Calorie Restriction in Multiple Sclerosis

Overview

There is a strong relationship between metabolic state and immune tolerance through a direct control exerted on immune cells by specific intracellular nutrient-energy sensors. An increased "metabolic work load" represents a novel issue linking metabolism with loss of self-immune tolerance. Several disease-modifying drugs have been approved for Relapsing-remitting Multiple Sclerosis (RR-MS) treatments and have shown to reduce relapse rates by modulating immune responses; however, their impact on long-term disease progression and accrual of irreversible neurological disability remains largely unclear, underlining the need for novel therapeutic strategies. In this context, both acute fasting (AF) and chronic caloric restriction (CR) have been shown to improve experimental autoimmune encephalomyelitis (EAE). Despite this evidence, no specific studies have been performed to dissect at the cellular level the mechanism of action of CR in the context of autoimmunity and MS. This study aims at investigating this specific point in order to pave the way for a wider utilization of a nutritional approach to alter MS progression and activity. The aim of this study is to improve the outcome of RR-MS and the efficacy of first line drug treatments (ie. Copaxone or Tecfidera) by altering the metabolic state of the host via calorie restriction with the aim to re-equilibrate immune/inflammatory responses of patients.

Multiple sclerosis (MS) is an autoimmune disorder characterized by central nervous system (CNS) inflammation, demyelination, and axonal damage. Its pathogenesis consists of an initial T cell priming against myelin antigens in secondary lymphoid organs (induction phase) followed by migration of auto-reactive T cells and other immune system cells through the blood brain barrier into the CNS (effector phase). MS attacks are self-limiting, illustrating the existence of a regulatory network in which regulatory T cells (Treg) play a key role. Treg cells, which comprise 5%-10% of peripheral cluster of differentiation (CD)4+ T cells, inhibit effector T cell responses and can suppress MS. One of the immune abnormalities observed in MS is a reduction in the number and suppressive functions of Tregs. Furthermore, an abnormal Treg proliferation and metabolic profile was described in MS patients characterized by altered interleukin (IL) 2- IL 2 receptor - STAT5 signaling, and activation of the mammilian target of rapamycin (mTOR) metabolic pathway. More recently, the risk of MS has been associated with several environmental factors, including obesity and diet. Current treatments are only partially effective in controlling disease activity in relapsing-remitting (RR)-MS patients and no drugs are available that prevent or slow the progressive forms of MS. There remains an urgent need for new and safe therapies for patients that do not respond optimally to current drug treatments. In recent times, it has become evident that the control of orexigenic and anorexigenic circuits not only affects the regulation of body weight but also dramatically influences other important physiological and dominant functions, including immune homeostasis. In particular, several cytokines, hormones, neuropeptides and transcription factors play relevant roles in both metabolism and immunity. It has been shown that dietary intervention can alter autoimmune disease progression, indeed dietary indoles suppress delayed-type hypersensitivity by inducing a switch from pro-inflammatory Th17 cells to anti-inflammatory Treg cells. Recent reports have shown that caloric restriction (CR) can significantly increase the survival and reduce clinical progression in EAE. CR induces multiple metabolic and physiologic modifications, including anti-inflammatory, antioxidant, and neuroprotective effects that could be beneficial in MS. A recent report has shown that dietary restriction improves repopulation but impairs lymphoid differentiation capacity of hematopoietic stem cells in early aging, by inhibiting the proliferation of lymphoid progenitors, resulting in decreased production of peripheral B lymphocytes and impaired immune function. Moreover prolonged fasting (PF) or a fasting mimicking diet (FMD) lasting 2 or more days have been shown to increase protection of multiple systems against a wide variety of chemotherapy drugs; PF or FMD reverses the immunosuppression or immunosenescence effects of either chemotherapy or aging by a hematopoietic stem cell-based regenerative process. Chronic CR, a ketogenic diet (KD) and intermittent fasting have been shown to prevent EAE, reducing inflammation, demyelination, and axon injury - without suppressing immune functions, when administered prior to disease induction or signs. CR associates with increased plasma levels of corticosterone and adiponectin, and with reduced concentrations of IL-6 and leptin. The effects of CR in EAE in the monophasic Lewis rat model show that upon calories restriction by 33% or 66%, EAE can be totally inhibited in the latter group, in which a depressed immune function with fewer T cells in lymphoid organs, impaired proliferation and cytokine production are observed. CR could benefit EAE through multiple metabolic and cytokine/adipokine changes that ultimately lead to