Emerging therapies for treatment of multiple sclerosis

Abstract

In the last decade, a new armamentarium of immune-based therapies have been developed and tested in patients with multiple sclerosis. Some of these therapies are showing a high level of efficacy, with an acceptable adverse effect profile. Because present therapies have significant limitations in slowing disease progression, require injections, are sometimes associated with significant side effects of immunosuppression, and do little to reverse disability, identifying more effective treatments is an important goal for clinical research in multiple sclerosis. However, in order to improve our current approach to disease-modifying therapies, it is imperative to promote the development of individualized therapy strategies.

Keywords:

• multiple sclerosis
• lymphocyte-targeted therapy
• immune sequestration
• non-specific immune modulation

Introduction

Recent advances in our understanding of the immunopathogenesis of multiple sclerosis (MS) have generated the development of novel and promising neurotherapeutic strategies. This review summarizes the most updated data from recent Phase II/III clinical trials evaluating the clinical efficacy and safety of promising therapeutic interventions in MS patients (Table 1). Other potential side effects may come to light with more patients studied and greater use of these drugs.

Table 1 Selected emerging MS therapies

Lymphocyte-targeted therapy	Mechanism of action	Route/Dose	Results	Status	AEDs
Cladribine	Purine nucleoside analog	Oral (3.5 and 5.25 mg/kg total dose)	58% ↓ RR, 43% disease free	Phase III	HZV, lymphopenia, HA, nasopharyngitis, lymphopenia
Alemtuzumab	Anti-CD52	IV 12 mg dose/y	75% ↓ SAD (12 mg dose), 74% ↓ RR	Phase III	ITP (3 pts), Graves disease (20%)
Daclizumab	Anti-CD25/anti-IL2	SQ 2 mg/kg (Q2w)	72% ↓ CEL in RRMS patients	Phase II	Skin rash, chest discomfort, headaches, lymphopenia
Rituximab	Anti-CD20	IV (1 gram dose, Q2w, × 2)	91% ↓ CEL in RRMS	Phase II	Infusion reaction, allergies
CTLA4Ig	Prevents T cell activation	IV (2, 10.0, 20.0, or 35.0 mg/kg)	No significant changes	Phase I	Lymphadenopathy, urinary tract infections, headaches, blurred vision, and upper respiratory tract infections
Immunesequestration
Fingolimod	Sphingosine-1-phosphate (S1P) analog	Oral (1.25 and 5 mg)	80% ↓ CEL, 50% ↓ RR	Phase III	Bradycardia, nasopharyngitis, dyspnea, headaches, diarrhea, nausea, encephalitis, skin cancer
SB-683699	Alpha-4 integrin antagonist	Oral (150–1200 mg Twice Daily)	No data available	Phase II	No data available
Unspecific immunosupression
Laquinimod	Antiinflammatory	Oral 0.6 mg/d	40% ↓ CEL	Phase III	LFT elevation, Budd Chiari
Fumaric acid (BG12)	Antiinflammatory/Neuroprotective	Oral (120–240 mg TID)	69% ↓ CEL	Phase III	Diarrhea, cramps, nausea and flushing
Teriflunomide	Inhibition of immune cell proliferation	Oral (7 and 14 mg dose)	61% ↓ CEL	Phase II	Nasopharyngitis, alopecia, nausea, limb pain, diarrhea, and arthralgia

Abbreviations: RR, relapse rate; HZV, herpes zoster virus; HA, headaches; IV, intravenous; SAD, sustained acumulation of disability; ITP, immune thrombocytopenic purpura; SQ, subcutaneous; CEL, contrast enhancing MRI lesions; RRMS, relapsing remitting Multiple Sclerosis; LFT, liver function test.

Lymphocyte-targeted therapy

Cladribine

Cladribine is a purine nucleoside analogue that produces lymphotoxic effects when incorporated into the DNA of resting and dividing cells with high deoxycytidine kinase activity (lymphocytes and monocytes), and subsequent interruption of DNA replication, DNA damage, and cell death.¹ In addition to its lymphotoxic effects, cladribine possesses epigenetic properties, by inhibiting S-adenosyl homocysteine hydrolase and DNA methylation.² It received FDA approval in the 1980s for treatment of hairy cell leukemia.

Parenteral cladribine (total dose 2.8 mg/kg) significantly reduced the number and volume of T₁ gadolinium-enhancing lesions, accumulation of T₂ lesion volume, relapse rate, and disability progression in patients with progressive and relapsing forms of MS.^3–5 A dose-dependent increase in adverse events was observed, leading to selection of low doses for use in an ongoing clinical development program of an oral tablet formulation.

