The cross-reactivity of binding antibodies with different interferon beta formulations used as disease-modifying drugs in multiple sclerosis patients
| Autor: | Alicja Kalinowska-Lyszczarz, Agnieszka Wencel-Warot, Slawomir Michalak, Radoslaw Kazmierski, Marcin Warot |
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| Rok vydání: | 2016 |
| Předmět: |
Adult
Male Observational Study Context (language use) Pilot Projects binding antibodies Cross Reactions multiple sclerosis Antibodies immunology 03 medical and health sciences 0302 clinical medicine Natalizumab Multiple Sclerosis Relapsing-Remitting Antigen Interferon disease modifying therapies medicine Humans Prospective Studies Glatiramer acetate business.industry Multiple sclerosis Interferon beta-1a General Medicine Interferon-beta medicine.disease Fingolimod beta interferon Immunology Female business 030217 neurology & neurosurgery 030215 immunology medicine.drug Interferon beta-1b Research Article |
| Zdroj: | Medicine |
| ISSN: | 1536-5964 |
| Popis: | Interferon beta (IFNb) preparations are commonly used as first-line therapy in relapsing-remitting multiple sclerosis (RRMS). They are, however, characterized by limited efficacy, partly due to the formation of anti-IFNb antibodies in patients. In this pilot study, we assessed with the ELISA method the presence of the binding antibodies (BAbs) against interferon beta after 2 years of therapy with subcutaneous interferon beta 1a (Rebif) in 49 RRMS patients. Antibody levels were established again within 1 year after treatment withdrawal. We used 3 interferons that are commercially available for MS therapy, namely Avonex (Biogen Idec Limited), Rebif (Merck Serono), and Betaferon (Bayer Pharma AG), as antigens. BAbs reacting with Rebif were found in 24.4% to 55% of patients, depending on the units of their expression. The levels of anti-Rebif antibodies remained high in 8 patients and in 4 patients they dropped significantly. Strong correlations were obtained in all assays (anti-Rebif-anti-Avonex, anti-Rebif-anti-Betaferon, and anti-Betaferon-anti-Avonex) and the existence of cross-reactivity in the formation of antibodies against all the tested formulations of interferon beta was confirmed. The levels of BAbs remain significant in the clinical context, and their assessment is the first choice screening; however, methods of BAbs evaluation can be crucial for further decisions. More studies are needed to confirm our results; specifically it would be of interest to evaluate methods of neutralizing antibodies identification, as we only assessed the binding antibodies. Nevertheless, our results support the concept that in interferon nonresponders, that are positive for binding antibodies, switching the therapy to alternative disease-modifying agent (for example glatiramer acetate, fingolimod, or natalizumab) is justified, whereas the switch to another interferon formulation will probably be of no benefit. |
| Databáze: | OpenAIRE |
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