Autoantibodies in multiple sclerosis patients before and during IFN-β1b treatment:: Are they correlated with the occurrence of autoimmune diseases?

被引:31
作者
Verdun, E
Isoardo, G
Oggero, A
Ferrero, B
Ghezzi, A
Montanari, E
Zaffaroni, M
Durelli, L
机构
[1] Univ Turin, Dipartimento Neurosci, Neurol Clin, I-10126 Turin, Italy
[2] Osped Gallarate, Div Neurol, Gallarate, Italy
[3] Osped Fidenza, Div Neurol, Fidenza, Italy
关键词
D O I
10.1089/107999002753536220
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
Autoimmune side effects, namely autoantibody (autoAb) occurrence and thyroid function alteration, have been described during interferon-beta (IFN-beta) treatment for multiple sclerosis (MS). AutoAb occurrence and autoimmune thyroid diseases are also frequently detected in MS patients free of any treatment. The aim of this study was to evaluate the relationship between IFN-beta1b treatment, autoAb occurrence, and autoimmune diseases in MS. Thyroid and liver function and serum autoAb (antithyroid, antinuclear, antiliver, antikidney microsomes, antismooth muscle and parietal cell antigens) occurrence were evaluated in 156 relapsing-remitting MS (RRMS) patients before and every 3 months after starting IFN-beta1b treatment (8 MIU subcutaneously [s.c.] on alternate days). The probability of having liver or thyroid function alteration or autoAb occurrence was analyzed longitudinally with the generalized estimating equations (GEE) approach. At baseline, 16.1% of patients had autoAb. During treatment, autoAb occurred de novo in 7.2% of patients. GEE analysis showed that the probability of having autoAb at any time during IFN-beta1b treatment did not change significantly compared with baseline. AutoAb occurring de novo rarely persisted during treatment and significantly less than those already present at baseline. Positivity for autoAb at baseline or during treatment was not correlated with the development of thyroid or liver function alteration during IFN-beta1b treatment. Our study indicates that IFN-beta treatment is a safe treatment for MS patients, free of risk of autoimmunity and of associated liver or thyroid function alteration.
引用
收藏
页码:245 / 255
页数:11
相关论文
共 52 条
[31]   Medical progress: Multiple sclerosis. [J].
Noseworthy, JH ;
Lucchinetti, C ;
Rodriguez, M ;
Weinshenker, BG .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (13) :938-952
[32]  
PENDER M, 1995, AUTOIMMUNE NEUROLOGI
[33]   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
[34]   Antinuclear antibodies and MRI activity in multiple sclerosis [J].
Pozzilli, C ;
Bastianello, S ;
Gasperini, C ;
Salvetti, M .
NEUROLOGY, 1998, 51 (02) :650-650
[35]   AUTOIMMUNITY AND THYROID-FUNCTION IN PATIENTS WITH CHRONIC ACTIVE HEPATITIS TREATED WITH RECOMBINANT INTERFERON ALPHA-2A [J].
PREZIATI, D ;
LAROSA, L ;
COVINI, G ;
MARCELLI, R ;
RESCALLI, S ;
PERSANI, L ;
DELNINNO, E ;
MERONI, PL ;
COLOMBO, M ;
BECKPECCOZ, P .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1995, 132 (05) :587-593
[36]   AUTOIMMUNITY AFTER ALPHA-INTERFERON THERAPY FOR MALIGNANT CARCINOID-TUMORS [J].
RONNBLOM, LE ;
ALM, GV ;
OBERG, KE .
ANNALS OF INTERNAL MEDICINE, 1991, 115 (03) :178-183
[37]  
ROTI E, 1996, AM J MED, V172, P482
[38]   Occurrence of thyroid autoimmunity and dysfunction throughout a nine-month follow-up in patients undergoing interferon-β therapy for multiple sclerosis [J].
Rotondi, M ;
Oliviero, A ;
Profice, P ;
Mone, CM ;
Biondi, B ;
Del Buono, A ;
Mazziotti, G ;
Sinisi, AM ;
Bellastella, A ;
Carella, C .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 1998, 21 (11) :748-752
[39]   AUTOANTIBODIES AND RESPONSE TO ALPHA-INTERFERON IN PATIENTS WITH CHRONIC VIRAL-HEPATITIS [J].
SARACCO, G ;
TOUSCOZ, A ;
DURAZZO, M ;
ROSINA, F ;
DONEGANI, E ;
CHIANDUSSI, L ;
GALLO, V ;
PETRINO, R ;
DEMICHELI, AG ;
SOLINAS, A ;
DEPLANO, A ;
TOCCO, A ;
COSSU, PA ;
PINTUS, C ;
VERME, G ;
RIZZETTO, M .
JOURNAL OF HEPATOLOGY, 1990, 11 (03) :339-343
[40]  
SCHWID SR, 1997, ARCH NEUROL-CHICAGO, V57, P1169