A recent placebo-controlled Phase III trial using oral cladribine in patients with relapsing-remitting MS (RRMS), showed a 58% reduction in annualized relapse rates (3.5 mg/kg daily for four to five days, with two courses in the first year) at two years compared with placebo. In addition, 80% of patients remained relapse-free, compared with 61% of patients in the placebo group (P < 0.001 for both dose regimens). Patients in the active drug group experienced a 30% reduction in the risk of disability progression relative to patients in the control group.⁶ Adverse events included headaches, nasopharyngitis, upper respiratory tract infections, and nausea. Lymphopenia occurred more frequently in the active drug group (22%). Of the patients treated with cladribine tablets, 2.3% reported herpes zoster infections, although these were localized to the skin and were responsive to preventative treatment. A Phase III trial investigating oral cladribine in clinically isolated syndrome and a Phase IIb trial of combination therapy with interferon (IFN) β-1a is currently underway with an estimated date for completion of February 2010. Cladribine has the potential to be the first orally administered disease-modifying therapy available for patients with relapsing MS. As of December 2009 the FDA has not accepted Serono’s approval application.

Alemtuzumab

Alemtuzumab is a humanized monoclonal antibody directed against CD52, a cell surface receptor expressed on lymphocytes, natural killer cells, monocytes, and macrophages. Alemtuzumab binds to B- and T- lymphocytes, resulting in antibody-dependent cell lysis, and subsequent elimination from the bone marrow and blood, with the effect lasting up to 16 months. Interestingly, the capacity of the immune cells to regenerate remains intact after repetitive drug cycles, but immature forms of B-cells (transitional type I cells) possibly driven by high B-cell activation factor levels are seen early in the course of immune reconstitution. This event could explain the association and development of antibody-mediated autoimmune disorders seen in the course of alemtuzumab therapy. Alemtuzumab is currently FDA-approved to treat B-cell chronic lymphocytic leukemia.

Studies of alemtuzumab in the treatment of patients with relapsing-remitting (RR) and secondary progressive MS (SPMS) have suggested efficacy in the suppression of annualized relapse rates, but with variable results in preventing progression of disability, depending on stages of the disease. In a recent Phase II randomized blinded clinical trial of intravenous (IV) alemtuzumab at 12 mg per day or 24 mg per day for five consecutive days during the first month and on three consecutive days at 12 and 24 months, alemtuzumab significantly reduced the rate of sustained accumulation of disability by 71%, with a 74% reduction in the annualized rate of relapse compared with IFN β-1a in patients with early RRMS. Over 80% of patients receiving alemtuzumab remained relapse-free at 36 months. Reduction in T₂ lesion volume and total brain volume analysis was greater in the alemtuzumab group. Adverse events in the alemtuzumab group included autoimmune thyroid disorders and thrombocytopenic purpura as well as infections. About one-third of patients develop antibodies against the thyrotropin receptor and subsequently develop autoimmune hyperthyroidism.⁷ Currently there are two Phase III trials comparing two annual cycles of IV alemtuzumab with three times weekly IFN β-1a in treatment-naïve patients with RRMS (CARE-MS1 and CARE MS-2). These studies are expected to be completed in 2011 or 2012.

Rituximab

Rituximab is a chimeric antibody directed against human CD20 phosphoprotein present on all B-cell lineages except for stem cells, pro-B cells, and plasma cells. Rituximab acts by binding to B-cell lymphocytes, initiating a cascade of events that leads to B-cell lysis and subsequent depletion. The benefit of B-cell depletion in controlling the course of the disease supports the recently recognized active role of B-cells in the pathogenesis of MS. The standard dose of rituximab is 375 mg/m² given weekly for four weeks, or a fixed dose of 2 g divided into two infusions of 1 g each two weeks apart. Following an IV administration of 2 g of rituximab, CD20 positive B-cells are rapidly depleted and remain undetectable for up to six months longer.

Rituximab has shown efficacy in the treatment of patients with RRMS. A recently completed randomized clinical trial using a standard dose of rituximab in RRMS patients demonstrated a 91% reduction in the number of gadolinium-enhancing lesions on (magnetic resonance imaging (MRI) scans, as well as a significant reduction in the number of clinical relapses. Mild infusion-related complications were seen in most patients, but serious adverse reactions were rare.⁸ In a recent trial of patients with primary progressive multiple sclerosis (PPMS), rituximab appeared to have efficacy only in young patients with signs of active inflammation on MRI scans.⁹ Five cases of progressive multifocal leukoencephalopathy have been recently reported in patients receiving rituximab for the treatment of rheumatoid arthritis and systemic lupus erythematosus. However, these patients were receiving other immunosuppresants.

