Literature DB >> 15693804

IL-10 promoter haplotype influence on interferon treatment response in multiple sclerosis.

S Wergeland1, A Beiske, H Nyland, H Hovdal, D Jensen, J P Larsen, T H Marøy, A-I Smievoll, C A Vedeler, K-M Myhr.   

Abstract

The level of interleukin-10 (IL-10) expression is related to polymorphisms -1082 (G/A), -819 (T/C) and -592 (A/C) in the promoter region of the IL-10 gene, which constitute three haplotypes, GCC, ATA, and ACC. The ATA (a non-GCC) haplotype, which is associated with low IL-10 expression, has been shown to improve interferon (IFN) treatment response in hepatitis C. We analysed the distribution of IL-10 promoter haplotype combinations to determine whether they could influence initial IFN treatment response in 63 patients with relapsing-remitting multiple sclerosis (MS). The patients were grouped into non-GCC or GCC haplotypes, and the clinical and magnetic resonance imaging (MRI) disease activity was compared in the two groups. During the first 6 months of treatment, MS patients with non-GCC haplotypes experienced fewer new MRI T1-contrast enhancing lesions [0.77+/-0.36 (SEM)] than patients with the GCC haplotype (2.45+/-0.57) (P=0.05, Mann-Whitney U test). No differences were detected on clinical disease activity. The results suggest an influence of IL-10 promoter polymorphisms on IFN treatment response in MS.

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Year:  2005        PMID: 15693804     DOI: 10.1111/j.1468-1331.2004.01102.x

Source DB:  PubMed          Journal:  Eur J Neurol        ISSN: 1351-5101            Impact factor:   6.089


  7 in total

1.  Cytokine changes during interferon-beta therapy in multiple sclerosis: correlations with interferon dose and MRI response.

Authors:  Jerome J Graber; David Ford; Min Zhan; Gordon Francis; Hillel Panitch; Suhayl Dhib-Jalbut
Journal:  J Neuroimmunol       Date:  2007-02-27       Impact factor: 3.478

2.  Genetic polymorphisms, their allele combinations and IFN-beta treatment response in Irish multiple sclerosis patients.

Authors:  Catherine O'Doherty; Alexander Favorov; Shirley Heggarty; Colin Graham; Olga Favorova; Michael Ochs; Stanley Hawkins; Michael Hutchinson; Killian O'Rourke; Koen Vandenbroeck
Journal:  Pharmacogenomics       Date:  2009-07       Impact factor: 2.533

Review 3.  Is the IL-10 promoter polymorphism at position -592 associated with immune system-related diseases?

Authors:  Mojgan Noroozi Karimabad; Mohammad Kazemi Arababadi; Elham Hakimizadeh; Hassan Yousefi Daredori; Mahmood Nazari; Gholamhossein Hassanshahi; Derek Kennedy
Journal:  Inflammation       Date:  2013-02       Impact factor: 4.092

4.  Candidate gene study of TRAIL and TRAIL receptors: association with response to interferon beta therapy in multiple sclerosis patients.

Authors:  Carlos López-Gómez; Almudena Pino-Ángeles; Teresa Órpez-Zafra; María Jesús Pinto-Medel; Begoña Oliver-Martos; Jesús Ortega-Pinazo; Carlos Arnáiz; Cristina Guijarro-Castro; Jezabel Varadé; Roberto Álvarez-Lafuente; Elena Urcelay; Francisca Sánchez-Jiménez; Óscar Fernández; Laura Leyva
Journal:  PLoS One       Date:  2013-04-29       Impact factor: 3.240

Review 5.  Endogenous, or therapeutically induced, type I interferon responses differentially modulate Th1/Th17-mediated autoimmunity in the CNS.

Authors:  Ulrich Kalinke; Marco Prinz
Journal:  Immunol Cell Biol       Date:  2012-03-20       Impact factor: 5.126

Review 6.  Pharmacogenetic Biomarkers to Predict Treatment Response in Multiple Sclerosis: Current and Future Perspectives.

Authors:  Patricia K Coyle
Journal:  Mult Scler Int       Date:  2017-07-19

Review 7.  Pharmacogenomics of Multiple Sclerosis: A Systematic Review.

Authors:  Keli Hočevar; Smiljana Ristić; Borut Peterlin
Journal:  Front Neurol       Date:  2019-02-26       Impact factor: 4.003

  7 in total

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