Intravenous Immunoglobulin Treatment in Multifocal Motor Neuropathy
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Multifocal motor neuropathy (MMN) is characterized by asymmetric weakness of limbs and the electrophysiological finding of conduction block in motor nerves. Conduction block is the inability of nerves to propagate action potentials and is probably caused by immune-mediated dysfunction of the axon at the nodes of Ranvier or the myelin sheath. MMN immune pathogenesis has not been elucidated.
In approximately 50% of all patients, IgM antibodies that bind to the glycolipid GM1, which is abundantly expressed in peripheral motor nerves, can be detected. A recent study showed an association with HLA-DRB1*15, and virtually all patients respond to treatment with intravenous immunoglobulin (IVIG) in at least the early stages of the disease.
This review aims at providing a concise overview of what is known about MMN pathogenesis, and how the beneficial effect of IVIG might be explained.
KeywordsMultifocal motor neuropathy intravenous immunoglobulin conduction block GM1 antibodies
Clinical Picture of MMN
Asymmetric weakness of distal arm muscles without sensory deficits is a highly uncommon presentation for a peripheral neuropathy. Until its first detailed description in 1988 , multifocal motor neuropathy (MMN) was often diagnosed as amyotrophic lateral sclerosis (ALS) with a surprisingly benign disease course. ALS is a neurodegenerative disorder caused by degeneration of motor neurons in the anterior horn of the spinal cord and upper motor neurons in the central nervous system (CNS). Unlike ALS, which has a poor prognosis with a median survival of approximately 3 years, patients with MMN have a normal life expectancy, with gradual or stepwise progressive weakness of muscles in the distal arm and leg or a stable disease course after onset [2, 3].
Proposed Diagnostic Criteria for MMN
1. Slow or stepwise progressive limb weakness
2. Asymmetrical limb weakness
3. Fewer than 7 affected limb regions (upper/lower arm, upper/lower leg on both sides, maximum 8)
4. Tendon reflexes in affected limbs are decreased or absent
5. Signs and symptoms are more pronounced in arms than in legs
6. Age 20-65 years at onset of disease
7. No objective sensory abnormalities except for vibration sense
8. No bulbar signs or symptoms
9. No upper motor neuron features
10. No other neuropathies
1. CSF protein <1 g/L
2. High anti-GM1 IgM titer
3. High signal intensity on T2-weighted MRI of the brachial plexus
1. Definite motor conduction block: CMAP area reduction on proximal versus distal stimulation of at least 50% over a long segment (between erb and axilla, upper arm, lower arm, lower leg), or a CMAP amplitude reduction on proximal versus distal stimulation of at least 30% over a short distance (2.5 cm) detected by inching. CMAP amplitude on stimulation of the distal part of the segment with motor conduction block of at least 1 mV
2. Probable motor conduction block: CMAP amplitude reduction on proximal versus distal stimulation of at least 30% over a long segment of an arm nerve. CMAP amplitude on stimulation of the distal part of the segment with motor conduction block of at least 1 mV
3. Slowing of conduction compatible with demyelination: MCV 75% of the lower limit of normal; DML or shortest F wave latency 130% of the upper limit of normal or absence of F waves all after 16-20 stimuli. CMAP amplitude on distal stimulation of at least 0.5 mV
4. Normal sensory nerve conduction in arm segments with motor conduction block. Normal SNAP amplitudes on distal stimulation
1-11 on clinical criteria, 1 on laboratory criteria, 1 and 4 on electrodiagnostic criteria
1-3 and 6-11 on clinical criteria, 1 on laboratory criteria, 2 and 4 on electrodiagnostic criteria
1 and 7-11 on clinical criteria, 2 or 3 on laboratory criteria, 3 and 4 on electrodiagnostic criteria
Conduction Block and Nerve Pathology
The underlying mechanisms of nerve dysfunction and, in particular, CB in patients with MMN are incompletely understood. CB could be caused by dysfunction of the axon or the myelin sheath, but the scarce pathological studies of motor nerves are equivocal, showing both signs of demyelination  and axonal degeneration . Electrophysiological studies have confirmed that axonal degeneration is common in MMN [6, 7] and that it is the most important determinant of permanent weakness .