Ocrelizumab, a humanized monoclonal antibody against human CD20, is currently under investigation in a Phase II trial evaluating its efficacy and safety in patients with RRMS. The estimated date of completion for this trial is 2012.¹⁰ Given the functional similarities between rituximab and ocrelizumamb, it is unclear which of these will be developed for use in MS.

Daclizumab

Daclizumab is a humanized mouse monoclonal antibody that binds to the alpha-subunit of the interleukin (IL)-2 receptor. This receptor is present on activated T- and B-cells but not on natural killer (NK) cells, and is crucial for T-cell proliferation and activation. The clinical benefit of daclizumab has been linked to significant expansion of immunoregulatory CD56 NK cells, and subsequent downregulation of adaptive T-cell responses (CD4 and CD8 positive T-cells).¹¹ In an initial open-label study with IV daclizumab 1 mg/kg, five patients with SPMS and six patients with RRMS demonstrated a decrease in number of contrast-enhancing lesions by 78% and in relapse rate by 81% compared with baseline.¹² A recent open-label Phase II trial using subcutaneous daclizumab 2 mg/kg in MS patients with inadequate response to IFN β therapy, demonstrated a 72% reduction in the number of new or enlarged contrast-enhancing lesions at week 24 compared with patients receiving IFN β alone. Because Type I IFN is also known to enhance NK cell function, the question of possible synergism between IFN and daclizumab therapy is raised.¹³ Skin rash, chest discomfort, headaches, lymphopenia, generalized lymphadenopathy, and transient elevation of liver function tests and bilirubin levels have been reported. Daclizumab is already in clinical use to prevent rejection of kidney transplants. A multicenter Phase II trial investigating a subcutaneous formulation of daclizumab monotherapy is ongoing.

CTLA-4 Ig

CTLA-4Ig is a chimeric fusion protein that prevents T-cell activation by binding the B7-1 and B7-2 costimulatory molecules on antigen-presenting cells. A recent Phase I clinical trial showed that IV administration of CTLA-4Ig was well tolerated in patients with MS, and most adverse events were rated as mild. Lymphadenopathy, urinary tract infections, headaches, blurred vision, and upper respiratory tract infections were most frequently reported. Immunologic assessment of the patients showed a reduction in myelin basic protein proliferation within two months of infusion and decreased IFN-γ production by myelin basic protein-specific lines. No significant changes in clinical or MRI parameters were observed during the study.¹⁴

Immune sequestration

Fingolimod

Fingolimod (FTY720), an oral sphingosine-1-phosphate (S1P) analog, acts as a partial agonist on S1P receptors, inducing internalization of the S1P receptor, thereby blocking the mechanism necessary for lymphocytes to migrate out of secondary lymphoid structures. Fingolimod is associated with significant decreases in circulating T- and B-cells, particularly in central and naïve memory T-cells, with lesser reductions on effector memory T-cells.¹⁵ As a result of its lipophilic nature, fingolimod crosses the blood-brain barrier and possibly also downmodulates S1P1 in neural cells and astrocytes, thereby reducing astrogliosis, a phenomenon associated with neurodegeneration in MS.¹⁶

A recent multicenter, randomized, double-blind, placebo-controlled Phase III study with extension in RRMS patients demonstrated that oral fingolimod at doses of 1.25 and 5 mg, reduced the number of new focal inflammatory lesions by 80% and relapse rates by 50% compared with placebo.⁹ Over two years, the average annualised relapse rate in patients receiving fingolimod was 0.21, 75%–77% of patients remained free of relapses, and 80% remained free of new enhancing MRI lesions. In addition, patients initially receiving placebo showed a marked improvement in clinical parameters of MS after switching to fingolimod in the extension study, which was sustained at month 24. Adverse reactions included bradycardia, nasopharyngitis, dyspnea, headaches, diarrhea, and nausea. Initial bradycardia was seen more frequently in the 5 mg dose group. Three cases of basal cell carcinoma, three of squamous cell carcinoma, and one of melanoma were reported. Two fatalities occurred during the trial, and were associated with chicken pox and herpes virus infection. In addition, a single case of hemorrhagic encephalitis was reported but with an unclear causal relationship. Ongoing Phase III trials comparing the safety and efficacy of oral fingolimod 0.5 mg and 1.25 mg with IFN β-1a will soon yield results.¹⁷

