Literature DB >> 10871787

Serum auto antibodies presence in multiple sclerosis patients treated with beta-interferon 1a and 1b.

L Speciale1, M Saresella, D Caputo, S Ruzzante, R Mancuso, M G Calvo, F R Guerini, P Ferrante.   

Abstract

To verify the possible effect of IFN-beta treatment on auto antibodies development in multiple sclerosis (MS) we studied 69 MS patients before and during the treatment with IFN-beta 1b (n=35) and IFN-beta 1a (n=20) for 27 and 12 months respectively, and, as controls, 14 untreated MS patients. The serum, collected every 3 months from all the patients, was investigated for the presence of antinuclear (ANA), anti-smooth muscle (ASMA), anti-mitochondrial (AMA), anti-native DNA (nDNA) anti-cardiolipin (aCL), anti-parietal cells (APCA), anti-microsomal (AMC) and anti-tireoglobulin (ATG) antibodies. Among the IFN-beta 1b-treated MS patients an increase of the frequency and of the level of ANA, AMC and ATG was observed. ASMA and ANA antibodies were already present in about 45% of the MS patients before the treatment and fluctuated over the time. In one patient the treatment was interrupted after 6 months because of the occurrence of high ASMA level and of an autoimmune hepatitis. The data obtained in the smaller number of MS patients treated with IFN-beta 1a were very similar. No increase in aCL level was observed during both the IFN treatments. Our results indicate that the treatment with IFN-beta induces an increase of AMC and ATG antibodies in MS patients and confirm that, although rare, autoimmune diseases could be observed. The possible effect of these auto antibodies on the treatment efficacy and on MS clinical course need to be further investigated.

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Year:  2000        PMID: 10871787

Source DB:  PubMed          Journal:  J Neurovirol        ISSN: 1355-0284            Impact factor:   2.643


  11 in total

1.  Remission of a CNS inflammatory disease accompanied by newly developed ANA and arthropathy during treatment with IFN-beta.

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2.  Glatiramer acetate induced acute exacerbation of autoimmune hepatitis in a patient with multiple sclerosis.

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Journal:  J Neurol       Date:  2007-03-12       Impact factor: 4.849

3.  Autoimmune hepatitis induced by a single injection of interferon-β 1a in a patient with multiple sclerosis.

Authors:  Hiroki Yamaguchi; Kenji Sakai; Yoshinori Goto; Masahito Yamada
Journal:  J Neurol       Date:  2018-05-29       Impact factor: 4.849

4.  High frequency of antiphospholipid antibodies in relapse of multiple sclerosis: a possible indicator of inflammatory-thrombotic processes.

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5.  Clinical characteristics of autoimmune disorders in the central nervous system associated with myasthenia gravis.

Authors:  Kimitoshi Kimura; Yoichiro Okada; Chihiro Fujii; Kenichi Komatsu; Ryosuke Takahashi; Sadayuki Matsumoto; Takayuki Kondo
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6.  Autoantibody synthesis in primary progressive multiple sclerosis patients treated with interferon beta-1b.

Authors:  Andreas Bitsch; Alexander Dressel; Kathrin Meier; Timon Bogumil; Florian Deisenhammer; Hayrettin Tumani; Bernd Kitze; Sigrid Poser; Frank Weber
Journal:  J Neurol       Date:  2004-12       Impact factor: 4.849

7.  Myasthenia Gravis during the Course of Neuromyelitis Optica.

Authors:  Masoud Etemadifar; Seyed-Hossein Abtahi; Alireza Dehghani; Mohammad-Ali Abtahi; Mojtaba Akbari; Nasim Tabrizi; Tannaz Goodarzi
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Review 8.  Regulatory T cells in multiple sclerosis and myasthenia gravis.

Authors:  K M Danikowski; S Jayaraman; B S Prabhakar
Journal:  J Neuroinflammation       Date:  2017-06-09       Impact factor: 8.322

9.  Presentation and outcomes with clinically apparent interferon beta hepatotoxicity.

Authors:  Robert J Fontana; Paul Hayashi; Herbert L Bonkovsky; David E Kleiner; Sweta Kochhar; Jiezhun Gu; Marwan Ghabril
Journal:  Dig Dis Sci       Date:  2013-02-02       Impact factor: 3.487

10.  Multiple sclerosis presented as clinically isolated syndrome: the need for early diagnosis and treatment.

Authors:  Sigliti-Henrietta Pelidou; Sotirios Giannopoulos; Sotiria Tzavidi; Georgios Lagos; Athanassios P Kyritsis
Journal:  Ther Clin Risk Manag       Date:  2008-06       Impact factor: 2.423

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