Nerve excitability studies have been used to address whether CB is caused by depolarizing or hyperpolarizing mechanisms but have yielded inconsistent results. Hyperpolarization, depolarization, and combinations have been described [6, 8]. Depolarizing CB may precede hyperpolarizing CB in the course of MMN, but these findings remain to be confirmed . Importantly, axonal dysfunction in MMN may be more widespread than solely at the site of CB; this is possibly due to Na+ channel dysfunction . Axonal dysfunction decreased after treatment with IVIG, which suggest underlying immune-mediated mechanisms. A groundbreaking experimental study using a rabbit model for acute motor axonal neuropathy (AMAN) has provided important insight into how antibodies against GM1 disrupt the architecture of Na+ channel clusters at the nodes of Ranvier . By analogy, this study has offered important clues as to how immunological and electrophysiological features of MMN are linked.
Anti-Ganglioside Antibodies and MMN
The presence of serum IgM antibodies against GM1 was acknowledged in the first description of MMN  and has been since confirmed by many studies. Although the reported prevalence of IgM antibodies against GM1 in MMN patients varies widely, probably due to differences in laboratory assays [2, 3], these antibodies can be detected in serum samples from approximately half of all MMN patients. GM1 is a glycolipid from the family of gangliosides, which consist of a ceramide anchor coupled to a varying number of oligosaccharide residues and sialic acids .
Although gangliosides are abundantly expressed in nervous tissues, their biological functions are not completely understood. From the 1980s, it is becoming increasingly clear that gangliosides are important targets for antibodies in immune-mediated neuropathies, in particular AMAN, the extensively studied pure motor axonal variant of Guillain-Barré syndrome (GBS). The gangliosides GM1 and GD1a are especially abundant in motor nerves, and antibodies from all major isotypes (IgM, IgG, IgA) against these gangliosides are detected in serum from AMAN patients. These antibodies are elicited by infection with microorganisms expressing ganglioside-like mimics on their surface (a process called molecular mimicry) a few days or weeks prior to disease onset . Similarly, experimental exposure to gangliosides or bacterial constituents exposing ganglioside-like structures induces inflammatory neuropathy in rabbits and humans . Anti-ganglioside IgG antibodies were shown to induce inflammation and to disrupt nerve function by activating complement and leukocytes after binding to their targets .
Origin of Anti-GM1 IgM Antibodies in MMN Patients
The presence of anti-GM1 IgM antibodies in serum from almost 50% of patients with MMN seems to suggest an activation of GM1-specific B cells. Assuming that these antibodies contribute to the etiopathogenesis of MMN and are not secondary to the release of gangliosides from damaged axons, elucidation of the mechanism of GM1-specific B-cell activation may provide clues for alternative treatment strategies. GM1-specific B cells may be activated by infections (molecular mimicry), intrinsic B-cell clone changes (monoclonal gammopathy), or by autoimmune mechanisms.
The almost exclusive presence of IgM and the results from serological studies, which indicate that few MMN patients had infections with the GM1-mimic expressing Campylobacter jejuni , do not support pathogenic similarities with AMAN. The hypothesis that MMN is a postinfectious or parainfectious disorder may be hard to investigate. The chronic disease course in MMN may cause bias in recall of individual infectious histories, and maintenance treatment with IVIG complicates the interpretation of serological studies; thus, excluding methodology that has been pivotal in the dissection of GBS pathogenesis . Although monoclonal gammopathy has been observed in patients with MMN, it cannot be detected by immunofixation in the large majority of patients [2, 3]. Monoclonal gammopathy of GM1-specific B cells does not, therefore, offer a satisfactory explanation for MMN in the majority of patients.