SB-683699

SB-683699 is an oral medication that is thought to inhibit leukocyte trafficking across the blood-brain barrier by antagonism of alpha-4 integrins. A Phase II trial was recently completed in patients with RRMS evaluating the safety and efficacy of SB-683699 (150–1200 mg twice daily) in the development of MRI-confirmed new brain lesions at six months. Data from that trial will be available soon.¹⁸

Non-specific immune modulation

Laquinimod

Laquinimod (quinoline-3-carboxamid) is a once-daily, orally administered immunomodulatory compound that is being developed as a disease-modifying treatment for RRMS. The anti-inflammatory properties of laquinimod are thought to be secondary to downregulation of major histocompatibility complex Class II gene transcription factors, stimulation of neurotrophin-3, neurotrophin-4 and brain-derived neurotrophic factor, activation of the anti-inflammatory IL-4 pathway in CD4+ cells, promotion of apoptosis in CD8+ and B-cells, and suppression of the metabolic activity of CD14+ and NK cells. As a consequence, there is a cytokine balance in favor of anti-inflammatory T-helper (Th)-2/Th-3 cytokines, with suppression of proinflammatory and cytokine-related genes. A Phase IIb study in 306 patients demonstrated that an oral daily 0.6 mg dose of laquinimod significantly reduced MRI disease activity by a median of 60% versus placebo in RRMS patients. The majority of the patients that have participated in this trial are now receiving treatment with laquinimod in an open-label extension trial.¹⁹ An ongoing Phase III trial is currently evaluating the efficacy of laquinimod 0.6 mg daily in patients with RRMS, with an estimated completion date of 2010.²⁰

Laquinimod appears to be well tolerated, with only transient and dose-dependent increases in liver enzymes. A case of Budd-Chiari syndrome occurred after one month of exposure in a patient with underlying hypercoagulability. Unlike its precursor substance, linomide, no cases of serositis or myocardial infarction have been reported so far in patients receiving laquinimod.

BG00012

BG00012 is an oral formulation of dimethyl fumarate that may exert a combination of anti-inflammatory and neuroprotective biological effects. Although its exact mechanism of action is not known, BG00012 is thought to inhibit immune cells by stimulating the expression of anti-inflammatory cytokines, such as IL-10, IL-4, and IL-5. Hence, it is thought that dimethyl fumarate can induce a shift from a Th-1 (pro-inflammatory) to a Th-2 (anti-inflammatory) T-cell response.²¹ In addition, BG00012 may have a neuroprotective therapeutic effect by inducing Phase II detoxification genes and upregulation of the Phase II detoxification enzyme, NAD(P)H:quinone oxidoreductase-1.²²

A previous multicenter, controlled clinical trial of oral BG00012 involving 257 people with RRMS receiving various doses of BG00012 capsules or placebo showed a dose-dependent reduction in active inflammation on MRI scans.²³ Tolerability was good overall, with adverse events, including abdominal pain and flushing, more commonly occurring in the active treatment group. Two Phase III trials are currently ongoing evaluating if BG00012 is effective in reducing the proportion of relapses, decreasing the number of brain lesions, and slowing time to progression (DEFINE and CONFIRM). The estimated completion date for both studies is December 2010.

Teriflunomide

Teriflunomide is an inhibitor of mitochondrial dihydroorotate dehydrogenase, an enzyme critically involved in pyrimidine synthesis. Because activated lymphocytes largely depend on de novo pyrimidine synthesis, pyrimidine depletion might result in inhibition of immune-cell proliferation.²⁴ There is some evidence from in vitro studies suggesting that teriflunomide induces Th-2-mediated anti-inflammatory cytokine activation.

Oral teriflunomide was tested in a randomized, double-blind, placebo-controlled Phase II study. Patients with relapsing forms of MS were randomized to receive placebo, teriflunomide 7 mg or 14 mg a day for 36 weeks. Teriflunomide demonstrated a dose-dependent reduction in the number of T₁-enhancing lesions. Teriflunomide was generally safe and well tolerated. Adverse effects included nasopharyngitis, alopecia, nausea, limb pain, diarrhea, and arthralgia. Hepatic necrosis and pancytopenia have been reported in patients with rheumatoid arthritis taking teriflunomide.