a reduced inflammatory response. Other possibilities include CR-associated increase in ghrelin, neuropeptide Y (NPY) and endocannabinoids - all of which can dampen EAE and are increased during CR and starvation. Environmental factors are believed to play a role in the pathogenesis of MS, which is more prevalent in the Western world, where increased intake of saturated fats of animal origin is common. Although there has been speculation that diet may alter the course of MS, only a few randomized, controlled studies of dietary alterations in autoimmunity have been published, and none involving CR. Yet, dietary intervention might be attractive in MS, i.e. with CR associated with adequate nutrition, which can be safely accomplished through proper monitoring and could provide additional benefits such as improved insulin sensitivity, lower low-density lipoprotein, cholesterol, blood pressure and, importantly, reduced inflammation. In conclusion, in spite of the above robust experimental evidence, no specific studies have been performed to dissect at cellular level the mechanism of action of CR in the context of autoimmunity and MS. This study aims at investigating this specific point to pave for a wider utilization of the nutritional approach to alter MS progression and activity to be associated to first line drug treatments. Rationale and specific aims. Several disease modifying drugs are approved for RR-MS treatments and have shown to reduce relapse rates by modulating immune responses; however, their impact on long-term disease progression and accrual of irreversible neurological disability remains largely unclear, underlining the need for novel therapeutic strategies. The aim of this pilot study is to investigate the cellular and molecular mechanism of action of metabolic manipulation through CR accompanied or not to removal of specific antigenic foods (gluten/cow's milk) and their impact on RR-MS progression during treatment with conventional first line drugs. the objective of this study is to improve the outcome of RR-MS and the efficacy of first line drug treatments (either dimethyl fumarate or glatiramer acetate) by altering the metabolic state of the host via a mild CR (15-20% caloric restriction of the ideal diet for the individual) accompanied or not to removal of specific foods from diet (gluten and cow's milk derivatives), with the aim to re-equilibrate immune/inflammatory responses of the patients. Specifically, will be analyzed the following read outs in patients before and after specific treatments: Aim 1) The impact of CR on the immunophenotype of different subclasses of circulating immune cells from the blood of RR-MS patients, and its correlation with the clinical status of the patients (ie. disease duration, number of relapses since onset, grade of disability and severity based on expanded disability status score (EDSS), MS severity score (MSSS) as well as presence of disease activity based on MRI imaging (gadolinium enhancing lesions) and overall lesion burden (T2 lesion volume)), and immuno-metabolic parameters (ie. circulating leptin, adiponectin, adipokines, etc); Aim 2) The capacity of CR to affect T cell and regulatory T cell function/activity (activation, proliferation, suppression, Foxp3 induction) and molecular signalling pathway involved and possibly altered upon T-cell receptor (TCR) stimulation (ERK-mTOR-p27kip1 etc); Aim 3) The effect of CR on the metabolic asset of circulating T cell populations (ie. measurement of glycolysis, oxidative phosphorylation and fatty acid oxidation); Aim 4) The advanced proteomic profile, including protein modifications such as phosphorylation, acetylation, methylation, ubiquitination and glycosylation in conventional T cells and Treg cells from RR-MS subjects; Aim 5) The effect of CR on the composition of the intestinal microbiota in RR-MS patients. Patients will be enrolled at diagnosis before starting "first line" drug treatment (either Tecfidera or Copaxone). After starting pharmacological treatments, patients will be randomized in the following 3 groups: 1. 40 naive to treatment RR-MS (30 on Tecfidera + 10 Copaxone treatment) Free Diet Controls (FD); 2. 40 naive to treatment RR-MS (30 on Tecfidera + 10 Copaxone treatment) on mild Caloric Restriction (15-20% caloric restriction); 3. 40 naive to treatment RR-MS (30 Tecfidera + 10 Copaxone treatment) on mild Caloric Restriction as above in which Cow's Milk and its derivatives and Gluten have been removed (15-20% caloric restriction- plus excluding from diet cow's milk, its derivatives and gluten). The patients will be enrolled in 10-12 months and followed for 24 months. Each group will have an equal distribution in age, gender and body mass index. Blood samples for the cellular, molecular and metabolic assessment of immune cells as well as the flow-cytometric extended analyses and proteomics will be obtained at baseline (T0), months 6 (T1), months 12 (T2) and months 24 (T3) after baseline. Besides the immunological studies, blood aliquots will be used for routine blood tests to control for concomitant infections. For the same purpose, urinalysis will be obtained at each time point. MRI scans will be performed for clinical practice at screening (Visit 0) and at months 6 (Visit 2), months 12 (Visit 3) and months 24 (Visits 4).