Disease Control in RRMS Transferring Treatment From Natalizumab to Fingolimod

The risk of progressive multifocal leukoencephalopathy (PML) upon treatment with natalizumab increases over time, at least into the 3rd year of therapy. Many Multiple Sclerosis (MS) patients who are currently being treated with natalizumab, as well as their physicians, are looking for alternative MS treatments, fingolimod being one. In transferring patients from natalizumab to fingolimod, it is not known if their co-administration leads to an increased risk of adverse effects due to a shared feature that both have immunomodulation as a mechanism of action. Therefore a sufficient washout period after natalizumab discontinuation and fingolimod initiation is desirable. However, this has to be balanced with the increasing risk over time of recurring disease activity while patients are untreated. This study prospectively evaluates how safe it is to switch patients from natalizumab to fingolimod treatment following cessation of natalizumab treatment, in a cohort of RRMS patients. Safety of the proposed transition paradigms is defined as both traditional safety measures but also recurrence of disease activity during a washout period of 8 weeks after the cessation of natalizumab treatment followed by fingolimod treatment initiation. An interim analysis of the first 15 patients revealed a clinical and MRI activity in 38.5 and 64.3% respectively. Therefore a shorter interval was defined for any subject entering into this study after october 2013: the interval was defined to be 4 weeks for those patients. Overall, the study aims to provide guidance to physicians on the management of natalizumab-treated patients for whom a transition to fingolimod treatment is considered an appropriate treatment alternative. An evidence based rationale for changing to a 4 or 8 week wash out period is not possible due to missing evidence. Due to the known risk of PML for patients being treated with natalizumab for more than 2 years, starting fingolimod during natalizumab therapy seems to be inappropriate, as an elevated risk for JC Virus (JCV) manifestation could be expected in this constellation. On the other hand considerable shortening of the 8-weeks interval could be favorable to prevent clinical and MRI activity. An interval of 4 weeks between last dose of natalizumab and first dose of fingolimod seemed to be an appropriate compromise to balance risks and benefits of this treatment transition. Fingolimod and Natalizumab are influencing the immune system in completely different ways. It is therefore highly interesting not only to monitor clinical disease activity and MRI activity, but also to study immunological responses during the switching phase of both drugs. The change of therapy from natalizumab to fingolimod poses possible risks. On the one hand MS could reactivate if the start of fingolimod is delayed too long, on the other hand infectious problems could emerge if fingolimod is started early and the patient is treated with two concomitant immunomodulators. Analyzing the immune response during the critical Switch period may help to identify markers that predict recrudescence of disease activity or a severe suppression of the immune response. It is known that natalizumab can block migration of lymphocytes via endothelial cells by interaction with integrins. More recently, it has been described that natalizumab influences also gene expression profiles in lymphocytes and that the blockade of migration over endothelial cells might not be as constant as the clinical effect predicts. In contrast to natalizumab, fingolimod blocks egress of lymphocytes from secondary lymphoid organs (SLO) such as lymph nodes. This effect is mediated by functional antagonization sphingosine-1-phosphate (S1P) receptors on lymphocytes by fingolimod. Due to a different expression of lymph node homing receptors naïve and central memory T-cells regularly circulate to SLO and are consequently more prone to sequestration to SLO than effector memory cells that do not circulate to SLO on a regular basis. This is reflected by a decrease of naïve and central memory cells and a relative increase of effector memory cells in peripheral blood of fingolimod treated patients. So far, the effect of a concomitant treatment of natalizumab and fingolimod on the immune system has not been studied. The different aspects of immune modulation of both drugs will be studied. At baseline and then at early follow-up visit (8, 12, 16, 20 weeks) we aim to: * assess alterations of the composition of myeloid cells and lymphocyte subpopulations (i.e. naïve, central memory and effector memory and regulatory T cells, B cells) and adhesion molecule expression in peripheral blood * measure autoantigen specific T cell proliferation and Interferon gamma (IFNγ) production * characterize transcriptomics alterations (including messenger ribonucleic acid (mRNA) and small non-coding RNA expression) in lymphocytes of MS-patients * assess changes in plasma cytokine, chemokine, and Matrix metalloproteinase levels * assess the migratory capacity of peripheral blood mononuclear cells (PBMCs) For the patients being recruited after october 2013 with a shorter wash out period, the neuroimmunological analysis has been omitted.