A two-year, double-blind, placebo-controlled Phase III study in relapsing MS is in progress.²⁵ The primary outcome measure is relapse rate. Other ongoing or planned studies of teriflunomide include a Phase II study of combination with IFN-β, a Phase II study of combination with glatiramer acetate, and a placebo-controlled Phase III trial in clinically isolated syndrome.^26–28

Failed trials

Antigen-based immune therapies

Induction of tolerance by antigen-based immune therapy appears to be a promising strategy in the treatment of autoimmune disorders. Recent studies evaluating the administration of a myelin basic protein-derived peptide (MBP8298) in patients with progressive forms of MS suggested a benefit in disease progression by clinical parameters in a subgroup of patients with HLA-DR2 and DR4 haplotypes. Two Phase II/III trials investigating MBP9298 in SPMS and RRMS patients with HLA-DR2 and four haplotypes were unfortunately negative.^29,30 As of December 2009 there are no plans to restudy this molecule.

IL-12 and IL-23 inhibitors

IL-12 and IL-23 have been strongly implicated in the pathogenesis of MS. IL-23 is produced mainly by activated myeloid cells, and promotes and stabilizes IL-17 production by CD4+ T-cells, with subsequent tissue inflammation. Circulating mononuclear cells from patients with MS express increased concentrations of IL-12 and IL-23. Ustekinumab is a fully human monoclonal antibody against IL-12/23 p40 that neutralises IL-12 and IL-23. A Phase II, multicentre, randomised, double-blind, placebo-controlled study was done evaluating the administration of 27 mg, 90 mg, or 180 mg ustekinumab every four weeks or 90 mg ustekinumab every eight weeks versus placebo. Unfortunately, this study did not demonstrate a significant benefit on formation of inflammatory white matter lesions or affect clinical events in patients with RRMS.³¹

Atacicept

Atacicept is an immunoglobulin fusion protein tumor necrosis factor family receptor transmembrane activator, calcium modulator, and cyclophilin ligand interactor which sequesters the B-cell survival factor, a proliferation-inducing ligand (APRIL), and B-lymphocyte stimulator of the tumor necrosis factor family (BLys) and thus inhibits later stages of B-cell development. A recent Phase II clinical trial evaluating efficacy and safety profiles in patients with MS was terminated because preliminary data suggested an increase in disease activity in patients receiving atacicept.³²

Remyelination and neural repair

CNS remyelination is mostly mediated by oligodendrocyte progenitor cells. The ability to remyelinate is in general incomplete and fails over time. Many environmental factors play an important role in promoting or inhibiting myelin repair and oligodendrocyte differentiation. Of these, neurite outgrowth inhibitor Nogo-A, and its co-receptors TROY and LINGO-1 have been studied in both in vitro and in vivo studies.³³ Administration of anti-Nogo-A antibodies resulted in significant axonal growth in vitro and in animal models of spinal cord injury.³⁴ Passive immunization with anti-Nogo-A antibodies in animal models of MS resulted in less demyelination and axonal damage compared with controls.³⁵ A Phase I clinical open-label multicenter safety study evaluating continuous intrathecal administration of anti-Nogo-A antibody (ATI355) in patients with spinal cord injury is currently ongoing. The completion date is estimated to be November 2010. Overexpression of LINGO-1 inhibits oligodendrocyte differentiation and myelination, whereas attenuation of its function or administration of LINGO-1 antagonist antibody (anti-LINGO-1) enhances oligodendrocyte differentiation and myelination.^36,37 In vivo studies demonstrated the presence of TROY and LINGO-1 in a subpopulation of reactive astrocytes, macrophages, and microglia in MS brain lesions.³⁸ Treatment with an antibody antagonist to LINGO-1 function leads to functional recovery and increased integrity of axons in rats with experimental autoimmune encephalomyelitis induced by myelin-oligodendrocyte-glycoprotein.³⁹ Studies of an anti-LINGO-1 monoclonal antibody are under consideration.

Cellular remyelinating strategies, involving both embryonic and neural stem cells, are being proposed as an elective source of brain cells for transplantation and potential therapies for MS. In vitro studies suggest that neuronal stem cells have the potential to restore neuronal activity and produce new neurons through transdifferentiation. Adult bone marrow-derived stromal cells were shown to induce similar immunomodulatory and neuroregenerative effects in the animal model of chronic experimental autoimmune encephalomyelitis.^40,41 These concepts have led to an interest in the use of stem cells for neuronal regeneration and restoration of neurologic function in MS. To date, there are two clinical trials evaluating the use of autologous stem cells for the treatment of MS in humans.^42,43

Disclosure

Augusto Miravalle, reports no conflicts of interest in this work. John R Corboy reports financial relationships/grant support from: NIH, National MS Society, Juvenile Diabetes Research Foundation, NIAID Immune Tolerance Network, Orasi, Novartis, Eli Lilly and Co, Peptimmune, Genentech.