. This has implications for both understanding the immunopathogenesis of the disease and for its treatment.
引用
收藏
页码:1446 / 1448
页数:3
相关论文
共 10 条
[1]   A CORRELATIVE TRIAD OF GADOLINIUM-DTPA MRI, EDSS, AND CSF-MBP IN RELAPSING MULTIPLE-SCLEROSIS PATIENTS TREATED WITH HIGH-DOSE INTRAVENOUS METHYLPREDNISOLONE [J].
BARKHOF, F ;
FREQUIN, STFM ;
HOMMES, OR ;
LAMERS, K ;
SCHELTENS, P ;
VANGEEL, WJA ;
VALK, J .
NEUROLOGY, 1992, 42 (01) :63-67
[2]   Interferon-gamma-secreting cells in multiple sclerosis patients treated with interferon beta-1b [J].
Dayal, AS ;
Jensen, MA ;
Lledo, A ;
Arnason, BGW .
NEUROLOGY, 1995, 45 (12) :2173-2177
[3]  
KURTZKE JF, 1983, NEUROLOGY, V33, P1444, DOI 10.1212/WNL.33.11.1444
[4]   CYTOKINE-REGULATED ADHESION BETWEEN ENCEPHALITOGENIC T-LYMPHOCYTES AND CEREBROVASCULAR ENDOTHELIAL-CELLS [J].
MCCARRON, RM ;
WANG, L ;
RACKE, MK ;
MCFARLIN, DE ;
SPATZ, M .
JOURNAL OF NEUROIMMUNOLOGY, 1993, 43 (1-2) :23-30
[5]   INTERFERON BETA-1B IS EFFECTIVE IN RELAPSING-REMITTING MULTIPLE-SCLEROSIS .2. MRI ANALYSIS RESULTS OF A MULTICENTER, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL [J].
PATY, DW ;
LI, DKB ;
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 .
NEUROLOGY, 1993, 43 (04) :662-667
[6]   NEW DIAGNOSTIC-CRITERIA FOR MULTIPLE-SCLEROSIS - GUIDELINES FOR RESEARCH PROTOCOLS [J].
POSER, CM ;
PATY, DW ;
SCHEINBERG, L ;
MCDONALD, WI ;
DAVIS, FA ;
EBERS, GC ;
JOHNSON, KP ;
SIBLEY, WA ;
SILBERBERG, DH ;
TOURTELLOTTE, WW .
ANNALS OF NEUROLOGY, 1983, 13 (03) :227-231
[7]   The phosphodiesterase inhibitor pentoxifylline reduces early side effects of interferon-beta 1b treatment in patients with multiple sclerosis [J].
Rieckmann, P ;
Weber, F ;
Gunther, A ;
Poser, S .
NEUROLOGY, 1996, 47 (02) :604-604
[8]   DOES INTERFERON-BETA CAUSE INITIAL EXACERBATION OF MULTIPLE-SCLEROSIS [J].
RUDGE, P ;
MILLER, D ;
CRIMLISK, H ;
THORPE, J .
LANCET, 1995, 345 (8949) :580-580
[9]   THE EFFECT OF INTERFERON-BETA ON BLOOD-BRAIN-BARRIER DISRUPTIONS DEMONSTRATED BY CONTRAST-ENHANCED MAGNETIC-RESONANCE-IMAGING IN RELAPSING-REMITTING MULTIPLE-SCLEROSIS [J].
STONE, LA ;
FRANK, JA ;
ALBERT, PS ;
BASH, C ;
SMITH, ME ;
MALONI, H ;
MCFARLAND, HF .
ANNALS OF NEUROLOGY, 1995, 37 (05) :611-619
[10]  
The IFNB Multiple Sclerosis Study Group, 1993, NEUROLOGY, V43, P655