It is not clear also whether MMN is a classic autoimmune disease. Although the overrepresentation of male patients may argue against autoimmune disease, we observed a clear association of MMN with the HLA-DRB1*15 allele in a case-control study of 74 patients with MMN and 700 controls. Interestingly, this association is also reproducibly found in patients with multiple sclerosis, a multifocal demyelinating disease of the CNS . This association may suggest pathogenic similarities with multiple sclerosis and provide a new clue for MMN pathogenesis, i.e., a contribution of antigen-presenting cells (APC). APC are pivotal in triggering adaptive immune responses by presenting autoantigens to T cells or B cells. Glycolipids are not presented by APC in an HLA-restricted fashion but by HLA-like molecules from the CD1 family. Polymorphisms of CD1 molecules were not found to be associated with MMN . The association with HLA-DRB1*15 was independent of the presence of anti-GM1 IgM antibodies. This may, therefore, suggest the existence of as yet unidentified autoantigens or indicate the presence of genetic risk factors that are in linkage disequilibrium with the HLA-DRB1*15 allele.
The latter possibility may be supported by the lack of evidence for T-cell involvement in MMN. Lymphocytic infiltrates were absent  or minute  in pathological studies, and serological studies have failed to show increased levels of T-cell activating interleukins (IL) such as IL-2 . This is compatible with the notion that glycolipids are T-cell independent antigens and that B cells are the major culprits in the majority of immune-mediated polyneuropathies including MMN.
Treatment of MMN: Present and Future
Treatment trials have uncovered a unique pattern of responsiveness to immune modulatory treatment in MMN. Treatment with IVIG has been shown to be beneficial in randomized controlled trials. Cyclophosphamide has been reported to be effective, but its toxicity precludes long-term use, which is usually necessary in patients with MMN. Plasma exchange and prednisone are well-established therapies in other immune-mediated neuropathies, but have not been shown to be effective in patients with MMN and may even aggravate symptoms [2, 3]. This pattern supports the crucial role of B cells, antibodies, and complement in MMN pathogenesis. Cyclophosphamide is an efficient B-cell inhibiting drug. IVIG may have multiple effects on the humoral part of the immune system of MMN patients, which all contribute to its beneficial effect . First, IVIG may exert anti-idiotypic effects that reduce levels of circulating anti-GM1 IgM antibodies and interfere with B-cell receptors on GM1-specific clones. Second, IVIG may induce inhibitory receptors on B cells as has been shown in patients with chronic inflammatory demyelinating polyneuropathy . Finally, IVIG may interfere with anti-GM1 IgM-mediated complement deposition in nerves . Despite IVIG effectiveness, most patients with MMN experience mild progression of weakness during IVIG maintenance treatment of many years, which can be attributed to axonal degeneration . Although IVIG maintenance treatment in an early stage of the disease may postpone the occurrence of permanent axonal damage , it is not known which dose and treatment would be optimal. In addition to studies that would optimize IVIG treatment strategies for patients with MMN, experimental studies suggest that add-on therapy with B-cell and complement-specific agents might be successful. Anecdotal reports of the long-lasting effects of B cell-specific anti-CD20 monoclonal antibodies (rituximab) call for a randomized trial. Specific inhibitors of the complement system may represent alternative candidates [12, 14], because they might prevent permanent axonal damage. But they also may increase the risk of severe bacterial infections.
MMN is a rare immune-mediated neuropathy that responds to IVIG therapy. Although its pathogenesis is not completely understood, the available data strongly suggest a role for B cells, IgM antibodies, and complement. Further dissection of its etiology may help to select effective treatment modalities. Future treatment strategies should aim ultimately at preventing permanent axonal damage without increasing the risk of serious side effects.
Elisabeth A. Cats is supported by a grant from the Prinses Beatrix Fonds.
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