26 May 2015 : Clinical Research
Therapeutic Plasma Exchange in Multiple Sclerosis Patients with Abolished Interferon-beta Bioavailability
Natasa GiedraitieneABCDEF, Gintaras KaubrysADE, Rasa KizlaitieneABD, Loreta BagdonaiteAE, Laimonas GriskeviciusAE, Vilma ValceckieneBE, Mindaugas StoskusBEDOI: 10.12659/MSM.894119
Med Sci Monit 2015; 21:1512-1519
Abstract
BACKGROUND: Neutralizing antibodies (NAb) to interferon-beta (IFN-β) are associated with reduced bioactivity and efficacy of IFN-β in multiple sclerosis (MS). The myxovirus resistance protein A (MxA) gene expression is one of the most appropriate markers of biological activity of exogenous IFN-β. We hypothesized that therapeutic plasma exchange (TPE) can restore the ability of IFN-β to induce the MxA mRNA expression and that maintenance plasmapheresis can sustain the bioavailability of IFN-β.
MATERIAL AND METHODS: Eligible patients underwent 4 primary separate plasma exchange sessions. After the induction TPE sessions, they were transferred to maintenance plasmapheresis. Bioactivity of IFN-β was expressed as in vivo MxA mRNA induction in whole blood using RT-qPCR.
RESULTS: Six patients with low IFN-β bioavailability detected by the MxA mRNA response were included. Four patients became biological responders after induction plasmapheresis. In 2 patients an increase of MxA mRNA expression was found, but the values persisted below the cut-off and the patients remained as “poor biological responders”. The effect of maintenance plasmapheresis was transient: MxA mRNA expression values reverted to the baseline levels after 1–2 months.
CONCLUSIONS: Therapeutic plasma exchange is able to restore the bioavailability of IFN-β in the majority of studied patients, but the effect of TPE on the IFN-β bioavailability was transient.
Keywords: Antibodies, Neutralizing - immunology, Biological Availability, Biomarkers - metabolism, Interferon-beta - pharmacokinetics, Multiple Sclerosis - therapy, Myxovirus Resistance Proteins - metabolism, Pilot Projects, Plasma Exchange - methods, Plasmapheresis - methods, Reverse Transcriptase Polymerase Chain Reaction
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